Friday, 18 February 2011 23:53

Reproductive System: Introduction

Male and female reproductive toxicity are topics of increasing interest in consideration of occupational health hazards. Reproductive toxicity has been defined as the occurrence of adverse effects on the reproductive system that may result from exposure to environmental agents. The toxicity may be expressed as alterations to the reproductive organs and/or the related endocrine system. The manifestations of such toxicity may include:

    • alterations in sexual behaviour
    • reduced fertility
    • adverse pregnancy outcomes
    • modifications of other functions that are dependent on the integrity of the reproductive system.

             

            Mechanisms underlying reproductive toxicity are complex. More xenobiotic substances have been tested and demonstrated to be toxic to the male reproductive process than to the female. However, it is not known whether this is due to underlying differences in toxicity or to the greater ease of studying sperm than oocytes.

            Developmental Toxicity

            Developmental toxicity has been defined as the occurrence of adverse effects on the developing organism that may result from exposure prior to conception (either parent), during pprenatal development or postnatally to the time of sexual maturation. Adverse developmental effects may be detected at any point in the life span of the organism. The major manifestations of developmental toxicity include:

              • death of the developing organism
              • structural abnormality
              • altered growth
              • functional deficiency.

                     

                    In the following discussion, developmental toxicity will be used as an all-inclusive term to refer to exposures to the mother, father or conceptus that lead to abnormal development. The term teratogenesis will be used to refer more specifically to exposures to the conceptus which produce a structural malformation. Our discussion will not include the effects of postnatal exposures on development.

                    Mutagenesis

                    In addition to reproductive toxicity, exposure to either parent prior to conception has the potential of resulting in developmental defects through mutagenesis, changes in the genetic material that is passed from parent to offspring. Such changes can occur either at the level of individual genes or at the chromosomal level. Changes in individual genes can result in the transmission of altered genetic messages while changes at the chromosomal level can result in the transmission of abnormalities in chromosomal number or structure.

                    It is interesting that some of the strongest evidence for a role for preconception exposures in developmental abnormalities comes from studies of paternal exposures. For example, Prader-Willi syndrome, a birth defect characterized by hypotonicity in the newborn period and, later, marked obesity and behaviour problems, has been associated with paternal occupational exposures to hydrocarbons. Other studies have shown associations between paternal preconception exposures to physical agents and congenital malformations and childhood cancers. For example, paternal occupational exposure to ionizing radiation has been associated with an increased risk of neural tube defects and increased risk of childhood leukaemia, and several studies have suggested associations between paternal preconception occupational exposure to electromagnetic fields and childhood brain tumours (Gold and Sever 1994). In assessing both reproductive and developmental hazards of workplace exposures increased attention must be paid to the ppossibleeffects among males.

                    It is quite likely that some defects of unknown aetiology involve a genetic component which may be related to parental exposures. Because of associations demonstrated between father’s age and mutation rates it is logical to believe that other paternal factors and exposures may be associated with gene mutations. The well-established association between maternal age and chromosomal non-disjunction, resulting in abnormalities in chromosomal number, suggests a significant role for maternal exposures in chromosomal abnormalities.

                    As our understanding of the human genome increases it is likely that we will be able to trace more developmental defects to mutagenic changes in the DNA of single genes or structural changes in portions of chromosomes.

                    Teratogenesis

                    The adverse effects on human development of exposure of the conceptus to exogenous chemical agents have been recognized since the discovery of the teratogenicity of thalidomide in 1961. Wilson (1973) has developed six “general principles of teratology” that are relevant to this discussion. These principles are:

                    1. The final manifestations of abnormal development are death, malformation, growth retardation and functional disorder.
                    2. Susceptibility of the conceptus to teratogenic agents varies with the developmental stage at the time of exposure.
                    3. Teratogenic agents act in specific ways (mechanisms) on developing cells and tissues in initiating abnormal embryogenesis (pathogenesis).
                    4. Manifestations of abnormal development increase in degree from the no-effect to the totally lethal level as dosage increases.
                    5. The access of adverse environmental influences to developing tissues depends on the nature of the agent.
                    6. Susceptibility to a teratogen depends on the genotype of the conceptus and on the manner in which the genotype interacts with environmental factors.

                     

                    The first four of these principles will be discussed in further detail, as will the combination of principles 1, 2 and 4 (outcome, exposure timing and dose).

                    Spectrum of Adverse Outcomes Associatedwith Exposure

                    There is a spectrum of adverse outcomes potentially associated with exposure. Occupational studies that focus on a single outcome risk overlooking other important reproductive effects.

                    Figure 1 lists some examples of developmental outcomes potentially associated with exposure to occupational teratogens. Results of some occupational studies have suggested that congenital malformations and spontaneous abortions are associated with the same exposures—for example, anaesthetic gases and organic solvents.

                    Spontaneous abortion is an important outcome to consider because it can result from different mechanisms through several pathogenic processes. A spontaneous abortion can be the result of toxicity to the embryo or foetus, chromosomal alterations, single gene effects or morphological abnormalities. It is important to try to differentiate between karyotypically normal and abnormal conceptuses in studies of spontaneous abortions.

                    Figure 1. Developmental abnormalities and reproductive outcomes potentially associated with occupational exposures.

                    REP040T1

                    Timing of Exposure

                    Wilson’s second principle relates susceptibility to abnormal development to the time of exposure, that is, the gestational age of the conceptus. This principle has been well established for the induction of structural malformations, and the sensitive periods for organogenesis are known for many structures. Considering an expanded array of outcomes, the sensitive period during which any effect can be induced must be extended throughout gestation.

                    In assessing occupational developmental toxicity, exposure should be determined and classified for the appropriate critical period—that is, gestational age(s)—for each outcome. For example, spontaneous abortions and congenital malformations are likely to be related to first and second trimester exposure, whereas low birth weight and functional disorders such as seizure disorders and mental retardation are more likely to be related to second and third trimester exposure.

                    Teratogenic Mechanisms

                    The third principle is the importance of considering the potential mechanisms that might initiate abnormal embryogenesis. A number of different mechanisms have been suggested which could lead to teratogenesis (Wilson 1977). These include:

                      • mutational changes in DNA sequences
                      • chromosomal abnormalities leading to structural or quantitative changes in DNA
                      • alteration or inhibition of intracellular metabolism, e.g., metabolic blocks and lack of co-enzymes, precursors or substrates for biosynthesis
                      • interruption of DNA or RNA synthesis
                      • interference with mitosis
                      • interference with cell differentiation
                      • failure of cell-to-cell interactions
                      • failure of cell migrations
                      • cell death through direct cytotoxic effects
                      • effects on cell membrane permeability and osmolar changes
                      • physical disruption of cells or tissues.

                                           

                                          By considering mechanisms, investigators can develop biologically meaningful groupings of outcomes. This can also provide insight into potential teratogens; for example, relationships between carcinogenesis, mutagenesis and teratogenesis have been discussed for some time. From the perspective of assessing occupational reproductive hazards, this is of particular importance for two distinct reasons: (1) substances that are carcinogenic or mutagenic have an increased probability of being teratogenic, suggesting that particular attention should be paid to the reproductive effects of such substances, and (2) effects on deoxyribonucleic acid (DNA), producing somatic mutations, are thought to be mechanisms for both carcinogenesis and teratogenesis.

                                          Dose and Outcome

                                          The fourth principle concerning teratogenesis is the relationship of outcome to dose. This principle is clearly established in many animal studies, and Selevan (1985) has discussed its potential relevance to the human situation, noting the importance of multiple reproductive outcomes within specific dose ranges and suggesting that a dose-response relationship could be reflected in an increasing rate of a particular outcome with increasing dose and/or a shift in the spectrum of the outcomes observed.

                                          In regard to teratogenesis and dose, there is considerable concern about functional disturbances resulting from the ppossiblebehavioural effects of pprenatal exposure to environmental agents. Animal behavioural teratology is expanding rapidly, but human behavioural environmental teratology is in a relatively early stage of development. At present, there are critical limitations in the definition and ascertainment of appropriate behavioural outcomes for epidemiological studies. In addition it is ppossiblethat low-level exposures to developmental toxicants are important for some functional effects.

                                          Multiple Outcomes and Exposure Timing and Dose

                                          Of particular importance with respect to the identification of workplace developmental hazards are the concepts of multiple outcomes and exposure timing and dose. On the basis of what we know about the biology of development, it is clear that there are relationships between reproductive outcomes such as spontaneous abortion and intrauterine growth retardation and congenital malformations. In addition, multiple effects have been shown for many developmental toxicants (table 1).

                                          Table 1. Examples of exposures associated with multiple adverse reproductive end-points

                                          Exposure Outcome
                                            Spontaneous abortion Congenital malformation Low birth weight Developmental disabilities
                                          Alcohol X X X X
                                          Anaesthetic
                                          gases
                                          X X    
                                          Lead X   X X
                                          Organic solvents X X   X
                                          Smoking X X X  

                                           

                                          Relevant to this are issues of exposure timing and dose-response relationships. It has long been recognized that the embryonic period during which organogenesis occurs (two to eight weeks post-conception) is the time of greatest sensitivity to the induction of structural malformations. The foetal period from eight weeks to term is the time of histogenesis, with rapid increase in cell number and cellular differentiation occurring during this time. It is then that functional abnormalities and growth retardation are most likely to be induced. It is ppossiblethat there may be relationships between dose and response during this period where a high dose might lead to growth retardation and a lower dose might result in functional or behavioural disturbance.

                                          Male-Mediated Developmental Toxicity

                                          While developmental toxicity is usually considered to result from exposure of the female and the conceptus—that is, teratogenic effects—there is increasing evidence from both animal and human studies for male-mediated developmental effects. Proposed mechanisms for such effects include transmission of chemicals from the father to the conceptus via seminal fluid, indirect contamination of the mother and the conceptus by substances carried from the workplace into the home environment through personal contamination, and—as noted earlier—paternal preconception exposures that result in transmissible genetic changes (mutations).

                                           

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                                          Thursday, 17 February 2011 23:36

                                          Occupational Neuroepidemiology

                                          Olav Axelson*

                                          *Adapted from Axelson 1996.

                                          Early knowledge about the neurotoxic effects of occupational exposures appeared through clinical observations. The observed effects were more or less acute and concerned exposure to metals such as lead and mercury or solvents like carbon disulphide and trichloroethylene. With time, however, more chronic and clinically less obvious effects of neurotoxic agents have been assessed through modern examination methods and systematic studies of larger groups. Still, the interpretation of the findings has been controversial and debated such as the chronic effects of solvent exposure (Arlien-Søborg 1992).

                                          The difficulties met in interpreting chronic neurotoxic effects depend on both the diversity and vagueness of symptoms and signs and the associated problem of defining a proper disease entity for conclusive epidemiological studies. For example, in solvent exposure, the chronic effects might include memory and concentration problems, tiredness, lack of initiative, affect liability, irritability, and sometimes dizziness, headache, alcohol intolerance, and reduced libido. Neurophysiological methods have also revealed various functional disturbances, again difficult to condense into any single disease entity.

                                          Similarly, a variety of neurobehavioural effects also seems to occur due to other occupational exposures, such as moderate lead exposure or welding with some exposure to aluminium, lead, and manganese or exposure to pesticides. Again there are also neurophysiological or neurological signs, among others, polyneuropathy, tremor, and disturbance of equilibrium, in individuals exposed to organochlorine, organophosphorus and other insecticides.

                                          In view of the epidemiological problems involved in defining a disease entity out of the many types of neurobehavioural effects referred to, it has also become natural to consider some clinically, more or less well-defined neuropsychiatric disorders in relation to occupational exposures.

                                          Since the 1970s several studies have especially focused on solvent exposure and the psycho-organic syndrome, when of disabling severity. More recently also Alzheimer’s dementia, multiple sclerosis, Parkinson’s disease, amyotrophic lateral sclerosis, and related conditions have attracted interest in occupational epidemiology.

                                          Regarding solvent exposure and the psycho-organic syndrome (or toxic chronic encephalopathy in clinical occupational medicine, when exposure is taken into diagnostic account), the problem of defining a proper disease entity was apparent and first led to considering en bloc the diagnoses of encephalopathia, dementia, and cerebral atrophy, but neurosis, neurasthenia, and nervositas were also included as not necessarily distinct from each other in medical practice (Axelson, Hane and Hogstedt 1976). Recently, more specific disease entities, such as organic dementia and cerebral atrophy, have also been associated with solvent exposure (Cherry, Labréche and McDonald 1992). The findings have not been totally consistent, however, as no excess of “presenile dementia” appeared in a large-scale case-referent study in the United States with as many as 3,565 cases of various neuropsychiatric disorders and 83,245 hospital referents (Brackbill, Maizlish and Fischbach 1990). However, in comparison with bricklayers, there was about a 45% excess of disabling neuropsychiatric disorders among white male painters, except spray painters.

                                          Occupational exposures also seem to play a role for disorders more specific than the psycho-organic syndrome. Hence, in 1982, an association between multiple sclerosis and solvent exposure from glues was first indicated in the Italian shoe industry (Amaducci et al. 1982). This relationship has been considerably strengthened by further studies in Scandinavia (Flodin et al. 1988; Landtblom et al. 1993; Grönning et al. 1993) and elsewhere, so that 13 studies with some information on solvent exposure could be considered in a review (Landtblom et al. 1996). Ten of these studies provided enough data for inclusion in a meta-analysis, showing about a twofold risk for multiple sclerosis among individuals with solvent exposure. Some studies also associate multiple sclerosis with radiological work, welding, and work with phenoxy herbicides (Flodin et al. 1988; Landtblom et al. 1993). Parkinson’s disease seems to be more common in rural areas (Goldsmith et al. 1990), especially at younger ages (Tanner 1989). More interestingly, a study from Calgary, Canada, showed a threefold risk for herbicide exposure (Semchuk, Love and Lee 1992).

                                          All the case persons who recalled specific exposures reported exposure to phenoxy herbicides or thiocarbamates. One of them recalled exposure to paraquat, which is chemically similar to MPTP (N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine), an inducer of a Parkinson-like syndrome. Paraquat workers have not yet been found to suffer from such a syndrome, however (Howard 1979). Case-referent studies from Canada, China, Spain, and Sweden have indicated a relation with exposure to unspecified industrial chemicals, pesticides, and metals, especially manganese, iron and aluminium (Zayed et al. 1990).

                                          In a study from the United States, an increased risk of motor neuron disease (encompassing amyotrophic lateral sclerosis, progressive bulbar palsy and progressive muscular atrophy) appeared in connection with welding and soldering (Armon et al. 1991). Welding also appeared as a risk factor, as did electricity work, and also work with impregnating agents in a Swedish study (Gunnarsson et al. 1992). Hereditability for neurodegenerative and thyroid disease, combined with solvent exposure and male gender, showed a risk as high as 15.6. Other studies also indicate that exposure to lead and solvents could be of importance (Campbell, Williams and Barltrop 1970; Hawkes, Cavanagh and Fox 1989; Chio, Tribolo and Schiffer 1989; Sienko et al. 1990).

                                          For Alzheimer’s disease, no clear indication of any occupational risk appeared in a meta-analysis of eleven case-referent studies (Graves et al. 1991), but more recently an increased risk was connected with blue-collar work (Fratiglioni et al. 1993). Another new study, which included also the oldest ages, indicated that solvent exposure could be a rather strong risk factor (Kukull et al. 1995). The recent suggestion that Alzheimer’s disease might be related to exposure to electromagnetic fields was perhaps even more surprising (Sobel et al. 1995). Both these studies are likely to stimulate interest in several new investigations along the indicated lines.

                                          Hence, in view of the current perspectives in occupational neuroepidemiology, as briefly outlined, there seems to be a reason for conducting additional work-related studies of different, hitherto more or less neglected, neurological and neuropsychiatric disorders. It is not unlikely that there are some contributing effects from various occupational exposures, in the same manner as we have seen for many cancer types. In addition, as in etiologic cancer research, new clues suggesting ultimate causes or triggering mechanisms behind some of the serious neurological disorders may be obtained from occupational epidemiology.

                                           

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                                          Thursday, 17 February 2011 23:33

                                          Diagnosis

                                          The diagnosis of neurotoxic disease is not easy. The errors are usually of two types: either it is not recognized that a neurotoxic agent is the cause of neurological symptoms, or neurological (and especially neurobehavioural) symptoms are erroneously diagnosed as resulting from an occupational, neurotoxic exposure. Both of these errors can be hazardous since an early diagnosis is important in the case of neurotoxic disease, and the best treatment is avoiding further exposure for the individual case and the surveillance of the condition of other workers in order to prevent their exposure to the same danger. On the other hand, sometimes undue alarm can develop in the workplace if a worker claims to have serious symptoms and suspects a chemical exposure as the cause but in fact, either the worker is mistaken or the hazard is not actually present for others. There is practical reason for correct diagnostic procedures, as well, since in many countries, the diagnosis and treatment of occupational diseases and the loss of working capacity and invalidity caused by those diseases are covered by insurance; thus the financial compensation may be disputed, if the diagnostic criteria are not solid. An example of a decision tree for neurological assessment is given in Table 1.


                                          Table 1. Decision tree for neurotoxic disease

                                          I. Relevant exposure level, length and type

                                          II. Appropriate symptoms insidiously increasing central (CNS) or peripheral (PNS) nervous system symptoms

                                          III. Signs and additional tests CNS dysfunction: neurology, psychology tests PNS dysfunction: quantitative sensory test, nerve conduction studies

                                          IV. Other diseases excluded in differential diagnosis


                                          Exposure and Symptoms

                                          Acute neurotoxic syndromes occur mainly in accidental situations, when workers are exposed short-term to very high levels of a chemical or to a mixture of chemicals generally through inhalation. The usual symptoms are vertigo, malaise and possible loss of consciousness as a result of depression of the central nervous system. When the subject is removed from the exposure, the symptoms disappear rather quickly, unless the exposure has been so intense that it is life-threatening, in which case coma and death may follow. In these situations recognition of the hazard must occur at the workplace, and the victim should be taken out into the fresh air immediately.

                                          In general, neurotoxic symptoms arise after short-term or long-term exposures, and often at relatively low-level occupational exposure levels. In these cases acute symptoms may have occurred at work, but the presence of acute symptoms is not necessary for diagnosis of chronic toxic encephalopathy or toxic neuropathy to be made. However, patients do often report headache, light-headedness or mucosal irritation at the end of a working day, but these symptoms initially disappear during the night, weekend or vacation. A useful checklist can be found in Table 2.

                                          Table 2. Consistent neuro-functional effects of worksite exposures to some leading neurotoxic substances

                                           

                                          Mixed organic solvents

                                          Carbon disulphide

                                          Styrene

                                          Organophos-
                                          phates

                                          Lead

                                          Mercury

                                          Acquisition

                                          +




                                          +


                                          Affect

                                          +


                                          +


                                          +


                                          Categorization

                                          +






                                          Coding

                                          +

                                          +



                                          +

                                          +

                                          Colour vision

                                          +


                                          +




                                          Concept shifting

                                          +






                                          Distractibility





                                          +


                                          Intelligence

                                          +

                                          +


                                          +

                                          +

                                          +

                                          Memory

                                          +

                                          +

                                          +

                                          +

                                          +

                                          +

                                          Motor coordination

                                          +

                                          +

                                          +


                                          +

                                          +

                                          Motor speed

                                          +

                                          +

                                          +


                                          +

                                          +

                                          Near visual contrast sensitivity

                                          +






                                          Odour perception threshold

                                          +






                                          Odour identification

                                          +




                                          +


                                          Personality

                                          +

                                          +




                                          +

                                          Spatial relations

                                          +

                                          +



                                          +


                                          Vibrotactile threshold

                                          +



                                          +


                                          +

                                          Vigilance

                                          +

                                          +



                                          +


                                          Visual field





                                          +

                                          +

                                          Vocabulary





                                          +


                                          Source: Adapted from Anger 1990.

                                          Assuming that the patient has been exposed to neurotoxic chemicals, the diagnosis of neurotoxic disease starts with symptoms. In 1985, a joint working group of the World Health Organization and the Nordic Council of Ministers discussed the matter of chronic organic solvent intoxication and found a set of core symptoms, which are found in most cases (WHO/Nordic Council 1985). The core symptoms are fatigability, memory loss, difficulties in concentration, and loss of initiative. These symptoms usually start after a basic change in personality, which develops gradually and affects energy, intellect, emotion and motivation. Among other symptoms of chronic toxic encephalopathy are depression, dysphoria, emotional lability, headache, irritability, sleep disturbances and dizziness (vertigo). If there is also involvement of the peripheral nervous system, numbness and possibly muscular weakness develop. Such chronic symptoms last for at least a year after the exposure itself has ended.

                                          Clinical Examination and Testing

                                          The clinical examination should include a neurological examination, where attention should be paid to impairment of higher nervous functions, such as memory, cognition, reasoning and emotion; to impaired cerebellar functions, like tremor, gait, station and coordination; and to peripheral nervous functions, especially vibration sensitivity and other tests of sensation. Psychological tests can provide objective measures of higher nervous system functions, including psychomotor, short-term memory, verbal and non-verbal reasoning and perceptual functions. In individual diagnosis the tests should include some tests that give a clue as to the person’s premorbid intellectual level. History of school performance and previous job performance as well as possible psychological tests administered previously, for example in connection with military service, can help in the evaluation of the person’s normal level of performance.

                                          The peripheral nervous system can be studied with quantitative tests of sensory modalities, vibration and thermosensibility. Nerve conduction velocity studies and electromyography can often reveal neuropathy at an early stage. In these tests special emphasis should be on sensory nerve functions. The amplitude of the sensory action potential (SNAP) decreases more often than the sensory conduction velocity in axonal neuropathies, and most toxic neuropathies are axonal in character. Neuroradiological studies such as computed tomography (CT) and magnetic resonance imaging (MRI) usually do not reveal anything pertinent to chronic toxic encephalopathy, but they may be useful in the differential diagnosis.

                                          In the differential diagnosis other neurological and psychiatric diseases should be considered. Dementia of other aetiology should be ruled out, as well as depression and stress symptoms of various causes. Psychiatric consultation may be necessary. Alcohol abuse is a relevant confounding factor; excessive use of alcohol causes symptoms similar to those of solvent exposure, and on the other hand there are papers indicating that solvent exposure may induce alcohol abuse. Other causes for neuropathy also have to be ruled out, especially entrapment neuropathies, diabetes and kidney disease; also alcohol causes neuropathy. The combination of encephalopathy and neuropathy is more likely of toxic origin than either of these alone.

                                          In the final decision the exposure should be evaluated again. Was there relevant exposure, considering the level, length and quality of exposure? Solvents are more likely to induce psycho-organic syndrome or toxic encephalopathy; hexacarbons, however, usually first cause neuropathy. Lead and some other metals cause neuropathy, although CNS involvement can be detected later on.

                                           

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                                          Thursday, 17 February 2011 23:31

                                          Measuring Neurotoxic Deficits

                                          Neuro-functional Test Batteries

                                          Sub-clinical neurologic signs and symptoms have long been noted among active workers exposed to neurotoxins; however, it is only since the mid-1960s that research efforts have focused on the development of sensitive test batteries capable of detecting subtle, mild changes that are present in the early stages of intoxication, in perceptual, psychomotor, cognitive, sensory and motor functions, and affect.

                                          The first neurobehavioural test battery for use in worksite studies was developed by Helena Hänninen, a pioneer in the field of neurobehavioural deficits associated with toxic exposure (Hänninen Test Battery) (Hänninen and Lindstrom 1979). Since then, there have been worldwide efforts to develop, refine and, in some cases, computerize neurobehavioural test batteries. Anger (1990) describes five worksite neurobehavioural test batteries from Australia, Sweden, Britain, Finland and the United States, as well as two neurotoxic screening batteries from the United States, that have been used in studies of neurotoxin-exposed workers. In addition, the computerized Neurobehavioral Evaluation System (NES) and the Swedish Performance Evaluation System (SPES) have been extensively used around the world. There are also test batteries designed to assess sensory functions, including measures of vision, vibrotactile perception threshold, smell, hearing and sway (Mergler 1995). Studies of various neurotoxic agents using one or another of these batteries have greatly contributed to our knowledge of early neurotoxic impairment; however, cross-study comparisons have been difficult since different tests are used and tests with similar names may be administered using a different protocol.

                                          In an attempt to standardize information from studies on neurotoxic substances, the notion of a “core” battery was put forward by a working committee of the World Health Organization (WHO) (Johnson 1987). Based on knowledge at the time of the meeting (1985), a series of tests were selected to make up the Neurobehavioral Core Test Battery (NCTB), a relatively inexpensive, hand-administered battery, which has been successfully used in many countries (Anger et al. 1993). The tests that make up this battery were chosen to cover specific nervous system domains, which had been previously shown to be sensitive to neurotoxic damage. A more recent core battery, which comprises both hand-administered and computerized tests, has been proposed by a workgroup of the United States Agency for Toxic Substances and Disease Registry (Hutchison et al. 1992). Both batteries are presented in Table 1.

                                          Table 1. Examples of "core" batteries for assessment of early neurotoxic effects

                                          Neurobehavioural Core Test Battery (NCTB)+

                                          Test order

                                          Agency for Toxic Substances and Disease Registry Adult Environmental Neurobehavioural Test Battery (AENTB)+

                                          Functional domain

                                          Test

                                           

                                          Functional domain

                                          Test

                                          Motor steadiness

                                          Aiming (Pursuit Aiming II)

                                          1

                                          Vision

                                          Visual acuity, near contrast sensitivity

                                          Attention/response speed

                                          Simple Reaction Time

                                          2

                                           

                                          Colour vision (Lanthony D-15 desaturated test)

                                          Perceptual motor speed

                                          Digit Symbol (WAIS-R)

                                          3

                                          Somatosensory

                                          Vibrotactile perception threshold

                                          Manual dexterity

                                          Santa Ana (Helsinki Version)

                                          4

                                          Motor strength

                                          Dynamometer (including fatigue assessment)

                                          Visual perception/memory

                                          Benton Visual Retention

                                          5

                                          Motor coordination

                                          Santa Ana

                                          Auditory memory

                                          Digit Span (WAIS-R, WMS)

                                          6

                                          Higher intellectual function

                                          Raven Progressive Matrices (Revised)

                                          Affect

                                          POMS (Profile of Mood States)

                                          7

                                          Motor coordination

                                          Fingertapping Test (one hand)1

                                             

                                          8

                                          Sustained attention (cognitive), speed (motor)

                                          Simple Reaction Time (SRT) (extended)1

                                             

                                          9

                                          Cognitive coding

                                          Symbol-digit with delayed recall1

                                             

                                          10

                                          Learning and memory

                                          Serial Digit Learning1

                                             

                                          11

                                          Index of educational level

                                          Vocabulary1

                                             

                                          12

                                          Mood

                                          Mood Scale1

                                          1 Available in computerized version; WAIS = Wechsler Adult Intelligence Scale; WMS = Wechsler Memory Scale.

                                           

                                          The authors of both core batteries stress that, although the batteries are useful to standardize results, they by no means provide complete assessment of nervous system functions. Additional tests should be used depending upon the type of exposure; for example, a test battery to assess nervous system dysfunction among manganese-exposed workers would include more tests of motor functions, particularly those that require rapid alternating movements, while one for methylmercury-exposed workers would include visual field testing. The choice of tests for any particular workplace should be made on the basis of current knowledge on the action of the particular toxin or toxins to which the persons are exposed.

                                          More sophisticated test batteries, administered and interpreted by trained psychologists, are an important part of the clinical assessment for neurotoxic poisoning (Hart 1988). It includes tests of intellectual ability, attention, concentration and orientation, memory, visuo-perceptive, constructive and motor skills, language, conceptual and executive functions, and psychological well-being, as well as an assessment of possible malingering. The profile of the patient’s performance is examined in the light of past and present medical and psychological history, as well as exposure history. The final diagnosis is based on a constellation of deficits interpreted in relation to the type of exposure.

                                          Measures of Emotional State and Personality

                                          Studies of the effects of neurotoxic substances usually include measures of affective or personality disturbance, in the form of symptoms questionnaires, mood scales or personality indices. The NCTB, described above, includes the Profile of Mood States (POMS), a quantitative measure of mood. Using 65 qualifying adjectives of mood states over the past 8 days, the degrees of tension, depression, hostility, vigour, fatigue and confusion are derived. Most comparative workplace studies of neurotoxic exposure indicate differences between exposed and non-exposed. A recent study of styrene-exposed workers shows dose-response relations between post-shift urinary mandelic acid level, a biological indicator of styrene, and scale scores of tension, hostility, fatigue and confusion (Sassine et al. 1996).

                                          Lengthier and more sophisticated tests of affect and personality, such as the Minnesota Multiphasic Personality Index (MMPI), which reflect both emotional states and personality traits, have been used primarily for clinical evaluation, but also in workplace studies. The MMPI likewise provides an assessment of symptom exaggeration and inconsistent responses. In a study of microelectronics workers with a history of exposure to neurotoxic substances, results from the MMPI indicated clinically significant levels of depression, anxiety, somatic concerns and disturbances of thinking (Bowler et al. 1991).

                                          Electrophysiological Measures

                                          Electrical activity generated by the transmission of information along nerve fibres and from one cell to another, can be recorded and used in the determination of what is happening in the nervous system of persons with toxic exposures. Interference with neuronal activity can slow down transmission or modify the electrical pattern. Electrophysiological recordings require precise instruments and are most frequently carried out in a laboratory or hospital setting. There have, however, been efforts to develop more portable equipment for use in workplace studies.

                                          Electrophysiological measures record a global response of a large number of nerve fibres and/or fibres, and a fair amount of damage must exist before it can be adequately recorded. Thus, for most neurotoxic substances, symptoms, as well as sensory, motor and cognitive changes, usually can be detected in groups of exposed workers before electrophysiological differences are observed. For clinical examination of persons with suspected neurotoxic disorders, electrophysiological methods provide information concerning the type and extent of nervous system damage. A review of electrophysiological techniques used in the detection of early neurotoxicity in humans is provided by Seppalaïnen (1988).

                                          The nerve conduction velocity of sensory nerves (going towards the brain) and motor nerves (going away from the brain) are measured by electroneurography (ENG). By stimulating at different anatomical positions and recording at another, the conduction velocity can be calculated. This technique can provide information about the large myelinated fibres; slowing of conduction velocity occurs when demyelination is present. Reduced conduction velocities have frequently been observed among lead-exposed workers, in the absence of neurological symptoms (Maizlish and Feo 1994). Slow conduction velocities of peripheral nerves have also been associated with other neurotoxins, such as mercury, hexacarbons, carbon disulphide, styrene, methyl-n-butyl ketone, methyl ethyl ketone, and certain solvent mixtures. The trigeminal nerve (a facial nerve) is affected by trichloroethylene exposure. However, if the toxic substance acts primarily on thinly myelinated or unmyelinated fibres, conduction velocities usually remain normal.

                                          Electromyography (EMG) is used for measuring the electrical activity in muscles. Electromyographic abnormalities have been observed among workers with exposure to such substances as n-hexane, carbon disulphide, methyl-n-butyl ketone, mercury and certain pesticides. These changes are often accompanied by changes in ENG and symptoms of peripheral neuropathy.

                                          Changes in brainwaves are evidenced by electroencephalography (EEG). In patients with organic solvent poisoning, local and diffuse slow wave abnormalities have been observed. Some studies report evidence of dose-related EEG alterations among active workers, with exposure to organic solvent mixtures, styrene and carbon disulphide. Organochlorine pesticides can cause epileptic seizures, with EEG abnormalities. EEG changes have been reported with long-term exposure to organophosphorus and zinc phosphide pesticides.

                                          Evoked potentials (EP) provides another means of examining nervous system activity in response to a sensory stimulus. Recording electrodes are placed on the specific area of the brain that responds to the particular stimuli, and the latency and amplitude of the event-related slow potential are recorded. Increased latency and/or reduced peak amplitudes have been observed in response to visual, auditory and somatosensory stimuli for a wide range of neurotoxic substances.

                                          Electrocardiography (ECG or EKG) records changes in the electrical conduction of the heart. Although it is not often used in studies of neurotoxic substances, changes in ECG waves have been observed among persons with exposure to trichloroethylene. Electro-oculographic (EOG) recordings of eye movements have shown alterations among workers with exposure to lead.

                                          Brain Imaging Techniques

                                          In recent years, different techniques have been developed for brain imaging. Computed tomographic (CT) images reveal the anatomy of the brain and spinal cord. They have been used to study cerebral atrophy among solvent-exposed workers and patients; however, the results are not consistent. Magnetic resonance imaging (MRI) examines the nervous system using a powerful magnetic field. It is particularly useful clinically to rule out an alternative diagnosis, such as brain tumours. Positron Emission Tomography (PET), which yields images of biochemical processes, has been successfully used to study changes in the brain induced by manganese intoxication. Single photon emission computed tomography (SPECT) provides information about brain metabolism and may prove to be an important tool in understanding how neurotoxins act on the brain. These techniques are all very costly, and not readily available in most hospitals or laboratories throughout the world.

                                           

                                          Back

                                          Neurotoxicant syndromes, brought about by substances which adversely affect nervous tissue, constitute one of the ten leading occupational disorders in the United States. Neurotoxicant effects constitute the basis for establishing exposure limit criteria for approximately 40% of agents considered hazardous by the United States National Institute for Occupational Safety and Health (NIOSH).

                                          A neurotoxin is any substance capable of interfering with the normal function of nervous tissue, causing irreversible cellular damage and/or resulting in cellular death. Depending on its particular properties, a given neurotoxin will attack selected sites or specific cellular elements of the nervous system. Those compounds, which are non-polar, have greater lipid solubility, and thus have greater access to nervous tissue than highly polar and less lipid-soluble chemicals. The type and size of cells and the various neurotransmitter systems affected in different regions of the brain, innate protective detoxifying mechanisms, as well as the integrity of cellular membranes and intracellular organelles all influence neurotoxicant responses.

                                          Neurons (the functional cell unit of the nervous system) have a high metabolic rate and are at greatest risk for neurotoxicant damage, followed by oligodendrocytes, astrocytes, microglia and cells of the capillary endothelium. Changes in cellular membrane structure impair excitability and impede impulse transmission. Toxicant effects alter protein form, fluid content and ionic exchange capability of membranes, leading to swelling of neurons, astrocytes and damage to the delicate cells lining blood capillaries. Disruption of neurotransmitter mechanisms block access to post-synaptic receptors, produce false neurotransmitter effects, and alter the synthesis, storage, release, re-uptake or enzymatic inactivation of natural neurotransmitters. Thus, clinical manifestations of neurotoxicity are determined by a number of different factors: the physical characteristics of the neurotoxicant substance, the dose of exposure to it, the vulnerability of the cellular target, the organism’s ability to metabolize and excrete the toxin, and by the reparative abilities of the structures and mechanisms affected. Table 1 lists various chemical exposures and their neurotoxic syndromes.

                                          Table 1. Chemical exposures and associated neurotoxic syndromes

                                          Neurotoxin

                                          Sources of exposure

                                          Clinical diagnosis

                                          Locus of pathology1

                                          Metals

                                          Arsenic

                                          Pesticides; pigments; antifouling paint; electroplating industry; seafood; smelters; semiconductors

                                          Acute: encephalopathy

                                          Chronic: peripheral neuropathy

                                          Unknown (a)

                                          Axon (c)

                                          Lead

                                          Solder; lead shot; illicit whiskey; insecticides; auto body shop; storage battery manufacturing; foundries, smelters; lead-based paint; lead pipes

                                          Acute: encephalopathy

                                          Chronic: encephalopathy and peripheral neuropathy

                                          Blood vessels (a)

                                          Axon (c)

                                          Manganese

                                          Iron, steel industry; welding operations; metal-finishing operations; fertilizers; manufacturers of fireworks, matches; manufacturers of dry cell batteries

                                          Acute: encephalopathy

                                          Chronic: parkinsonism

                                          Unknown (a)

                                          Basal ganglia neurons (c)

                                          Mercury

                                          Scientific instruments; electrical equipment; amalgams; electroplating industry; photography; felt making

                                          Acute: headache, nausea, onset of tremor

                                          Chronic: ataxia, peripheral neuropathy, encephalopathy

                                          Unknown (a)

                                          Axon (c)

                                          Unknown (c)

                                          Tin

                                          Canning industry; solder; electronic components; polyvinyl plastics; fungicides

                                          Acute: memory defects, seizures, disorientation

                                          Chronic: encephalomyelopathy

                                          Neurons of the limbic system (a & c)

                                          Myelin (c)

                                          Solvents

                                          Carbon disulphide

                                          Manufacturers of viscose rayon; preservatives; textiles; rubber cement; varnishes; electroplating industry

                                          Acute: encephalopathy

                                          Chronic: peripheral neuropathy, parkinsonism

                                          Unknown (a)

                                          Axon (c)

                                          Unknown

                                          n-hexane,

                                          methyl butyl ketone

                                          Paints; lacquers; varnishes; metal-cleaning compounds; quick-drying inks; paint removers; glues, adhesives

                                          Acute: narcosis

                                          Chronic: peripheral neuropathy, unknown (a) Axon (c),

                                           

                                          Perchloroethylene

                                          Paint removers; degreasers; extraction agents; dry cleaning industry; textile industry

                                          Acute: narcosis

                                          Chronic: peripheral neuropathy, encephalopathy

                                          Unknown (a)

                                          Axon (c)

                                          Unknown

                                          Toluene

                                          Rubber solvents; cleaning agents; glues; manufacturers of benzene; gasoline, aviation fuels; paints, paint thinners; lacquers

                                          Acute: narcosis

                                          Chronic: ataxia, encephalopathy

                                          Unknown (a)

                                          Cerebellum (c)

                                          Unknown

                                          Trichloroethylene

                                          Degreasers; painting industry; varnishes; spot removers; process of decaffeination; dry cleaning industry; rubber solvents

                                          Acute: narcosis

                                          Chronic: encephalopathy, cranial neuropathy

                                          Unknown (a)

                                          Unknown (c)

                                          Axon (c)

                                           Insecticides

                                           Organophosphates

                                           Agricultural industry manufacturing and application

                                           Acute: cholinergic poisoning

                                           Chronic: ataxia, paralysis, peripheral neuropathy

                                           Acetylcholinesterase (a)

                                           Long tracts of spinal cord (c)

                                           Axon (c)

                                           Carbamates

                                           Agricultural industry manufacturing and application flea powders

                                           Acute: cholinergic poisoning Chronic: tremor, peripheral neuropathy

                                           Acetylcholinesterase (a)

                                           Dopaminergic system (c)

                                           1 (a), acute; (c), chronic.

                                          Source: Modified from Feldman 1990, with permission of the publisher.

                                           

                                          Establishing a diagnosis of a neurotoxicant syndrome and differentiating it from neurologic diseases of non-neurotoxicant aetiology requires an understanding of the pathogenesis of the neurological symptoms and observed signs and symptoms; an awareness that particular substances are capable of affecting nervous tissue; documentation of exposure; evidence of presence of neurotoxin and/or metabolites in tissues of an affected individual; and careful delineation of a time relationship between exposure and the appearance of symptoms with subsequent decrease in symptoms after exposure is ended.

                                          Proof that a particular substance has reached a toxicant dose level is usually lacking after symptoms appear. Unless environmental monitoring is ongoing, a high index of suspicion is necessary to recognize cases of neurotoxicologic injury. Identifying symptoms referable to the central and/or the peripheral nervous systems can help the clinician focus on certain substances, which have a greater predilection for one part or another of the nervous system, as possible culprits. Convulsions, weakness, tremor/twitching, anorexia (weight loss), equilibrium disturbance, central nervous system depression, narcosis (a state of stupor or unconsciousness), visual disturbance, sleep disturbance, ataxia (inability to coordinate voluntary muscle movements), fatigue and tactile disorders are commonly reported symptoms following exposure to certain chemicals. Constellations of symptoms form syndromes associated with neurotoxicant exposure.

                                          Behavioural Syndromes

                                          Disorders with predominantly behavioural features ranging from acute psychosis, depression and chronic apathy have been described in some workers. It is essential to differentiate memory impairment associated with other neurological diseases, such as Alzheimer’s disease, arteriosclerosis or presence of a brain tumour, from the cognitive deficits associated with toxicant exposure to organic solvents, metals or insecticides. Transient disturbances of awareness or epileptic seizures with or without associated motor involvement must be identified as a primary diagnosis separate from similarly appearing disturbances of consciousness related to neurotoxicant effects. Subjective and behavioural toxicant syndromes such as headache, vertigo, fatigue and personality change manifest as mild encephalopathy with inebriation, and may indicate the presence of exposure to carbon monoxide, carbon dioxide, lead, zinc, nitrates or mixed organic solvents. Standardized neuropsychological testing is necessary to document elements of cognitive impairment in patients suspected of toxicant encephalopathy, and these must be differentiated from those dementing syndromes caused by other pathologies. Specific tests used in the diagnostic batteries of tests must include a broad sampling of cognitive function tests which will generate predictions about the patient’s functioning and daily life, as well as tests which have been demonstrated previously to be sensitive to the effects of known neurotoxins. These standardized batteries must include tests which have been validated on patients with specific types of brain damage and structural deficits, to clearly separate these conditions from neurotoxic effects. In addition, tests must include internal control measures to detect the influence of motivation, hypochondriasis, depression and learning difficulties, and must contain language that takes into account cultural as well as educational background effects.

                                          A continuum exists from mild to severe central nervous system impairment experienced by patients exposed to toxicant substances:

                                            • Organic affective syndrome (Type I Effect), in which mild mood disorders predominate as the patient’s chief complaint, with features most consistent with those of organic affective disorders of the depressive type. This syndrome seems to be reversible following cessation of exposure to the offending agent.
                                            • Mild chronic toxicant encephalopathy, in which, in addition to mood disturbances, central nervous system impairment is more prominent. Patients have evidence of memory and psychomotor function disturbance which can be confirmed by neuropsychological testing. In addition, features of visual spatial impairment and abstract concept formation may be seen. Activities of daily living and work performance are impaired.
                                            • Sustained personality or mood change (Type IIA Effect) or impairment in intellectual function (Type II) may be seen. In mild chronic toxicant encephalopathy, the course is insidious. Features may persist after the cessation of exposure and disappear gradually, while in some individuals, persistent functional impairment may be observed. If exposure continues, the encephalopathy may progress to a more severe stage.
                                            • In severe chronic toxicant encephalopathy (Type III Effect) dementia with global deterioration of memory and other cognitive problems are noted. The clinical effects of toxicant encephalopathy are not specific to a given agent. Chronic encephalopathy associated with toluene, lead and arsenic is not different from that of other toxicant aetiologies. The presence of other associated findings, however (visual disturbances with methyl alcohol), may help differentiate syndromes according to particular chemical aetiologies.

                                                   

                                                  Workers exposed to solvents for long periods of time may exhibit disturbances of central nervous system function which are permanent. Since an excess of subjective symptoms, including headache, fatigue, impaired memory, loss of appetite and diffuse chest pains, have been reported, it is often difficult to confirm this effect in any individual case. An epidemiological study comparing house painters exposed to solvents with unexposed industrial workers showed, for example, that painters had significantly lower mean scores on psychological tests measuring intellectual capacity and psychomotor coordination than referent subjects. The painters also had significantly lower performances than expected on memory and reaction time tests. Differences between workers exposed for several years to jet fuel and unexposed workers, in tests demanding close attention and high sensory motor speed, were apparent as well. Impairments in psychological performance and personality changes have also been reported among car painters. These included visual and verbal memory, reduction of emotional reactivity, and poor performance on verbal intelligence tests.

                                                  Most recently, a controversial neurotoxicant syndrome, multiple chemical sensitivity, has been described. Such patients develop a variety of features involving multiple organ systems when they are exposed to even low levels of various chemicals found in the workplace and the environment. Mood disturbances are characterized by depression, fatigue, irritability and poor concentration. These symptoms reoccur on exposure to predictable stimuli, by elicitation by chemicals of diverse structural and toxicological classes, and at levels much lower than those causing adverse responses in the general population. Many of the symptoms of multiple chemical sensitivity are shared by individuals who show only a mild form of mood disturbance, headache, fatigue, irritability and forgetfulness when they are in a building with poor ventilation and with off-gassing of volatile substances from synthetic building materials and carpets. The symptoms disappear when they leave these environments.

                                                  Disturbances of consciousness, seizures and coma

                                                  When the brain is deprived of oxygen—for example, in the presence of carbon monoxide, carbon dioxide, methane or agents which block tissue respiration such as hydrocyanic acid, or those which cause massive impregnation of the nerve such as certain organic solvents—disturbances of consciousness may result. Loss of consciousness may be preceded by seizures in workers with exposure to anticholinesterase substances such as organophosphate insecticides. Seizures may also occur with lead encephalopathy associated with brain swelling. Manifestations of acute toxicity following organophosphate poisoning have autonomic nervous system manifestations which precede the occurrence of dizziness, headache, blurred vision, myosis, chest pain, increased bronchial secretions, and seizures. These parasympathetic effects are explained by the inhibitory action of these toxicant substances on cholinesterase activity.

                                                  Movement disorders

                                                  Slowness of movement, increased muscle tone, and postural abnormalities have been observed in workers exposed to manganese, carbon monoxide, carbon disulphide and the toxicity of a meperidine by-product, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). At times, the individuals may appear to have Parkinson’s disease. Parkinsonism secondary to toxicant exposure has features of other nervous disorders such as chorea and athetosis. The typical “pill-rolling” tremor is not seen in these instances, and usually the cases do not respond well to the drug levodopa. Dyskinesia (impairment of the power of voluntary motion) can be a common symptom of bromomethane poisoning. Spasmodic movements of the fingers, face, peribuccal muscles and the neck, as well as extremity spasms, may be seen. Tremor is common following mercury poisoning. More obvious tremor associated with ataxia (lack of coordination of muscular action) is noted in individuals following toluene inhalation.

                                                  Opsoclonus is an abnormal eye movement which is jerky in all directions. This is often seen in brain-stem encephalitis, but may also be a feature following chlordecone exposure. The abnormality consists of irregular bursts of abrupt, involuntary, rapid, simultaneous jerking of both eyes in a conjugate manner, possibly multidirectional in severely affected individuals.

                                                  Headache

                                                  Common complaints of head pain following exposure to various metal fumes such as zinc and other solvent vapours may result from vasodilation (widening of the blood vessels), as well as cerebral oedema (swelling). The experiencing of pain is common to these conditions, as well as carbon monoxide, hypoxia (low oxygen), or carbon dioxide conditions. “Sick building syndrome” is thought to cause headaches because of excess carbon dioxide present in a poorly ventilated area.

                                                  Peripheral neuropathy

                                                  Peripheral nerve fibres serving motor functions begin in motor neurons in the ventral horn of the spinal cord. The motor axons extend peripherally to the muscles they innervate. A sensory nerve fibre has its nerve cell body in the dorsal root ganglion or in the dorsal grey matter of the spinal cord. Having received information from the periphery detected at distal receptors, nerve impulses are conducted centrally to the nerve cell bodies where they connect with spinal cord pathways transmitting information to the brain stem and cerebral hemispheres. Some sensory fibres have immediate connections with motor fibres within the spinal cord, providing a basis for reflex activity and quick motor responses to noxious sensations. These sensory-motor relationships exist in all parts of the body; the cranial nerves are the peripheral nerve equivalents arising in brain stem, rather than spinal cord, neurons. Sensory and motor nerve fibres travel together in bundles and are referred to as the peripheral nerves.

                                                  Toxicant effects of peripheral nerve fibres may be divided into those which primarily affect axons (axonopathies), those which are involved in distal sensory-motor loss, and those which primarily affect myelin sheath and Schwann cells. Axonopathies are evident in early stages in the lower extremities where the axons are the longest and farthest from the nerve cell body. Random demyelination occurs in segments between nodes of Ranvier. If sufficient axonal damage occurs, secondary demyelination follows; as long as axons are preserved, regeneration of Schwann cells and remyelination can occur. A pattern seen commonly in toxicant neuropathies is distal axonopathy with secondary segmental demyelination. The loss of myelin reduces the speed of conducting nerve impulses. Thus, gradual onset of intermittent tingling and numbness progressing to lack of sensation and unpleasant sensations, muscle weakness, and atrophy results from damage to the motor and sensory fibres. Reduced or absent tendon reflexes and anatomically consistent patterns of sensory loss, involving the lower extremities more than upper, are features of peripheral neuropathy.

                                                  Motor weaknesses may be noted in distal extremities and progress to unsteady gait and inability to grasp objects. The distal portions of the extremities are involved to a greater extent, but severe cases may produce proximal muscle weakness or atrophy as well. Extensor muscle groups are involved before the flexors. Symptoms may sometimes progress for a few weeks even after removal from exposure. Deterioration of nerve function may persist for several weeks after removal from exposure.

                                                  Depending on the type and severity of neuropathy, an electrophysiological examination of the peripheral nerves is useful to document impaired function. Slowing of conduction velocity, reduced amplitudes of sensory or motor action potentials, or prolonged latencies can be observed. Slowing of motor or sensory conduction velocities is generally associated with demyelination of nerve fibres. Preservation of normal conduction velocity values in the presence of muscle atrophy suggests axonal neuropathy. Exceptions occur when there is progressive loss of motor and sensory nerve fibres in axonal neuropathy which affects the maximal conduction speed as a result of the dropping out of the larger diameter faster conducting nerve fibres. Regenerating fibres occur in early stages of recovery in axonopathies, in which conduction is slowed, especially in the distal segments. The electrophysiological study of patients with toxicant neuropathies should include measurements of motor and sensory conduction velocity in the upper and lower extremities. Special attention should be given to the primarily sensory conducting characteristics of the sural nerve in the leg. This is of great value when the sural nerve is then used for biopsy, providing anatomical correlation between the histology of teased nerve fibres and the conduction characteristics. A differential electrophysiological study of the conducting capabilities of proximal segments versus distal segments of a nerve is useful in identifying a distal toxicant axonopathy, or to localize a neuropathic block of conduction, probably due to demyelination.

                                                  Understanding the pathophysiology of a suspected neurotoxicant polyneuropathy has great value. For example, in patients with neuropathy caused by n-hexane and methylbutyl ketone, motor nerve conduction velocities are reduced, but in some cases, the values may fall within the normal range if only the fastest firing fibres are stimulated and used as the measured outcome. Since neurotoxicant hexacarbon solvents cause axonal degeneration, secondary changes arise in myelin and explain overall reduction in conduction velocity despite the value within the normal range produced by the preserved conducting fibres.

                                                  Electrophysiological techniques include special tests other than the direct conduction velocity, amplitude and latency studies. Somatosensory evoked potentials, auditory evoked potentials, and visual evoked potentials are ways of studying the characteristics of the sensory conducting systems, as well as specific cranial nerves. Afferent-efferent circuitry can be tested by using blink reflex tests involving the 5th cranial nerve to 7th cranial innervated muscle responses; H-reflexes involve segmental motor reflex pathways. Vibration stimulation selects out larger fibres from smaller fibre involvements. Well-controlled electronic techniques are available for measuring the threshold needed to elicit a response, and then to determine the speed of travel of that response, as well as the amplitude of the muscle contraction, or the amplitude and pattern of an evoked sensory action potential. All physiological results must be evaluated in light of the clinical picture and with an understanding of the underlying pathophysiological process.

                                                  Conclusion

                                                  The differentiation of a neurotoxicant syndrome from a primary neurological disease poses a formidable challenge to physicians in the occupational setting. Obtaining a good history, maintaining a high degree of suspicion and adequate follow-up of an individual, as well as groups of individuals, is necessary and rewarding. Early recognition of illness related to toxicant agents in their environment or to a particular occupational exposure is critical, since proper diagnosis can lead to early removal of an individual from the hazards of ongoing exposure to a toxicant substance, preventing possible irreversible neurological damage. Furthermore, recognition of the earliest affected cases in a particular setting may result in changes that will protect others who have not yet become affected.

                                                   

                                                  Back

                                                  Current knowledge of the short- and long-term manifestations of exposure to neurotoxic substances comes from experimental animal studies and human chamber studies, epidemiological studies of active and retired and/or diseased workers, clinical studies and reports, as well as large-scale disasters, such as those that occurred in Bhopal, following a leak of methyl isocyanate, and in Minamata, from methyl mercury poisoning.

                                                  Exposure to neurotoxic substances can produce immediate effects (acute) and/or long-term effects (chronic). In both cases, the effects can be reversible and disappear over time following reduction or cessation of exposure, or result in permanent, irreversible damage. The severity of acute and chronic nervous system impairment depends on exposure dose, which includes both the quantity and duration of exposure. Like alcohol and recreational drugs, many neurotoxic substances may initially be excitatory, producing a sensation of well-being or euphoria and/or speeding up motor functions; as the dose increases in quantity or in time, these same neurotoxins will depress the nervous system. Indeed, narcosis (a state of stupor or insensibility) is induced by a large number of neurotoxic substances, which are mind-altering and depress the central nervous system.

                                                  Acute Poisoning

                                                  Acute effects reflect the immediate response to the chemical substance. The severity of the symptoms and resulting disorders depends on the quantity that reaches the nervous system. With mild exposures, acute effects are mild and transient, disappearing when exposure ceases. Headache, tiredness, light-headedness, difficulty concentrating, feelings of drunkenness, euphoria, irritability, dizziness and slowed reflexes are the types of symptoms experienced during exposure to neurotoxic chemicals. Although these symptoms are reversible, when exposure is repeated day after day, the symptoms recur as well. Moreover, since the neurotoxic substance is not immediately eliminated from the body, symptoms can persist following work. Reported symptoms at a particular workstation are a good reflection of chemical interference with the nervous system and should be considered a warning signal for potential over-exposure; preventive measures to reduce exposure levels should be initiated.

                                                  If exposure is very high, as can occur with spills, leaks, explosions and other accidents, symptoms and signs of intoxication are debilitating (severe headaches, mental confusion, nausea, dizziness, incoordination, blurred vision, loss of consciousness); if exposure is high enough, effects can be long-lasting, possibly resulting in coma and death.

                                                  Acute pesticide-related disorders are a common occurrence among agricultural workers in food-producing countries, where large amounts of toxic substances are used as insecticides, fungicides, nematicides, and herbicides. Organophosphates, carbamates, organochlorines, pyrethrum, pyrethrin, paraquat and diquat are among the major categories of pesticides; however, there are thousands of pesticide formulations, containing hundreds of different active ingredients. Some pesticides, such as maneb, contain manganese, while others are dissolved in organic solvents. In addition to the symptoms mentioned above, acute organophosphate and carbamate poisoning may be accompanied by salivation, incontinence, convulsions, muscle twitching, diarrhoea, visual disturbances, as well as respiratory difficulties and a rapid heart rate; these result from an excess of the neurotransmitter acetylcholine, which occurs when these substances attack a chemical called cholinesterase. Blood cholinesterase decreases proportionally to the degree of acute organophosphate or carbamate intoxication.

                                                  With some substances, such as organophosphorus pesticides and carbon monoxide, high-level acute exposures can produce delayed deterioration of certain parts of the nervous system. For the former, numbness and tingling, weakness and disequilibrium can occur a few weeks after exposure, while for the latter, delayed neurologic deterioration can take place, with symptoms of mental confusion, ataxia, motor incoordination and paresis. Repeated acute episodes of high levels of carbon monoxide have been associated with later-life Parkinsonism. It is possible that high exposures to certain neurotoxic chemicals may be associated with an increased risk for neurodegenerative disorders later on in life.

                                                  Chronic Poisoning

                                                  Recognition of the hazards of neurotoxic chemicals has led many countries to reduce the permissible exposure levels. However, for most chemicals, the level at which no adverse effect will occur over long-term exposure is still unknown. Repeated exposure to low to medium levels of neurotoxic substances throughout many months or years can alter nervous system functions in an insidious and progressive manner. Continued interference with molecular and cellular processes causes neurophysiological and psychological functions to undergo slow alterations, which in the early stages may go unseen since there are large reserves in the nervous system circuitry and damage can, in the first stages, be compensated through new learning.

                                                  Thus, initial nervous system injury is not necessarily accompanied by functional disorders and may be reversible. However, as the damage progresses, symptoms and signs, often non-specific in nature, become apparent, and individuals may seek medical attention. Finally, impairment may become so severe that a clear clinical syndrome, generally irreversible, is manifest.

                                                  Figure 1 schematizes the health deterioration continuum associated with exposure to neurotoxic substances. Progression of neurotoxic dysfunction is dependent on both the duration and concentration of exposure (dose), and may be influenced by other workplace factors, individual health status and susceptibility as well as lifestyle, particularly drinking and exposure to neurotoxic substances used in hobbies, such as glues applied in furniture assembly or plastic model building, paints and paint removers.

                                                  Figure 1. Health deterioration on a continuum with increasing dosage

                                                  NER040F1

                                                  Different strategies are adopted for identification of neurotoxin-related illness among individual workers and for the surveillance of early nervous system deterioration among active workers. Clinical diagnosis relies on a constellation of signs and symptoms, coupled to the medical and exposure history for an individual; aetiologies other than exposure must be systematically ruled out. For the surveillance of early dysfunction among active workers, the group portrait of dysfunction is important. Most often, the pattern of dysfunction observed for the group will be similar to the pattern of impairment clinically observed in the disease. It is somewhat like summing early, mild alterations to produce a picture of what is happening to the nervous system. The pattern or profile of the overall early response provides an indication of the specificity and the type of action of the particular neurotoxic substance or mixture. In workplaces with potential exposure to neurotoxic substances, health surveillance of groups of workers may prove particularly useful for prevention and workplace action in order to avoid the development of more severe illness (see Figure 2). Workplace studies carried out throughout the world, with active workers exposed to specific neurotoxic substances or to mixtures of various chemicals, have provided valuable information on early manifestations of nervous system dysfunction in groups of exposed workers.

                                                  Figure 2. Preventing neurotoxicity at work.

                                                  NER090F1

                                                  Early symptoms of chronic poisoning

                                                  Altered mood states are most often the first symptoms of the initial changes in nervous system functioning. Irritability, euphoria, sudden mood changes, excessive tiredness, feelings of hostility, anxiousness, depression and tension are among the mood states most often associated with neurotoxic exposures. Other symptoms include memory problems, concentration difficulties, headaches, blurred vision, feelings of drunkenness, dizziness, slowness, tingling sensation in hands or feet, loss of libido and so on. Although in the early stages these symptoms are usually not sufficiently severe to interfere with work, they do reflect diminished well-being and affect one’s capacity to fully enjoy family and social relations. Often, because of the non-specific nature of these symptoms, workers, employers and occupational health professionals tend to ignore them and look for causes other than workplace exposure. Indeed, such symptoms may contribute to or aggravate an already difficult personal situation.

                                                  In workplaces where neurotoxic substances are used, workers, employers and occupational health and safety personnel should be particularly aware of the symptomatology of early intoxication, indicative of nervous system vulnerability to exposure. Symptom questionnaires have been developed for worksite studies and surveillance of workplaces where neurotoxic substances are used. Table 1 contains an example of such a questionnaire.

                                                   


                                                  Table 1. Chronic symptoms checklist

                                                   

                                                  Symptoms experienced in the past month

                                                  1.         Have you tired more easily than expected for the type of activity you do?

                                                  2.         Have you felt light-headed or dizzy?

                                                  3.         Have you had difficulty concentrating?

                                                  4.         Have you been confused or disoriented?

                                                  5.         Have you had trouble remembering things?

                                                  6.         Have your relatives noticed that you have trouble remembering things?

                                                  7.         Have you had to make notes to remember things?

                                                  8.         Have you found it hard to understand the meaning of newspapers?

                                                  9.         Have you felt irritable?

                                                  10.       Have you felt depressed?

                                                  11.       Have you had heart palpitations even when you are not exerting yourself?

                                                  12.       Have you had a seizure?

                                                  13.       Have you been sleeping more often than is usual for you?

                                                  14.       Have you had difficulty falling asleep?

                                                  15.       Have you been bothered by incoordination or loss of balance?

                                                  16.       Have you had any loss of muscle strength in your legs or feet?

                                                  17.       Have you had any loss of muscle strength in your arms or hands?

                                                  18.       Have you had difficulty moving your fingers or grasping things?

                                                  19.       Have you had hand numbness and tingling in your fingers lasting for more than a day?

                                                  20.       Have you had hand numbness and tinging in your toes lasting more than a day?

                                                  21.       Have you had headaches at least once a week?

                                                  22.       Have you had difficulty driving home from work because you felt dizzy or tired?

                                                  23.       Have you felt “high” from the chemicals used at work?

                                                  24.       Have you had a lower tolerance for alcohol (takes less to get drunk)?

                                                  Source: Taken from Johnson 1987.


                                                   

                                                  Early motor, sensory and cognitive changes in chronicpoisoning

                                                  With increasing exposure, changes can be observed in motor, sensory and cognitive functions in workers exposed to neurotoxic substances, who do not present clinical evidence of abnormality. Since the nervous system is complex, and certain areas are vulnerable to specific chemicals, while others are sensitive to the action of a large number of toxic agents, a wide range of nervous system functions may be affected by a single toxic agent or a mixture of neurotoxins. Reaction time, hand-eye coordination, short-term memory, visual and auditory memory, attention and vigilance, manual dexterity, vocabulary, switching attention, grip strength, motor speed, hand steadiness, mood, colour vision, vibrotactile perception, hearing and smell are among the many functions that have been shown to be altered by different neurotoxic substances.

                                                  Important information on the type of early deficits that result from exposure has been provided by comparing performance between exposed and non-exposed workers and with respect to the degree of exposure. Anger (1990) provides an excellent review of worksite neurobehavioural research up to 1989. Table 2 adapted from this article, provides an example of the type of neuro-functional deficits that have been consistently observed in groups of active workers exposed to some of the most common neurotoxic substances.

                                                  Table 2. Consistent neuro-functional effects of worksite exposures to some leading neurotoxic substances

                                                   

                                                  Mixed organic solvents

                                                  Carbon disulphide

                                                  Styrene

                                                  Organophos-
                                                  phates

                                                  Lead

                                                  Mercury

                                                  Acquisition

                                                  +

                                                   

                                                   

                                                  +

                                                   

                                                  Affect

                                                  +

                                                   

                                                  +

                                                   

                                                  +

                                                   

                                                  Categorization

                                                  +

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Coding

                                                  +

                                                  +

                                                   

                                                   

                                                  +

                                                  +

                                                  Colour vision

                                                  +

                                                   

                                                  +

                                                   

                                                   

                                                   

                                                  Concept shifting

                                                  +

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Distractibility

                                                   

                                                   

                                                   

                                                   

                                                  +

                                                   

                                                  Intelligence

                                                  +

                                                  +

                                                   

                                                  +

                                                  +

                                                  +

                                                  Memory

                                                  +

                                                  +

                                                  +

                                                  +

                                                  +

                                                  +

                                                  Motor coordination

                                                  +

                                                  +

                                                  +

                                                   

                                                  +

                                                  +

                                                  Motor speed

                                                  +

                                                  +

                                                  +

                                                   

                                                  +

                                                  +

                                                  Near visual contrast sensitivity

                                                  +

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Odour perception threshold

                                                  +

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Odour identification

                                                  +

                                                   

                                                   

                                                   

                                                  +

                                                   

                                                  Personality

                                                  +

                                                  +

                                                   

                                                   

                                                   

                                                  +

                                                  Spatial relations

                                                  +

                                                  +

                                                   

                                                   

                                                  +

                                                   

                                                  Vibrotactile threshold

                                                  +

                                                   

                                                   

                                                  +

                                                   

                                                  +

                                                  Vigilance

                                                  +

                                                  +

                                                   

                                                   

                                                  +

                                                   

                                                  Visual field

                                                   

                                                   

                                                   

                                                   

                                                  +

                                                  +

                                                  Vocabulary

                                                   

                                                   

                                                   

                                                   

                                                  +

                                                   

                                                  Source: Adapted from Anger 1990.

                                                  Although at this stage in the continuum from well-being to disease, loss is not in the clinically abnormal range, there can be health-related consequences associated with such changes. For example, decreased vigilance and reduced reflexes may put workers in greater danger of accidents. Smell is used to identify leaks and mask saturation (cartridge breakthrough), and acute or chronic loss of smell renders one less apt to identify a potentially hazardous situation. Mood changes may interfere with inter-personal relations at work, socially and in the home. These initial stages of nervous system deterioration, which can be observed by examining groups of exposed workers and comparing them to non-exposed workers or with respect to their degree of exposure, reflect diminished well-being and may be predictive of risk of more serious neurological problems in the future.

                                                  Mental health in chronic poisoning

                                                  Neuropsychiatric disorders have long been attributed to exposure to neurotoxic substances. Clinical descriptions range from affective disorders, including anxiety and depression, to manifestations of psychotic behaviour and hallucinations. Acute high-level exposure to many heavy metals, organic solvents and pesticides can produce delirium. “Manganese madness” has been described in persons with long-term exposure to manganese, and the well-known “mad hatter” syndrome results from mercury intoxication. Type 2a Toxic Encephalopathy, characterized by sustained change in personality involving fatigue, emotional lability, impulse control and general mood and motivation, has been associated with organic solvent exposure. There is growing evidence from clinical and population studies that personality disorders persist over time, long after exposure ceases, although other types of impairment may improve.

                                                  On the continuum from well-being to disease, mood changes, irritability and excessive fatigue are often the very first indications of over-exposure to neurotoxic substances. Although neuropsychiatric symptoms are routinely surveyed in worksite studies, these are rarely presented as a mental health problem with potential consequences on mental and social well-being. For example, changes in mental health status affect one’s behaviour, contributing to difficult inter-personal relationships and disagreements in the home; these in turn can aggravate one’s mental state. In workplaces with employee aid programmes, designed to help employees with personal problems, ignorance of the potential mental health effects of exposure to neurotoxic substances can lead to treatment dealing with the effects rather than the cause. It is interesting to note that among the many reported outbreaks of “mass hysteria” or psychogenic illness, industries with exposure to neurotoxic substances are over-represented. It is possible that these substances, which, for the large part, went unmeasured, contributed to the reported symptoms.

                                                  Mental health manifestations of neurotoxin exposure can be similar to those that are caused by psychosocial stressors associated with poor work organization, as well as psychological reactions to accidents, very stressful occurrences and severe intoxications, called post-traumatic stress disorder (as discussed elsewhere in this Encyclopaedia). A good understanding of the relation between mental health problems and working conditions is important to initiating adequate preventive and curative actions.

                                                  General considerations in assessing early neurotoxicdysfunction

                                                  When evaluating early nervous system dysfunction among active workers, a number of factors must be taken into account. Firstly, many of the neuropsychological and neurophysiological functions that are examined diminish with age; some are influenced by culture or educational level. These factors must be taken into account when considering the relation between exposure and nervous system alterations. This can be done by comparing groups with similar socio-demographic status or by using statistical methods of adjustment. There are, however, certain pitfalls that should be avoided. For example, older workers may have longer work histories, and it has been suggested that some neurotoxic substances may accelerate ageing. Job segregation may confine poorly educated workers, women and minorities in jobs with higher exposures. Secondly, alcohol consumption, smoking and drugs, which all contain neurotoxic substances, may also affect symptoms and performance. A good understanding of the workplace is important in unravelling the different factors that contribute to nervous system dysfunction and the implementation of preventive measures.

                                                   

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                                                  Thursday, 17 February 2011 22:30

                                                  Chemical Neurotoxic Agents

                                                  Definition of Neurotoxicity

                                                  Neurotoxicity refers to the capability of inducing adverse effects in the central nervous system, peripheral nerves or sensory organs. A chemical is considered to be neurotoxic if it is capable of inducing a consistent pattern of neural dysfunction or change in the chemistry or structure of the nervous system.

                                                  Neurotoxicity is generally manifested as a continuum of symptoms and effects, which depend on the nature of the chemical, the dose, the duration of exposure and the traits of the exposed individual. The severity of the observed effects, as well as the evidence for neurotoxicity, increases through levels 1 to 6, shown in Table 1. Short-term or low-dose exposure to a neurotoxic chemical may result in subjective symptoms such as headache and dizziness, but the effect usually is reversible. With increasing dose, neurological changes may show up, and eventually irreversible morphological changes are generated. The degree of abnormality needed for implying neurotoxicity of a chemical agent is a controversial issue. According to the definition, a consistent pattern of neural dysfunction or change in the chemistry or structure of the nervous system is considered if there is well-documented evidence for persistent effects on level 3, 4, 5 or 6 in Table 1. These levels reflect the weight of evidence provided by different signs of neurotoxicity. Neurotoxic substances include naturally occurring elements such as lead, mercury and manganese; biological compounds such as tetrodotoxin (from the puffer fish, a Japanese delicacy) and domoic acid (from contaminated mussels); and synthetic compounds including many pesticides, industrial solvents and monomers.

                                                  Table 1. Grouping neurotoxic effects to reflect their relative strength for establishing neurotoxicity

                                                  Level

                                                  Grouping

                                                  Explanation/Examples

                                                  6

                                                  Morphological changes

                                                  Morphological changes include cell death and axonopathy as well as subcellular morphological changes.

                                                  5

                                                  Neurological changes

                                                  Neurological change embraces abnormal findings in neurological examinations on single individuals.

                                                  4

                                                  Physiological/behavioural changes

                                                  Physiological/behavioural changes comprise experimental findings on groups of animals or humans such as changes in evoked potentials and EEG, or changes in psychological and behavioural tests.

                                                  3

                                                  Biochemical changes

                                                  Biochemical changes cover changes in relevant biochemical parameters (e.g., transmitter level, GFA-protein content (glial fibrillary acidic protein) or enzyme activities).

                                                  21

                                                  Irreversible, subjective symptoms

                                                  Subjective symptoms. No evidence of abnormality on neurological, psychological or other medical examination.

                                                  11

                                                  Reversible, subjective symptoms

                                                  Subjective symptoms. No evidence of abnormality on neurological, psychological, or other medical examination.

                                                  1 Humans only
                                                  Source: Modified from Simonsen et al. 1994.

                                                  In the United States between 50,000 and 100,000 chemicals are in commerce, and 1,000 to 1,600 new chemicals are submitted for evaluation each year. More than 750 chemicals and several classes or groups of chemical compounds are suspected to be neurotoxic (O’Donoghue 1985), but the majority of chemicals have never been tested for neurotoxic properties. Most of the known neurotoxic chemicals available today have been identified by case-reports or through accidents.

                                                  Although neurotoxic chemicals often are produced to fulfil specific uses, exposure may arise from several sources—use in private homes, in agriculture and in industries, or from polluted drinking water and so on. Fixed a priori preconceptions about which neurotoxic compounds are expected to be found in which occupations should therefore be viewed with caution, and the following citations should be looked upon as possible examples including a few of the most common neurotoxic chemicals (Arlien-Søborg 1992; O’Donoghue 1985; Spencer and Schaumburg 1980; WHO 1978).

                                                  Symptoms of Neurotoxicity

                                                  The nervous system generally reacts rather stereotypically to exposure to neurotoxic substances Figure 1. Some typical syndromes are indicated below.

                                                  Figure 1. Neurological and behavioural effects of exposure to neurotoxic chemicals.

                                                  NER030T2

                                                  Polyneuropathy

                                                  This is caused by impairment of motor and sensory nerve function leading to weakness of the muscles, with paresis usually most pronounced peripherally in the upper and lower extremities (hands and feet). Prior or simultaneous paraesthesia (tingling or numbness in the fingers and toes) may occur. This may lead to difficulties in walking or in the fine coordination of hands and fingers. Heavy metals, solvents and pesticides, among other chemicals, may result in such disability, even if the toxic mechanism of these compounds may be totally different.

                                                  Encephalopathy

                                                  This is caused by a diffuse impairment of the brain, and may result in fatigue; impairment of learning, memory and ability to concentrate; anxiety, depression, increased irritability and emotional instability. Such symptoms may indicate early diffuse degenerative brain disorder as well as occupational chronic toxic encephalopathy. Often increased frequency of headaches, dizziness, changes in sleep pattern and reduced sexual activity may also be present from the early stages of the disease. Such symptoms may develop following long-term, low-level exposure to several different chemicals such as solvents, heavy metals or hydrogen sulphide, and are also seen in several dementing disorders not related to work. In some cases more specific neurological symptoms can be seen (e.g., Parkinsonism with tremor, rigidity of the muscles and slowing of movements, or cerebellar symptoms such as tremor and reduced coordination of hand movements and gait). Such clinical pictures can be seen following exposure to some specific chemicals such as manganese, or MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) in the former condition, and toluene or mercury in the latter.

                                                  Gases

                                                  A wide variety of chemicals with totally different chemical structures are gases at normal temperature and have been proven neurotoxic Table 3. Some of them are extremely toxic even in very small doses, and have even been used as war gases (phosgene and cyanide); others require high doses over longer periods to give symptoms (e.g., carbon dioxide). Some are used for general anaesthesia (e.g., nitrous oxide); others are widely used in industry and in agents used for disinfection (e.g., formaldehyde). The former may induce irreversible changes in the nervous system after repeated low-level exposure, the latter apparently produce only acute symptoms. Exposure in small rooms with poor ventilation is particularly hazardous. Some of the gases are odourless, which makes them particularly dangerous (e.g., carbon monoxide). As shown in Table 2, some gases are important constituents in industrial production, while others are the result of incomplete or complete combustion (e.g., CO and CO2 respectively). This is seen in mining, steel works, power stations and so on, but may also be seen in private homes with insufficient ventilation. Essential for treatment is to stop further exposure and provide fresh air or oxygen, and in severe cases artificial ventilation.

                                                  Table 2. Gases associated with neurotoxic effects

                                                  Chemical

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Carbon dioxide (CO2 )

                                                  Welding; fermentation; manufacture, storage and use of dry ice

                                                  Metal industry; mining; breweries

                                                  M: Dilate vessels

                                                  A: Headache; dyspnoea; tremor; loss of consciousness

                                                  C: Hardly any

                                                  Carbon monoxide (CO)

                                                  Car repair; welding; metal melting; drivers; firemen

                                                  Metal industry; mining; transportation; power station

                                                  M: Deprivation of oxygen

                                                  A: Headache; drowsiness; loss of consciousness

                                                  Hydrogen sulphide (H2S)

                                                  Fumigating of green house; manure; fishermen; fish unloading; sewerage handling

                                                  Agriculture; fishing; sewer work

                                                  M: Blocking oxidative metabolism

                                                  A: Loss of consciousness

                                                  C: Encephalopathy

                                                  Cyanide (HCN)

                                                  Electro-welding; galvanic surface treatment with nickel; copper and silver; fumigation of ships, houses foods and soil in green houses

                                                  Metal industry; chemical industry; nursery; mining; gasworks

                                                  M: Blocking of respiratory enzymes

                                                  A: Dyspnoea; falling blood pressure; convulsions; loss of consciousness; death

                                                  C: Encephalopathy; ataxia; neuropathy (e.g., aftereating cavasava)

                                                  Occupational impairment uncertain

                                                  Nitrous oxide (N2O)

                                                  General anaesthesia during operation; light narcosis at dental care and delivery

                                                  Hospitals (anaesthesia); dentists; midwife

                                                  M: Acute change in nerve cell membrane; degeneration of nerve cells after long-term exposure

                                                  A: Light-headedness; drowsiness; loss of consciousness

                                                  C: Numbness of fingers and toes; reduced coordination; encephalopathy

                                                  1 M: mechanism; A: acute effects; C: chronic effects.
                                                  Neuropathy: dysfunction of motor- and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain.
                                                  Ataxia: impaired motor coordination.

                                                   

                                                  Metals

                                                  As a rule the toxicity of metals increases with increasing atomic weight, lead and mercury being particularly toxic. Metals are usually found in nature at low concentrations, but in certain industries they are used in great amounts (see Table 3) and may give rise to occupational risk for the workers. Moreover, considerable amounts of metals are found in waste water and may give rise to environmental risk for the residents close to the plants but also at greater distances. Often the metals (or, for example, organic mercury compounds) are taken up into the food chain and will accumulate in fish, birds and animals, representing a risk for consumers. The toxicity and the way in which the metals are handled by the organism may depend on the chemical structure. Pure metals may be taken up by inhalation or skin contact of vapour (mercury) and/or small particles (lead), or orally (lead). Inorganic mercury compounds (e.g., HgCl2) are mainly taken up by mouth, while organic metal compounds (e.g., tetraethyl lead) mainly are taken up by inhalation or by skin contact. The body burden may to a certain degree be reflected in the concentration of metal in the blood or urine. This is the basis for biological monitoring. In treatment it must be recalled that especially lead is released very slowly from deposits in the body. The amount of lead in bones will normally be reduced by only 50% over 10 years. This release may be speeded up by the use of chelating agents: BAL (dimercapto-1-propanol), Ca-EDTA or penicillamine.

                                                  Table 3. Metals and their inorganic compounds associated with neurotoxicity

                                                  Chemical

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Lead

                                                  Melting; soldering; grinding; repair; glazing; plasticizer

                                                  Metal work; mining; accumulator plants; car repair; shipyards; glass workers; ceramics; pottery; plastic

                                                  M: Impairment of oxidative metabolism of nerve cells and glia

                                                  A: Abdominal pain; headache; encephalopathy; seizures

                                                  C: Encephalopathy; polyneuropathy, including drop hand

                                                  Mercury Elemental

                                                  Electrolysis; electrical instruments (gyroscope; manometer; thermometer; battery; electric bulb; tubes, etc.); amalgam filling

                                                  Chloralkali plants; mining; electronics; dentistry; polymer production; paper and pulp industry

                                                  M: Impairment at multiple sites in nerve cells

                                                  A: Lung inflammation; headache; impaired speech

                                                  C: Inflammation of gums; appetite loss; encephalopathy; including tremor; irritability

                                                  Calomel Hg2Cl2

                                                   

                                                  Laboratories

                                                  A: Low acute toxicity chronic toxic effects, see above

                                                  Sublimate HgCl2

                                                  Disinfection

                                                  Hospitals; clinics; laboratories

                                                  M: Acute tubular and glomerular renal degeneration. Verytoxic even in small oral doses, lethal down to 30 mg/kgweight

                                                  C: See above.

                                                  Manganese

                                                  Melting (steel alloy); cutting; welding in steel; dry batteries

                                                  Manganese mining; steel and aluminium production; metal industry; battery production; chemical industry; brickyard

                                                  M: Not known, possible changes in dopamine and catecholamine in basal ganglia in the centre of the brain

                                                  A: Dysphoria

                                                  C: Encephalopathy including Parkinsonism; psychosis; appetite loss; irritability; headache; weakness

                                                  Aluminium

                                                  Metallurgy; grinding; polishing

                                                  Metal industry

                                                  M: Unknown

                                                  C: Possibly encephalopathy

                                                  1 M: mechanism; A: acute effects; C: chronic effects.
                                                  Neuropathy: dysfunction of motor- and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain.

                                                   

                                                  Monomers

                                                  Monomers constitute a large, heterogeneous group of reactive chemicals used for chemical synthesis and production of polymers, resins and plastics. Monomers comprise polyhalogenated aromatic compounds such as p-chlorobenzene and 1,2,4-trichlorbenzene; unsaturated organic solvents such as styrene and vinyltoluene, acrylamide and related compounds, phenols, ɛ-caprolactam and ζ-aminobutyrolactam. Some of the widely used neurotoxic monomers and their effect on the nervous system are listed in Table 3. Occupational exposure to neurotoxic monomers may take place at industries manufacturing, transporting and using chemical products and plastic products. During handling of polymers containing rest monomers, and during moulding in boat yards and in dental clinics, a substantial exposure to neurotoxic monomers takes place. Upon exposure to these monomers uptake may take place during inhalation (e.g., carbon disulphide and styrene) or by skin contact (e.g., acrylamide). As monomers are a heterogeneous group of chemicals, several different mechanisms of toxicity are likely. This is reflected by differences in symptoms (Table 4).

                                                  Table 4. Neurotoxic monomers

                                                  Compound

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Acrylamide

                                                  Employees exposed to the monomer

                                                  Polymer production; tunnelling and drilling operations

                                                  M: Impaired axonal transport

                                                  C: Polyneuropathy; dizziness; tremor and ataxia

                                                  Acrylonitrile

                                                  Accidents in labs and industries; house fumigation

                                                  Polymer and rubber production; chemical synthesis

                                                  A: Hyperexcitability; salivation; vomiting; cyanosis; ataxia; difficulty breathing

                                                  Carbon disulphide

                                                  Production of rubber and viscose rayon

                                                  Rubber and viscose rayon industries

                                                  M: Impaired axonal transport and enzyme activity is likely

                                                  C: Peripheral neuropathy; encephalopathy; headache; vertigo; gastrointestinal disturbances

                                                  Styrene

                                                  Production of glass-reinforced plastics; monomer manufacture and transportation; use of styrene-containing resins and coatings

                                                  Chemical industry; fibreglass production; polymer industry

                                                  M: Unknown

                                                  A: Central nervous system depression; headache

                                                  C: Polyneuropathy; encephalopathy; hearing loss

                                                  Vinyltoluene

                                                  Resin production; insecticide compounds

                                                  Chemical and polymer industry

                                                  C: Polyneuropathy; reduced motor nerve conductionvelocity

                                                  1 M: mechanism; A: acute effects; C: chronic effects.
                                                  Neuropathy: dysfunction of motor and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain.
                                                  Ataxia: impaired motor coordination.

                                                   

                                                  Organic solvents

                                                  Organic solvents is a common designation for a large group of more than 200 lipophilic chemical compounds capable of dissolving fats, oils, waxes, resins, rubber, asphalt, cellulose filaments and plastic materials. They are usually fluids at room temperature with boiling points below 200 to 250°C, and are easily evaporated. They are mainly taken up via the lungs but some may penetrate the skin as well. Due to their lipophilicity they are distributed to organs rich in fat. Thus high concentrations are found in body fat, bone marrow, liver and brain, which also may act as reservoirs of solvents. The partition coefficient octanol/water can indicate whether high brain concentrations are to be expected. The mechanism of toxicity is not yet known, but several possibilities have been envisioned: blocking important enzymes in the metabolic breakdown of glucose and thus reducing energy available for neuronal processing; reducing energy formation in the mitochondria; changing neuronal membranes, leading to impairment of ion channel function; slowing of axonal flow. Methylene chloride is metabolized to CO, which blocks the transport of oxygen in the blood. Large groups of workers in a great variety of professions are exposed daily or at least frequently (see Table 5). In some countries the consumption of organic solvents has declined in some occupations due to hygienic improvements and substitution (e.g., house painters, graphic industry workers, metal workers), while in other occupations the pattern of exposure has changed but the total amount of organic solvents has remained unchanged. For example, trichloroethylene has been replaced by 1,1,1-trichloroethane and freon. So solvents are still a major hygienic problem at many workplaces. People are at particular risk when exposed in small rooms with poor ventilation and with high temperature, increasing the evaporation. Physical work increases the pulmonary uptake of solvents. In several countries (in particular the Nordic countries), compensation has been given to workers who have developed chronic toxic encephalopathy following long-term, low-level exposure to solvents.

                                                  Table 5. Organic solvents associated with neurotoxicity

                                                  Chemical

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Chlorinated hydrocarbons: trichloroethylene;

                                                  1,1,1-trichloroethane; tetrachloroethylene

                                                  Degreasing; electroplating; painting; printing; cleaning; general and light anaesthesia

                                                  Metal industry; graphic industry; electronic industry; dry cleaners; anaesthetists

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy; polyneuropathy; trigeminal affection (TRI); hearing loss

                                                  Methylene chloride

                                                  Extraction, including extraction of caffeine; paint remover

                                                  Food industry; painters; graphic industry

                                                  M: Metabolism ® CO

                                                  A: Prenarcotic symptoms; coma

                                                  C: Encephalopathy

                                                  Methyl chloride

                                                  Refrigerator production and repair

                                                  Refrigerator production; rubber industry; plastic industry

                                                  M: Unknown

                                                  A: Prenarcotic symptoms; loss of consciousness; death

                                                  C: Encephalopathy

                                                  Toluene

                                                  Printing; cleaning; degreasing; electroplating; painting; spray painting

                                                  Graphic industry; electronic industry

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy; cerebellar dysfunction; polyneuropathy; hearing loss; visual disturbance

                                                  Xylene

                                                  Printing; synthesis of phthalic anhydride; painting; histology laboratory procedures

                                                  Graphic industry; plastic industry; histology laboratories

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy; visual disturbance; hearing loss

                                                  Styrene

                                                  Polymerization; moulding

                                                  Plastic industry; fibreglass production

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy; polyneuropathy; hearing loss

                                                  Hexacarbons: n-hexane;

                                                  methyl butyl ketone (MBK);

                                                  methyl ethyl ketone (MEK)

                                                  Gluing; printing; plastic coating; painting; extraction

                                                  Leather and shoe industry; graphic industry; painter; laboratories

                                                  M: Impairment of axonal transport

                                                  A: Prenarcotic

                                                  C: Polyneuropathy; encephalopathy

                                                  Various solvents: Freon 113

                                                  Refrigerator production and repair; dry cleaning; degreasing

                                                  Refrigerator production; metal industry; electronic industry; dry cleaning

                                                  M: Unknown

                                                  A: Mild prenarcotic symptoms

                                                  C: Encephalopathy

                                                  Diethylether; halothane

                                                  General anaesthetics (nurses; doctors)

                                                  Hospitals; clinics

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy

                                                  Carbon disulphide

                                                  See monomers

                                                  See monomers

                                                  See monomers

                                                  Mixtures: white spirit and thinner

                                                  Painting; degreasing; cleaning; printing; impregnation; surface treatment

                                                  Metal industry; graphic industry; wood industry; painters

                                                  M: Unknown

                                                  A: Prenarcotic symptoms

                                                  C: Encephalopathy

                                                   1 M: mechanism; A: acute effects; C: chronic effects.

                                                  Neuropathy: dysfunction of motor- and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain

                                                   

                                                  Pesticides

                                                  Pesticides is used as a generic term for any chemical designed to kill groups of plants or animals that are a human health hazard or may cause economic loss. It includes insecticides, fungicides, rodenticides, fumigants and herbicides. Approximately 5 billion pounds of pesticide products made up of more than 600 active pesticide ingredients are annually used in agriculture worldwide. Organophosphorus, carbamate and organochlorine pesticides together with pyrethroids, chlorophenoxy herbicides and organic metal compounds used as fungicides have neurotoxic properties (Table 6). Among the many different chemicals used as rodenticides, some (e.g., strychnine, zinc phosphide and thallium) are neurotoxic too. Occupational exposure to neurotoxic pesticides is mainly associated with agricultural work such as pesticide handling and working with treated crops, but exterminators, pesticide manufacturing and formulating employees, highway and railway workers, as well as greenhouse, forestry and nursery workers may have a substantial risk of being exposed to neurotoxic pesticides as well. Children, who constitute a significant proportion of the agricultural workforce, are especially vulnerable because their nervous systems are not fully developed. The acute effects of pesticides are generally well described, and long-lasting effects upon repeated exposure or single high dose exposure are often seen (Table 6), but the effect of repeated subclinical exposure is uncertain.

                                                  Table 6. Classes of common neurotoxic pesticides, exposure, effects and associated symptoms

                                                  Compound

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Organo-phosphorus compounds: Beomyl; Demethon; Dichlorvos; Ethyl parathion; Mevinphos; Phosfolan; Terbufos; Malathion

                                                  Handling; treatment of crops; working with treated crops; dock labourer

                                                  Agriculture; forestry; chemical; gardening

                                                  M: Acetyl cholinesterase inhibition

                                                  A: Hyperactivity; neuromuscular paralysis; visual impairment; breathing difficulty; restlessness; weakness; vomiting; convulsions

                                                  Carbamates: Aldicarb; Carbaryl; Carbofuran; Propoxur

                                                     

                                                  M: Delayed neurotoxicity axonopathy2

                                                  C: Polyneuropathy; numbness and tingling in feet; muscle weakness; sensory disturbance; paralysis

                                                  Organochlorine: Aldrin; Dieldrin; DDT; Endrin; Heptachlor; Lindane; Methoxychlor; Mirex; Toxaphene

                                                  See above

                                                  See above

                                                  A: Excitability; apprehension; dizziness; headache; confusion; loss of balance; weakness; ataxia; tremors; convulsions; coma

                                                  C: Encephalopathy

                                                  Pyrethroids

                                                  See above

                                                  See above

                                                  M: Altering flow of sodium ions through nerve cellmembrane

                                                  A: Repeated firing of the nerve cell; tremor; convulsion

                                                  2,4-D

                                                  Herbicide

                                                  Agriculture

                                                  C: Polyneuropathy

                                                  Triethyltin hydroxide

                                                  Surface treatment; handling treated wood

                                                  Wood and wood products

                                                  A: Headache; weakness; paralysis; visual disturbances

                                                  C: Polyneuropathy; CNS effects

                                                  Methyl bromide

                                                  Fumigating

                                                  Greenhouses; insecticide; manufacture of refrigerators

                                                  M: Unknown

                                                  A: Visual and speech disturbances; delirium; convulsion

                                                  C: Encephalopathy

                                                  1 M: mechanism; A: acute effects; C: chronic effects.
                                                  Neuropathy: dysfunction of motor and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain.
                                                  Ataxia: impaired motor coordination.
                                                  2 Mainly phosphates or phosphonates.

                                                   

                                                  Other chemicals

                                                  Several different chemicals which do not fit into the above-mentioned groups also possess neurotoxicity. Some of these are used as pesticides but also in different industrial processes. Some have well-documented acute and chronic neurotoxic effects; others have obvious acute effects, but the chronic effects are only poorly examined. Examples of these chemicals, their uses and effects are listed in Table 7.

                                                  Table 7. Other chemicals associated with neurotoxicity

                                                  Chemical

                                                  Examples of source of exposure

                                                  Selected industries at risk

                                                  Effects1

                                                  Boric acid

                                                  Welding; fluxes; preservation

                                                  Metal; glass

                                                  A: Delirium; convulsion

                                                  C: CNS depression.

                                                  Disulfiram

                                                  Pharmaceutical

                                                  Rubber

                                                  C: Fatigue; peripheral neuropathy; sleepiness

                                                  Hexachlorophene

                                                  Antibacterial soaps

                                                  Chemical

                                                  C: CNS oedema; peripheral nerve damage

                                                  Hydrazine

                                                  Reducing agents

                                                  Chemical; army

                                                  A: Excitement; appetite loss; tremor; convulsion

                                                  Phenol/Cresol

                                                  Antiseptics

                                                  Plastics; resins; chemical; hospitals; laboratories

                                                  M: Denatures proteins and enzymes

                                                  A: Reflex loss; weakness; tremor; sweating; coma

                                                  C: Appetite loss; mental disturbance; ringing in the ears

                                                  Pyridine

                                                  Ethanol denaturation

                                                  Chemical; textile

                                                  A: CNS depression; mental depression; fatigue; appetite loss

                                                  C: Irritability; sleep disorders; polyneuropathy; double vision

                                                  Tetraethyl lead

                                                  Gasoline additive

                                                  Chemical; transport

                                                  C: Irritability; weakness; tremor; vision difficulties

                                                  Arsine

                                                  Batteries; insecticide; melting

                                                  Smelting; glasswork; ceramics;  manufacture of paper

                                                  M: Impairing enzyme function

                                                  A: Reduced sensation; paresis; convulsion; coma

                                                  C: Motor impairment; ataxia; vibration sense loss; polyneuropathy

                                                  Lithium

                                                  Oil additive; pharmaceutical

                                                  Petrochemical

                                                  A/C: Appetite loss; ringing in the ears; vision blurring; tremor; ataxia

                                                  Selenium

                                                  Melting; production of rectifiers; vulcanization; cutting oils; antioxidant

                                                  Electronic; glass works; metal industry; rubber industry

                                                  A: Delirium; anosmia

                                                  C: Odour of garlic; polyneuropathy; nervousness

                                                  Thallium

                                                  Rodenticide

                                                  Glass; glass products

                                                  A: Appetite loss; tiredness; drowsiness; metallic taste; numbness; ataxia

                                                  Tellurium

                                                  Melting; rubber production; catalyst

                                                  Metal; chemical; rubber; electronic

                                                  A: Headache; drowsiness; neuropathy

                                                  C: Odour of garlic; metallic taste; Parkinsonism; depression

                                                  Vanadium

                                                  Melting

                                                  Mining; steel production; chemical industry

                                                  A: Appetite loss; ringing in the ears; somnolence, tremor

                                                  C: Depression; tremor; blindness

                                                  1 M: mechanism; A: acute effects; C: chronic effects.
                                                  Neuropathy: dysfunction of motor and sensory peripheral nerve fibres.
                                                  Encephalopathy: brain dysfunction due to generalized impairment of the brain.
                                                  Ataxia: impaired motor coordination

                                                   

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                                                  Thursday, 17 February 2011 21:59

                                                  Anatomy and Physiology

                                                  Nerve cells are the functional units of the nervous system. The nervous system is believed to have ten thousand million of such cells, called neurons and glia, the glia being present in greater numbers than neurons.

                                                  The Neuron

                                                  Figure 1 is an idealized diagram of a neuron with its three most important structural features: the cell body, the dendrites and the axon terminal.

                                                  Figure 1. The anatomy of the neuron

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                                                  The dendrites are finely branched processes arising near the cell body of a neuron. The dendrites receive excitatory or inhibitory effects via chemical messengers called neurotransmitters. The cytoplasm is the material of the cell body in which the organelles—including the cell nucleus—and other inclusions are found Figure 2. The nucleus contains the cell’s chromatin, or genetic material.

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Figure 2. The organelles

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                                                  The nucleus of the nerve cell is atypical compared with that of other living cells in that, although it contains the genetic material deoxyribonucleic acid (DNA), the DNA is not involved in the process of cell division; that is, after reaching maturity, nerve cells do not divide. (An exception to this rule are the neurons in the nose lining (olfactory epithelium).) The nucleus is rich in ribonucleic acid (RNA), which is necessary for the synthesis of protein. Three types of proteins have been identified: cytosolic proteins, which form the fibrillar elements of the nerve cell; intracondrial proteins, which generate energy for cell activity; and proteins that form membranes and secretory products. Neurons are now conceived of as modified secretory cells. Secretory granules are formed, stored in synaptic vesicles and later released as neurotransmitter substances, the chemical messengers between nerve cells.

                                                  The fibrillar elements, which form the skeleton of the neuron, participate in the trophic function of the neuron, acting as vehicles of transmission. Axonal transport can be anterograde (cell body to axon terminal) and retrograde (axon terminal to cell body). From the thickest to the thinnest, three types of fibrillar elements are recognized: microtubules, neurofilaments and microfilaments.

                                                  Glial Cells

                                                  In contrast to neurons, glial cells do not, by themselves, carry electrical messages. There are two types of glial cells: the macroglia and the microglia. The macroglia is a name given to at least three types of cells: astrocytes, oligodendrocytes and ependymal cells. Microglial cells are primarily scavenger cells for removing debris after neural damage or infection has occurred.

                                                  The glial cells also have distinctive microscopic and ultramicroscopic features. Glial cells physically support neurons, but a number of physiological properties are also now beginning to be understood. Among the most important neuron-glial interactions are the glial cell’s role in providing the neurons with nutrients, removing fragments of neurons after their death and, most importantly, contributing to the process of chemical communication. Glial cells, in sharp contrast to neurons, can divide and thus can reproduce themselves. Tumours of the nervous system, for example, result from an abnormal reproduction of glial cells.

                                                  Myelin

                                                  What appears in the macroscopic observation of neural tissue as “grey matter” and “white matter” has a microscopic and biochemical basis. Microscopically, the grey matter contains the neuronal cell bodies, whereas the white matter is where neural fibres or axons are found. The “white” appearance is due to a sheath—composed of a fatty substance called myelin—covering these fibres. Myelin of the peripheral nerves originates from the membrane of the Schwann cell which wraps around the axon. The myelin of fibres in the central nervous system is provided by the membranes of the oligodendrocytes (a variety of glial cells). Oligodendrocytes usually myelinate several axons, whereas the Schwann cell is associated with only one axon. A discontinuity of the myelin sheath—designated as nodes of Ranvier—exists between continuous Schwann cells or oligodendrocytes. It is estimated that in the longest central motor pathway, up to 2,000 Schwann cells form the myelin cover. Myelin, whose role is to facilitate the propagation of the action potential, may be a specific target of neurotoxic agents. A morphological classification of neurotoxic substances describes characteristic neuropathological changes of the myelin as myelinopathies.

                                                  Trophic Function of the Neuron

                                                  The normal functions of the neuron include protein synthesis, axonal transport, generation and conduction of the action potential, synaptic transmission, and formation and maintenance of the myelin. Some of the basic trophic functions of the neuron were described as early as the 19th century by sectioning the axons (axotomy). Among the processes uncovered, one of the most important was the Wallerian degeneration—after Waller, the English physiologist who described it.

                                                  Wallerian degeneration provides a good opportunity to describe well-known changes in organelles as a result of either traumatic or toxic damage. Parenthetically, the terms used to describe Wallerian degeneration produced by traumatic axotomy are the same ones used to describe changes resulting from neurotoxic agents. At the cellular level, neuropathological changes resulting from toxic damage to neural tissue are far more complex than those occurring as a result of traumatic damage. It is only recently that changes in neurons affected by neurotoxic agents have been observed.

                                                  Twenty-four hours after cutting of the axon, the most distinctive feature is swelling of both sides of the mechanical trauma. Swelling results from accumulation of fluids and membranous elements on both sides of the site of injury. These changes are not unlike those observed in a rain-flooded two-way road with vehicles stopped on both sides of the flooded area. In this analogy, stalled vehicles are the swelling. After a few days, regeneration of the ensheathed axons—i.e., those covered with myelin—occurs. Sprouts grow from the proximal stump moving at the rate of 1 to 3 mm per day. Under favourable conditions, sprouts reach the distal (farther from the cell body) stump. When renervation—joining of the stumps—is completed, the basic features of normal transmission have been re-established. The cell body of the injured neuron undergoes profound structural changes in protein synthesis and axonal transport.

                                                  If molecular neurobiology is said to be a young discipline, the neurobiology of the neurotoxic processes is even younger, and still in its infancy. True, the molecular basis of action of many neurotoxins and pharmacological agents is now well understood. But with some notable exceptions (e.g., lead, methyl mercury, acrylamide) the molecular basis of toxicity of the vast majority of environmental and neurotoxic agents is unknown. That is why, instead of describing the molecular neurobiology of a select group of occupational and environmental neurotoxic agents, we still are forced to refer to the comparatively abundant strategies and examples from classical neuropharmacology or from work in modern drug manufacture.

                                                  Neurotransmitters

                                                  A neurotransmitter is a chemical substance which, when released from axon terminals by the action potential, produces the momentary change in electrical potential when another nerve fibre is stimulated. Neurotransmitters stimulate or inhibit adjacent neurons or effector organs such as muscle and glands. Known neurotransmitters and their neural pathways are now being intensively studied, and new ones are constantly being discovered. Some neurological and psychiatric disorders are now understood to be caused by chemical changes in neurotransmission—for example, myasthenia gravis, Parkinson’s disease, certain forms of affective disorders such as depression, severe distortion of thought processes such as in schizophrenia, and Alzheimer’s disease. Although excellent isolated reports on the effect of several environmental and occupational neurotoxic agents on neurotransmission have been published, the body of knowledge is meagre compared with that existing for neuropsychiatric diseases. Pharmacological studies of manufactured drugs require an understanding of how drugs affect neurotransmission. Drug manufacture and neurotransmission research are thus intimately related. The changing views of drug action have been summarized by Feldman and Quenzer (1984).

                                                  The effects of neurotoxic agents on neurotransmission are characterized by where in the nervous system they act, their chemical receptors, the time course of their effects, whether neurotoxic agents facilitate, block or inhibit neurotransmission, or whether neurotoxic agents alter the termination or removal of the neurotransmitter’s pharmacological action.

                                                  One difficulty experienced by neuroscientists is the need to link known processes that occur at the molecular level in the neuron with events at the cellular level, which in turn may explain how normal and pathological neuropsychological changes occur, as clearly stated in the following which to a large extent still applies: “(A)t the molecular level, an explanation of the action of a drug is often possible; at the cellular level, an explanation is sometimes possible, but at a behavioural level, our ignorance is abysmal” (Cooper, Bloom and Roth 1986).

                                                  The Main Components of the Nervous System

                                                  Knowledge of the main components of the nervous system is essential for the understanding of the gross neuropsychological manifestations of neurotoxic illness, the rationale for the use of specific techniques for the assessment of nervous system functions, and the understanding of pharmacological mechanisms of neurotoxic action. From a functional standpoint, the nervous system can be divided into two major compartments: The somatic nervous system conveys sensory information (touch, temperature, pain and limb position—even when the eyes are closed) from the body segments and carries the neural pathways that innervate and control the movement of skeletal muscles, such as those of the arms, fingers, legs and toes. The visceral nervous system controls internal organs that are not normally under the influence of blood vessels, the dilation and constriction of the pupils of the eyes and so on.

                                                  From an anatomical viewpoint, four main components need to be identified: the central nervous system, the peripheral nervous system including cranial nerves, the autonomic system and the neuroendocrine system.

                                                  The Central Nervous System

                                                  The central nervous system contains the brain and the spinal cord Figure 3. The brain lies in the skull cavity and is protected by the meninges. It is divided into three major components; in ascending order—that is, from the caudal (tail) to cervical (head) portion of the nervous system—they are the hindbrain (also called, the rhombencephalon), the midbrain (the mescencephalon) and the forebrain (the proscencephalon).

                                                  Figure 3. The central and peripheral divisions of the nervous system

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                                                  The hindbrain

                                                  The three major components of the hindbrain are the medulla oblongata, the pons and the cerebellum figure 4.

                                                  Figure 4. The brain shown from a lateral side.

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                                                  The medulla oblongata contains neural structures that control heart rate and breathing, sometimes the targets of neurotoxic agents and drugs causing death. Located between the medulla oblongata and the midbrain, the pons (bridge) derives its names from the large number of fibres traversing its anterior aspect en route to the cerebellar hemispheres. The cerebellum—in Latin, little brain—is characteristically corrugated in appearance. The cerebellum receives sensory information and sends motor messages essential for motor coordination. It is responsible (among other functions) for the execution of fine movements. This scheduling—or programming—requires the adequate timing of sensory inputs and motor responses. The cerebellum is often the target of numerous neurotoxic agents—for example, alcoholic beverages, many industrial solvents, lead—which affect motor responses.

                                                  The midbrain

                                                  The midbrain is a narrow part of the brain connecting the hindbrain to the forebrain. Structures of the midbrain are the cerebral aqueduct, the tectum, the cerebral peduncles, the substantia nigra and the red nucleus. The cerebral aqueduct is a channel that connects the third with the fourth ventricles (liquid-filled cavities of the brain); the cerebrospinal fluid (CSF) flows through this opening.

                                                  The forebrain

                                                  This part of the brain is subdivided into diencephalon (“between brain”) and the cerebrum. The major regions of the diencephalon are the thalamus and the hypothalamus. “Thalamus” means “inner room”. The thalami are made up of neuronal groupings, called nuclei, which have five main functions:

                                                  • receiving sensory information and sending it to primary areas of the cerebral cortex
                                                  • sending information about ongoing movement to motor areas of the cerebral cortex
                                                  • sending information on the activity of the limbic system to areas of the cerebral cortex related to this system
                                                  • sending information on intrathalamic activity to association areas of the cerebral cortex
                                                  • sending information of brain-stem reticular formation activity to widespread areas of the cerebral cortex.

                                                   

                                                  The name hypothalamus means “under the thalamus”. It forms the base of the third ventricle, an important reference point for the imaging of the brain. The hypothalamus is a complex, minute neural structure responsible for many aspects of behaviour such as basic biological drives, motivation and emotion. It is the link between the nervous and the neuroendocrine system, to be reviewed below. The pituitary gland (also called the hypophysis) is linked by neurons to the hypothalamic nuclei. It is well established that the hypothalamic nerve cells perform many neurosecretory functions. The hypothalamus is linked with many other major regions of the brain including the rhinencephalon—the primitive cortex originally associated with olfaction—and the limbic system, including the hippocampus.

                                                  The cerebral cortex is the largest component of the brain, consisting of two cerebral hemispheres connected by a mass of white matter called the corpus callosum. The cerebral cortex is the surface layer of each cerebral hemisphere. Deep sulci in the cerebral cortex—the central and the lateral sulci Figure 4 —are taken as reference points to separate anatomical regions of the brain. The frontal lobe lies in front of the central sulcus. The parietal lobe begins at the back of the central sulcus, and lies next to the occipital lobe, which occupies the posterior portion of the brain. The temporal lobe begins well inside the folding of the lateral sulcus and extends into the ventral aspects of the brain hemispheres. Two important components of the cerebrum are the basal ganglia and the limbic system.

                                                  The basal ganglia are nuclei—that is, clusters of nerve cells—located toward the centre of the brain. The basal ganglia comprise major centres of the extra-pyramidal motor system. (The pyramidal system, to which the term is contrasted, is involved in the voluntary control of movement.) The extrapyramidal system is selectively affected by many neurotoxic agents (e.g., manganese). In the past two decades, important discoveries have been made concerning the role these nuclei play in several neural degenerative diseases (e.g., Parkinson’s disease, Huntington’s chorea).

                                                  The limbic system is comprised of convoluted neural structures branching out into many directions and establishing connections with many “old” regions of the brain, particularly with the hypothalamus. It is involved in the control of emotional expression. The hippocampus is believed to be a structure where many memory processes occur.

                                                  The spinal cord

                                                  The spinal cord is a whitish structure situated within the vertebral canal. It is divided into four regions: cervical, thoracic, lumbar and sacral-coccyxeal. The two most easily recognizable features of the spinal cord are the grey matter containing the cell bodies of the neurons, and the white matter containing the myelinated axons of the neurons. The ventral region of the spinal cord’s grey matter contains nerve cells that regulate motor function; the middle region of the thoracic spinal cord is associated with autonomic functions. The dorsal portion receives sensory information from the spinal nerves.

                                                  The Peripheral Nervous System

                                                  The peripheral nervous system includes those neurons that are outside the central nervous system. The term peripheral describes the anatomical distribution of this system, but functionally it is artificial. The cell bodies of peripheral motor fibres, for example, are located within the central nervous system. In experimental, clinical and epidemiological neurotoxicology, the term peripheral nervous system (PNS) describes a system that is selectively vulnerable to the effects of toxic agents and that is able to regenerate.

                                                  The spinal nerves

                                                  The ventral and dorsal roots are where the peripheral nerves enter and leave the spinal cord along its length. Adjoining vertebrae contain openings to allow root fibres forming the spinal nerves to leave the spinal canal. There are 31 pairs of spinal nerves, which are named according to the region of the vertebral column with which they are associated: 8 cervical, 12 thoracic, 5 lumbar, 5 sacral and 1 coccyxeal. A metamera is a region of the body innervated by a spinal nerve figure 5.

                                                  Figure 5.    The segmental distribution of the spinal nerves (the metamera).

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                                                  Carefully examining the motor and sensory functions of metamerae, neurologists can infer the location of lesions where damage has occurred.

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                   

                                                  Table 1. Names and main functions of each pair of cranial nerves

                                                  Nerve1 Conducts impulses Functions
                                                  I. Olfactory From nose to brain Sense of smell
                                                  II. Optic From eye to brain Vision
                                                  III. Oculomotor From brain to eye muscles Eye movements
                                                  IV. Trochlear From brain to external eye muscles Eye movements
                                                  V. Trigeminal
                                                  (or trifacial)
                                                  From skin and mucous membrane of head and from teeth to brain; also from brain to chewing muscles Sensations of face, scalp and teeth; chewing movements
                                                  VI. Abducens From brain to external eye muscles Turning eyes outward
                                                  VII. Facial From taste buds of tongue to brain; from brain to face muscles Sense of taste; contraction of muscles of facial expression
                                                  VIII. Acoustic From ear to brain Hearing; sense of balance
                                                  IX. Glossopharyngeal From throat and taste buds of tongue to brain; also from brain to throat muscles and salivary glands Sensations of throat, taste, swallowing movements, secretion of saliva
                                                  X. Vagus From throat, larynx, and organs in thoracic and abdominal cavities to brain; also from brain to muscles of throat and to organs in thoracic and abdominal cavities Sensations of throat, larynx, and for thoracic and abdominal organs; swallowing, voice production, slowing of heartbeat, acceleration of peristalsis
                                                  XI. Spinal accessory From brain to certain shoulder and neck muscles Shoulder movements; turning movements of head
                                                  XII. Hypoglossal From brain to muscles of tongue Tongue movements

                                                  1 The first letter of the words of the following sentence are the first letters of the names of cranial nerves: “On Old Olympus’ Tiny Tops A Finn and German Viewed Some Hops”. Many generations of students have used this or a similar sentence to help them remember the names of cranial nerves.

                                                   

                                                  The cranial nerves

                                                  Brain stem is a comprehensive term that designates the region of the nervous system that includes the medulla, the pons and the midbrain. The brain stem is a continuation of the spinal cord upward and forward (ventrally). It is in this region where most of the cranial nerves make their exits and entrances. There are 12 pairs of cranial nerves; Table 1 describes the name and main function of each pair and Figure 6 shows the entrance and exits of some cranial nerves in the brain.

                                                  Figure 6.  The brain shown from below with the entrance and exits of many cranial nerves.

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                                                  The Autonomic Nervous System

                                                  The autonomic nervous system is that part of the nervous system controlling the activity of the visceral components of the human body. It is called “autonomic” because it performs its functions automatically, meaning that its functioning cannot be easily controlled at will. From an anatomical point of view, the autonomic system has two main components: the sympathetic and the parasympathetic nervous system. The sympathetic nerves controlling visceral activity arise from the thoracic and lumbar portions of the spinal cord; parasympathetic nerves arise from the brain stem and the sacral portion of the spinal cord.

                                                  From a physiological point of view, no single generalization can be made that applies to the manner in which the sympathetic and the parasympathetic nervous systems control different body organs. In most cases, visceral organs are innervated by both systems, and each type has an opposite effect in a system of checks and balances. The heart, for example, is innervated by sympathetic nerves whose excitation produces an acceleration of the heartbeat, and by parasympathetic nerves whose excitation produce a slowing of the heartbeat. Either system can stimulate or inhibit the organs it innervates. In other cases, organs are predominantly or exclusively controlled by one system or the other. A vital function of the autonomic nervous system is the maintenance of homeostasis (stable state of equilibrium) and for the adaptation of the animal body to its external environment. Homeostasis is the state of equilibrium of body functions achieved by an active process; the control of body temperature, water and electrolytes are all examples of homeostatic processes.

                                                  From the pharmacological point of view, there is no single neurotransmitter associated with either sympathetic or parasympathetic functions, as was once believed. The old view that acetylcholine was the predominant transmitter of the autonomic system had to be abandoned when new classes of neurotransmitters and neuromodulators were found (e.g., dopamine, serotonin, purines and various neuropeptides).

                                                  Neuroscientists have recently revived the behavioural point of view of the autonomic nervous system. The autonomic nervous system is involved in the fight-or-flight instinctive reaction still present in humans, which is, for the most part, the basis for the physiological reactions caused by stress. Interactions between the nervous system and immunological functions are possible through the autonomic nervous system. Emotions that originate from the autonomic nervous system can be expressed via the skeletal muscles.

                                                  The autonomic control of smooth muscles

                                                  The muscles of the viscera—except for the heart—are the smooth muscles. Heart muscle has characteristics of both skeletal and smooth muscle. Like skeletal muscles, smooth muscles also contain the two proteins actin and, in smaller proportions, myosin. Unlike skeletal muscles, they do not present the regular organization of sarcolemes, the contractile unit of the muscle fibre. The heart is unique in that it can generate myogenic activity—even after its neural innervations have been severed, it can contract and relax for several hours by itself.

                                                  The neuromuscular coupling in smooth muscles differs from that of skeletal muscles. In skeletal muscles, the neuromuscular junction is the link between the nerve and the muscle fibres. In smooth muscle, there is no neuromuscular junction; the nerve endings enter the muscle, spreading in all directions. Electrical events inside the smooth muscle therefore are much slower than those in skeletal muscles. Finally, smooth muscle has the unique characteristic of exhibiting spontaneous contractions, such as that exhibited by the gut. To a large extent, the autonomic nervous system regulates the smooth muscles’ spontaneous activity.

                                                  The central components of the autonomic nervous system

                                                  The main role of the autonomic nervous system is to regulate the activity of smooth muscles, heart, glands in the digestive tract, sweat glands, and adrenal and other endocrine glands. The autonomic nervous system has a central component—the hypothalamus, located at the base of the brain—where many autonomic functions are integrated. Most importantly, the central components of the autonomic system are directly involved in the regulation of biological drives (temperature regulation, hunger, thirst, sex, urination, defecation and so on), motivation, emotion and to a great extent in “psychological” functions such as moods, affect and feelings.

                                                  Neuroendocrine System

                                                  Glands are the organs of the endocrine system. They are called endocrine glands because their chemical messages are delivered inside the body, directly into the blood stream (in contrast with exocrine glands, such as sweat glands, whose secretions appear on the outer surface of the body). The endocrine system provides slow but long-lasting control over organs and tissues through chemical messengers called hormones. Hormones are the main regulators of body metabolism. But, because of intimate links among the central, peripheral, and autonomic nervous systems, the neuroendocrine system—a term that captures such complex links—is now conceived of as a powerful modifier of the structure and function of the human body and behaviour.

                                                  Hormones have been defined as chemical messengers which are released from cells into the bloodstream to exert their action on target cells some distance away. Until recently, hormones were distinguished from neurotransmitters, discussed above. The latter are chemical messengers released from neurons onto a synapse between the nerve terminals and another neuron or an effector (i.e., muscle or gland). However, with the discovery that classical neurotransmitters such as dopamine can also act as hormones, the distinction between neurotransmitters and hormones is now less and less clear. Thus, based on purely anatomical considerations, hormones derived from nerve cells may be called neurohormones. From a functional point of view, the nervous system can be thought of as a truly neurosecretory system.

                                                  The hypothalamus controls endocrine functions through a link with the pituitary gland (also called the hypophysis, a tiny gland located at the base of the brain). Until the middle 1950s the endocrine glands were viewed as a separate system governed by the pituitary gland, often called the “master gland”. At that time, a neurovascular hypothesis was advanced that established the functional role of the hypothalamic/hypophysial factors in the control of endocrine function. In this view, the endocrine hypothalamus provides the final common neuroendocrine pathway in the control of the endocrine system. It has now been firmly established that the endocrine system is itself regulated by the central nervous system as well as the endocrine inputs. Thus, neuroendocrinology is now an appropriate term to describe the discipline that studies the reciprocal integrated roles of the nervous and the endocrine systems in the control of physiological processes.

                                                  With increasing understanding of neuroendocrinology, original divisions are breaking down. The hypothalamus, which is located above and connected to the pituitary gland, is the link between the nervous and the endocrine systems, and many of its nerve cells perform secretory functions. It is also linked with other major regions of the brain, including the rhinencephalon—the primitive cortex originally associated with olfaction or sense of smell—and the limbic system, associated with emotions. It is in the hypothalamus that hormones released by the posterior pituitary gland are produced. The hypothalamus also produces substances that are called releasing and inhibiting hormones. These act on the adenohypophysis, causing it to enhance or inhibit the production of anterior pituitary gland hormones, which act on glands located elsewhere (thyroid, adrenal cortex, ovaries, testicles and others).

                                                   

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                                                  Thursday, 17 February 2011 21:55

                                                  Nervous System: Overview

                                                  Knowledge of the nervous system in general and of the brain and human behaviour in particular are of paramount importance to those who are dedicated to a safe and healthy environment. Work conditions, and exposures that directly affect the operations of the brain, influence the mind and behaviour. To evaluate information, to make decisions and to react in a consistent and reasonable manner to perceptions of the world require that the nervous system functions properly and that behaviour not be damaged by dangerous conditions, such as accidents (e.g., a fall from a poorly designed ladder) or exposure to hazardous levels of neurotoxic chemicals.

                                                  Damage to the nervous system can cause changes in sensory input (loss of vision, hearing, smell, etc.), can hinder the capacity to control movement and body functions and/or can affect the brain’s capacity to treat or store information. In addition, altered nervous system functioning can cause behavioural or psychological disorders. Mood and personality changes are a common occurrence following physical or organic damage to the brain. As our knowledge develops, we are learning more about the way in which nervous system processes are modified. Neurotoxic substances can cross the brain’s natural barrier and directly interfere with its intricate workings. Although some substances have a particular affinity to certain areas of the nervous system, most neurotoxins have widespread effects, targeting cell processes involved in membrane transport, internal cellular chemical reactions, liberation of secretory substances, and so on.

                                                  Damage to the various components of the nervous system can occur in different ways:

                                                  • direct physical injury from falling objects, collisions, blows or undue pressure on nerves
                                                  • changes in the internal environment, such as insufficient oxygen due to asphyxiants and heat exposure
                                                  • interference in the cellular processes through chemical action by substances, such as metals, organic solvents and pesticides

                                                   

                                                  The insidious and multifaceted development of many nervous system disorders requires persons working in the field of occupational health to adopt different but complementary approaches to the study, understanding, prevention and treatment of the problem. Early alterations can be detected in groups of active, exposed workers using sensitive measures of impairment. Identification of initial dysfunction can lead to preventive actions. In the latter stages, a good clinical knowledge is required and differential diagnosis is essential to the adequate treatment and care of disabled workers.

                                                  Although chemical substances are mostly examined one by one, it should be remembered that in many workplaces mixtures of potentially neurotoxic chemicals are used, exposing workers to what can be called a “cocktail”. In processes such as printing, painting, cleaning, in poorly ventilated offices, in laboratories, pesticide application, microelectronics and many other sectors, workers are exposed to chemical mixtures. Although there may be information on each one of the substances separately, we have to consider the combined nocivity and possible additive or even synergistic effects on the nervous system. In some cases of multiple exposure, each particular chemical may be present in very small quantity, even below the detection level of exposure assessment techniques; however, when all are added together, the total concentration can be very high.

                                                  The reader should be aware of three major difficulties in reviewing facts about the nervous system within the scope of this Encyclopaedia.

                                                  First, the understanding of occupational diseases affecting the nervous system and behaviour has changed substantially as new approaches to viewing brain-behavioural relationships have developed. The main interest of characterization of gross morphological changes that occur due to mechanical trauma to the nervous system—particularly, but not exclusively to the brain—was followed by an interest in the absorption of neurotoxic agents by the nervous system; interest in the study of cellular mechanisms of nervous system pathology; and finally, the search for the molecular basis of these pathologic processes began to grow. These approaches coexist today and all contribute information for evaluating the working conditions affecting the brain, mind, and behaviour.

                                                  Second, the information generated by neuroscientists is staggering. The third edition of the book Principles of Neural Sciences edited by Kandel, Schwartz and Kessell which appeared in 1991—one of the most valuable reviews of the field—weighs 3.5 kg and is more than 1,000 pages long.

                                                  Third, it is very difficult to review knowledge about the functional organization of the nervous system as it applies to all niches of occupational health and safety. Until about 25 years ago, the theoretical views that gave support to those concerned health experts who specialize in the detection, monitoring, prevention, and the clinical treatment of a worker who has absorbed a neurotoxic agent sometimes did not overlap with theoretical views regarding workers’ brain trauma and the behavioural manifestations of minimal brain damage. Behavioural manifestations said to be the consequence of the disruption of specific chemical pathways in the brain were the exclusive territory of the neurotoxicologist; both structural tissue damage of specific regions of the brain, and distant neural structures linked to the area where the lesions occurred, were explanations invoked by neurologists. It is only in the past few years that converging views are appearing.

                                                  With this in mind, this chapter addresses issues important to the understanding of the nervous system and the effects of workplace conditions on its functioning. It begins with a description of the anatomy and physiology, followed by a section on neurotoxicity, which reviews exposure, outcomes and prevention.

                                                  Since the nervous system is central to the body’s well-being, many non-chemical hazards can likewise affect its normal functioning. Many of these are considered in different chapters dealing with these hazards. Traumatic head injuries are included in First Aid, heat stress is considered in the article “Effects of heat stress and work in the heat”, and decompression sickness is reviewed in the article “Gravitational stress”. Hand-arm vibration (“Hand-transmitted vibration”) and repetitive movement (“Chronic outcomes, musculoskeletal”) in the chapter Musculoskeletal System, which are risk factors for peripheral neuropathies, are likewise considered in these sections of the Encyclopaedia.

                                                  The chapter ends with a review of special issues and the outlook for future research avenues.

                                                   

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                                                  Thursday, 17 February 2011 00:15

                                                  General Lighting Conditions

                                                  Lighting is provided within interiors in order to satisfy the following requirements:

                                                  • to assist in providing a safe working environment
                                                  • to assist in the performance of visual tasks
                                                  • to develop an appropriate visual environment.

                                                   

                                                  The provision of a safe working environment has to be at the top of the list of priorities, and, in general, safety is increased by making hazards clearly visible. The order of priority of the other two requirements will depend to a large extent upon the use to which the interior is put. Task performance can be improved by ensuring that task detail is easier to see, while appropriate visual environments are developed by varying the lighting emphasis given to objects and surfaces within an interior.

                                                  Our general feeling of well-being, including morale and fatigue, is influenced by light and colour. Under low lighting levels, objects would have little or no colour or shape and there would be a loss in perspective. Conversely an excess of light may be just as unwanted as too little light.

                                                  In general, people prefer a room with daylight to a room which is windowless. Furthermore, contact with the outside world is considered to aid the feeling of well-being. The introduction of automatic lighting controls, together with high-frequency dimming of fluorescent lamps, has made it possible to provide interiors with a controlled combination of daylight and artificial light. This has the added benefit of saving on energy costs.

                                                  Perception of the character of an interior is influenced by both the brightness and colour of visible surfaces, both interior and exterior. The general lighting conditions within an interior can be achieved by using daylight or artificial lighting, or more likely by a combination of both.

                                                  Evaluation of Lighting

                                                  General requirements

                                                  Lighting systems used in commercial interiors can be sub-divided into three major categories—general lighting, localized lighting and local lighting.

                                                  General lighting installations typically provide an approximately uniform illuminance over the whole of the working plane. Such systems are often based upon the lumen method of design, where an average illuminance is:

                                                  Average illuminance (lux) =

                                                  Localized lighting systems provide illuminance on general work areas with a simultaneous reduced level of illuminance in adjacent areas.

                                                  Local lighting systems provide illuminance for relatively small areas incorporating visual tasks. Such systems are normally complemented by a specified level of general lighting. Figure 1 illustrates the typical differences between the systems described.

                                                  Figure 1. Lighting systems

                                                  LIG030F1

                                                  Where visual tasks are to be performed it is essential to achieve a demanded level of illuminance and to consider the circumstances that influence its quality.

                                                  The use of daylight to illuminate tasks has both merits and limitations. Windows admitting daylight into an interior provide good three-dimensional modelling, and though the spectral distribution of daylight varies throughout the day, its colour rendering is generally considered to be excellent.

                                                  However, a constant illuminance on a task cannot be provided by natural daylight only, due to its wide variability, and if the task is within the same field of view as a bright sky, then disabling glare is likely to occur, thereby impairing task performance. The use of daylight for task illuminance has only partial success, and artificial lighting, over which greater control can be exercised, has a major role to play.

                                                  Since the human eye will perceive surfaces and objects only through light which is reflected from them, it follows that surface characteristics and reflectance values together with the quantity and quality of light will influence the appearance of the                                                                                                                                       environment.

                                                  When considering the lighting of an interior it is essential to determine the illuminance level and to compare it with recommended levels for different tasks (see table 1).

                                                  Table 1. Typical recommended levels of maintained illuminance for different locations or visual tasks


                                                  Location/Task

                                                  Typical recommended level of maintained illuminance (lux)

                                                  General offices

                                                  500

                                                  Computer workstations

                                                  500

                                                  Factory assembly areas

                                                   

                                                  Rough work

                                                  300

                                                  Medium work

                                                  500

                                                  Fine work

                                                  750

                                                  Very fine work

                                                   

                                                  Instrument assembly

                                                  1,000

                                                  Jewellery assembly/repairs

                                                  1,500

                                                  Hospital operating theatres

                                                  50,000

                                                   

                                                  Lighting for visual tasks

                                                  The ability of the eye to discern detail—visual acuity—is significantly influenced by task size, contrast and the viewer’s visual performance. Increase in the quantity and quality of lighting will also significantly improve visual performance. The effect of lighting on task performance is influenced by the size of the critical details of the task and upon the contrast between task and surrounding background. Figure 2 shows the effects of illuminance upon visual acuity. When considering visual task lighting it is important to consider the ability of the eye to carry out the visual task with both speed and accuracy. This combination is known as visual performance. Figure 3 gives typical effects of illuminance on the visual performance of a given task.

                                                  Figure 2. Typical relationship between visual acuity and illuminance

                                                  LIG030F2

                                                  Figure 3. Typical relationship between visual performance and illuminance

                                                  LIG030F3

                                                  The prediction of illuminance reaching a working surface is of prime importance in lighting design. However, the human visual system responds to the distribution of luminance within the field of view. The scene within a visual field is interpreted by differentiating between surface colour, reflectance and illumination. Luminance depends upon both the illuminance on, and reflectance of, a surface. Both illuminance and luminance are objective quantities. The response to brightness, however, is subjective.

                                                   

                                                   

                                                   

                                                   

                                                  In order to produce an environment which provides visual satisfaction, comfort and performance, luminances within the field of view need to be balanced. Ideally the luminances surrounding a task should decrease gradually, thereby avoiding harsh contrasts. Suggested variation in luminance across a task is shown in figure 4.

                                                  Figure 4. Variation in luminance across a task

                                                  LIG030F4

                                                  The lumen method of lighting design leads to an average horizontal plane illuminance on the working plane, and it is possible to use the method to establish average illuminance values on the walls and ceilings within an interior. It is possible to convert average illuminance values into average luminance values from details of the mean reflectance value of the room surfaces.

                                                   

                                                   

                                                   

                                                  The equation relating luminance and illuminance is: 

                                                  Figure 5. Typical relative illuminance values together with suggested reflectance values

                                                  LIG030F5

                                                  Figure 5 shows a typical office with relative illuminance values (from an overhead general lighting system) on the main room surfaces together with suggested reflectances. The human eye tends to be drawn to that part of the visual scene which is brightest. It follows that higher luminance values usually occur at a visual task area. The eye acknowledges detail within a visual task by discriminating between lighter and darker parts of the task. The variation in brightness of a visual task is determined from calculation of the luminance contrast:

                                                  where

                                                  Lt = Luminance of the task

                                                  Lb = Luminance of the background

                                                  and both luminances are measured in cd·m–2

                                                  The vertical lines in this equation signify that all values of luminance contrast are to be considered positive.

                                                  The contrast of a visual task will be influenced by the reflectance properties of the task itself. See figure 5.

                                                  Optical Control of Lighting

                                                  If a bare lamp is used in a luminaire, the distribution of light is unlikely to be acceptable and the system will almost certainly be uneconomical. In such situations the bare lamp is likely to be a source of glare to the room occupants, and while some light may eventually reach the working plane, the effectiveness of the installation is likely to be seriously reduced because of the glare.

                                                  It will be evident that some form of light control is required, and the methods most frequently employed are detailed below.

                                                  Obstruction

                                                  If a lamp is installed within an opaque enclosure with only a single aperture for the light to escape, then the light distribution will be very limited, as shown in figure 6.

                                                  Figure 6. Lighting output control by obstruction

                                                  LIG030F6

                                                  Reflection

                                                  This method uses reflective surfaces, which may vary from a highly matt finish to a highly specular or mirror-like finish. This method of control is more efficient than obstruction, since stray light is collected and redirected to where it is required. The principle involved is shown in figure 7.

                                                  Figure 7. Light output control by reflection

                                                  LIG030F7

                                                  Diffusion

                                                  If a lamp is installed within a translucent material, the apparent size of the light source is increased with a simultaneous reduction in its brightness. Practical diffusers unfortunately absorb some of the emitted light, which consequently reduces the overall efficiency of the luminaire. Figure 8 illustrates the principle of diffusion.

                                                  Figure 8. Light output control by diffusion

                                                  LIG030F8

                                                  Refraction

                                                  This method uses the “prism” effect, where typically a prism material of glass or plastic “bends” the rays of light and in so doing redirects the light to where it is required. This method is extremely suitable for general interior lighting. It has the advantage of combining good glare control with an acceptable efficiency. Figure 9 shows how refraction assists in optical control.

                                                  In many cases a luminaire will use a combination of the methods of optical control described.

                                                  Figure 9. Light output control by refraction

                                                  LIG030F9

                                                  Luminance distribution

                                                  The light output distribution from a luminaire is significant in determining the visual conditions subsequently experienced. Each of the four methods of optical control described will produce differing light output distribution properties from the luminaire.

                                                  Veiling reflections often occur in areas where VDUs are installed. The usual symptoms experienced in such situations are reduced ability to read correctly from the text on a screen due to the appearance of unwanted high-luminance images on the screen itself, typically from overhead luminaires. A situation can develop where veiling reflections also appear on paper on a desk in an interior.

                                                  If the luminaires in an interior have a strong vertically downward component of light output, then any paper on a desk beneath such a luminaire will reflect the light source into the eyes of an observer who is reading from or working on the paper. If the paper has a gloss finish, the situation is aggravated.

                                                  The solution to the problem is to arrange for the luminaires used to have a light output distribution which is predominantly at an angle to the downward vertical, so that following the basic laws of physics (angle of incidence = angle of reflection) the reflected glare will be minimized. Figure 10 shows a typical example of both the problem and the cure. The light output distribution from the luminaire used to overcome the problem is referred to as a batwing distribution.

                                                  Figure 10. Veiling reflections

                                                  LIG30F10

                                                  Light distribution from luminaires can also lead to direct glare, and in an attempt to overcome this problem, local lighting units should be installed outside the 45-degree “forbidden angle”, as shown in figure 11.

                                                  Figure 11. Diagrammatic representation of the forbidden angle

                                                  LIG30F11

                                                  Optimal Lighting Conditions for Visual Comfortand Performance

                                                  It is appropriate when investigating lighting conditions for visual comfort and performance to consider those factors affecting the ability to see detail. These can be sub-divided into two categories—characteristics of the observer and characteristics of the task.

                                                  Characteristics of the observer.

                                                  These include:

                                                  • sensitivity of the individual’s visual system to size, contrast, exposure time
                                                  • transient adaptation characteristics
                                                  • susceptibility to glare
                                                  • age
                                                  • motivational and psychological characteristics.

                                                   

                                                  Characteristics of the task.

                                                  These include:

                                                  • configuration of detail
                                                  • contrast of detail/background
                                                  • background luminance
                                                  • specularity of detail.

                                                   

                                                  With reference to particular tasks, the following questions need to be answered:

                                                  • Are the task details easy to see?
                                                  • Is the task likely to be undertaken for lengthy periods?
                                                  • If errors result from the performance of the task, are the consequences considered to be serious?

                                                   

                                                  In order to produce optimal workplace lighting conditions it is important to consider the requirements placed upon the lighting installation. Ideally task lighting should reveal colour, size, relief and surface qualities of a task while simultaneously avoiding the creation of potentially dangerous shadows, glare and “harsh” surroundings to the task itself.

                                                  Glare.

                                                  Glare occurs when there is excessive luminance in the field of view. The effects of glare on vision can be divided into two groups, termed disability glare and discomfort glare.

                                                  Consider the example of glare from the headlights of an oncoming vehicle during darkness. The eye cannot adapt simultaneously to the headlights of the vehicle and to the much lower brightness of the road. This is an example of disability glare, since the high luminance light sources produce a disabling effect due to the scattering of light in the optic media. Disability glare is proportional to the intensity of the offending source of light.

                                                  Discomfort glare, which is more likely to occur in interiors, can be reduced or even totally eliminated by reducing the contrast between the task and its surroundings. Matt, diffusely reflecting finishes on work surfaces are to be preferred to gloss or specularly reflecting finishes, and the position of any offending light source should be outside the normal field of vision. In general, successful visual performance occurs when the task itself is brighter than its immediate surrounds, but not excessively.

                                                  The magnitude of discomfort glare is given a numerical value and compared with reference values in order to predict whether the level of discomfort glare will be acceptable. The method of calculation of glare index values used in the UK and elsewhere is considered under “Measurement”.

                                                  Measurement

                                                  Lighting surveys

                                                  One survey technique often used relies upon a grid of measuring points over the whole area under consideration. The basis of this technique is to divide the whole of the interior into a number of equal areas, each ideally square. The illuminance at the centre of each of the areas is measured at desk-top height (typically 0.85 metres above floor level), and an average value of illuminance is calculated. The accuracy of the value of average illuminance is influenced by the number of measuring points used.

                                                  A relationship exists which enables the minimum number of measuring points to be calculated from the value of room index applicable to the interior under consideration.

                                                  Here, length and width refer to the room dimensions, and mounting height is the vertical distance between the centre of the light source and the working plane.

                                                  The relationship referred to is given as:

                                                  Minimum number of measuring points = (x + 2)2

                                                  where “x” is the value of the room index taken to the next highest whole number, except that for all values of RI equal to or greater than 3, x is taken as 4. This equation gives the minimum number of measuring points, but conditions often require more than this minimum number of points to be used.

                                                  When considering the lighting of a task area and its immediate surround, variance in illuminance or uniformity of illuminance must be considered.

                                                  Over any task area and its immediate surround, uniformity should be not less than 0.8.

                                                  In many workplaces it is unnecessary to illuminate all areas to the same level. Localized or local lighting may provide some degree of energy saving, but whichever system is used the variance in illuminance across an interior must not be excessive.

                                                  The diversity of illuminance is expressed as:

                                                  At any point in the major area of the interior, the diversity of illuminance should not exceed 5:1.

                                                  Instruments used for measuring illuminance and luminance typically have spectral responses which vary from the response of the human visual system. The responses are corrected, often by the use of filters. When filters are incorporated, the instruments are referred to as colour corrected.

                                                  Illuminance meters have a further correction applied which compensates for the direction of incident light falling upon the detector cell. Instruments which are capable of accurately measuring illuminance from varying directions of incident light are said to be cosine corrected.

                                                  Measurement of glare index

                                                  The system used frequently in the UK, with variations elsewhere, is essentially a two-stage process. The first stage establishes an uncorrected glare index value (UGI). Figure 12 provides an example.

                                                  Figure 12. Elevation and plan views of typical interior used in example

                                                  LIG30F12

                                                  The height H is the vertical distance between the centre of the light source and the eye level of a seated observer, which is normally taken as 1.2 metres above floor level. The major dimensions of the room are then converted into multiples of H. Thus, since H = 3.0 metres, then length = 4H and width = 3H. Four separate calculations of UGI have to be made in order to determine the worst case scenario in accordance with the layouts shown in figure 13.

                                                  Figure 13. Possible combinations of luminaire orientation and viewing direction within the interior considered in the example

                                                  LIG30F13

                                                  Tables are produced by lighting equipment manufacturers which specify, for given values of fabric reflectance within a room, values of uncorrected glare index for each combination of values of X and Y.

                                                  The second stage of the process is to apply correction factors to the UGI values depending upon values of lamp output flux and deviation in value of height (H).

                                                  The final glare index value is then compared with the Limiting Glare Index value for specific interiors, given in references such as the CIBSE Code for Interior Lighting (1994).

                                                   

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