Genetic factors in neurotoxicology and neuropharmacology: A critical evaluation of the use of genetics as a research tool
- 1 October 1991
- journal article
- review article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 47 (10), 990-998
- https://doi.org/10.1007/bf01923334
Abstract
Animals have evolved a detoxication system to enable them to survive in a hostile chemical environment in which foods contain many non-nutrient chemicals. Detoxication depends on enzymes which are often genetically polymorphic. As a result, inter-individual variation is common, and in humans several Mendelian loci have been identified. However, most variation in response is probably due to the action of several genes. Genetic variation in response to the neurotoxin MPTP and to chemically and physically-induced seizures is reviewed. In the former case, differences between pigmented and white mouse strains have been noted which are consistent with the hypothesis that humans are more sensitive than mice or rats because of the presence of melanin in human brains. However, variation in sensitivity probably also depends on other genes. In the case of audiogenic seizures, a single locus has been identified and mapped, but its relationship with seizures induced by other agents is not clear. Genetic variation in response to alcohol is also discussed. The failure of most toxicologists to consider genetic variation as a potentially confounding variable, and as a powerful research tool, is discussed critically in relation to non-repeatability of research on the neurotoxic effects of lead, and in relation to the genetic variation in MPTP, seizures, and alcohol response already noted. It seems clear that genetic methods provide a powerful research tool which is largely being ignored by toxicologists.Keywords
This publication has 66 references indexed in Scilit:
- 5-HT2 receptor binding and 5-HT uptake in mouse brain: developmental changes and the relationship to audiogenic seizure susceptibility in DBA/2J miceDevelopmental Brain Research, 1989
- Strain differences in systematic 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity in mice correlate best with monoamine oxidase activity at the blood-brain barrierLife Sciences, 1988
- Mouse strain differences in operant self-administration of ethanolBehavior Genetics, 1987
- Comparative toxicity and biotransformation of lindane in C57BL/6 and DBA/2 miceLife Sciences, 1986
- Genetically Determined Variability in Acetylation and Oxidation Therapeutic ImplicationsDrugs, 1985
- Further investigation of racial/ethnic differences and of familial resemblances in flushing in response to alcoholBehavior Genetics, 1984
- A simplified triple-test cross analysis of alcohol preference in the ratBehavior Genetics, 1981
- Genetic analysis of tolerance to ethanol hypothermia in recombinant inbred mice: Effect of desglycinamide(9)-Arginine(8)-vasopressinBehavior Genetics, 1980
- Behavior in chimeric mice combining differently behaving strainsBehavior Genetics, 1979
- Ethanol-induced hypothermia in mice: Influence of genotype on development of toleranceLife Sciences, 1978