GENETIC-FACTORS IN NEUROTOXICOLOGY AND NEUROPHARMACOLOGY - A CRITICAL-EVALUATION OF THE USE OF GENETICS AS A RESEARCH TOOL

被引:13
作者
FESTING, MFW
机构
[1] MRC Toxicology Unit, Carshalton, SM5 4EF, Surrey, Woodmansterne Road
来源
EXPERIENTIA | 1991年 / 47卷 / 10期
关键词
PHARMACOGENETICS; NEUROTOXICOLOGY; TOXICOLOGY; NEUROPHARMACOLOGY; MPTP; SEIZURES; ALCOHOL; INBRED STRAINS; DETOXICATION;
D O I
10.1007/BF01923334
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:990 / 999
页数:10
相关论文
共 97 条
[1]  
ALBERT A, 1987, XENOBIOSIS
[2]  
Anderson R. M., 1988, Genetics of resistance to bacterial and parasitic infection., P233
[3]   GENETICS OF HISTOCOMPATIBILITY IN MICE .1. NEW LOCI AND CONGENIC LINES [J].
BAILEY, DW .
IMMUNOGENETICS, 1975, 2 (03) :249-256
[5]   GENES THAT AFFECT THE SHAPE OF THE MURINE MANDIBLE - CONGENIC STRAIN ANALYSIS [J].
BAILEY, DW .
JOURNAL OF HEREDITY, 1985, 76 (02) :107-114
[6]   DIFFERENTIAL NEUROSENSITIVITY TO 3 ALCOHOLS AND PHENOBARBITAL IN C57BL/6J AND DBA/2J MICE [J].
BELKNAP, JK ;
DEUTSCH, CK .
BEHAVIOR GENETICS, 1982, 12 (03) :309-317
[7]  
BLOOMQUIST JR, 1986, NEUROTOXICOLOGY, V7, P217
[8]   EVOLUTIONARY BIOLOGY, ANIMAL BEHAVIOR, 4TH-DIMENSIONAL SPACE, AND THE RAISON DETRE OF DRUG-METABOLISM AND PHARMACOKINETICS [J].
BOXENBAUM, H .
DRUG METABOLISM REVIEWS, 1983, 14 (05) :1057-1097
[9]   THE EFFECT OF 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE (MPTP) ON STRIATAL AND LIMBIC CATECHOLAMINE NEURONS IN WHITE AND BLACK MICE - ANTAGONISM BY MONOAMINE-OXIDASE INHIBITORS [J].
BRADBURY, AJ ;
COSTALL, B ;
JENNER, PG ;
KELLY, ME ;
MARSDEN, CD ;
NAYLOR, RJ .
NEUROPHARMACOLOGY, 1986, 25 (08) :897-904
[10]   A PRIMATE MODEL OF PARKINSONISM - SELECTIVE DESTRUCTION OF DOPAMINERGIC-NEURONS IN THE PARS COMPACTA OF THE SUBSTANTIA NIGRA BY N-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE [J].
BURNS, RS ;
CHIUEH, CC ;
MARKEY, SP ;
EBERT, MH ;
JACOBOWITZ, DM ;
KOPIN, IJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (14) :4546-4550