Genetic polymorphism in the biotransformation of inorganic arsenic and its role in toxicity

被引:211
作者
Vahter, M [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, S-17177 Stockholm, Sweden
关键词
arsenic metabolism; variation; species; methyltransferases;
D O I
10.1016/S0378-4274(99)00271-4
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Arsenic is a recognized human carcinogen, but experimental cancer studies are negative. There is a variation in susceptibility among individuals, which probably is related to variation in metabolism. Inorganic arsenic is methylated to methylarsonic acid (MMA) and dimethylarsinic acid (DMA), which are less toxic and more readily excreted in urine than the inorganic arsenic. The rate of methylation of arsenic varies considerably between species. Most population groups studied so far have on average 10-30% inorganic, 10-20% MMA, and 60-70% DMA in urine, but there is a considerable inter-individual variation. Also, recent studies have identified groups with unusually low or high urinary excretion of MMA. Thus, there seems to be a genetic polymorphism in the biomethylation of arsenic. However, the methyltransferases involved in arsenic methylation have not been characterized. (C) 2000 Published by Elsevier Science Inland Ltd. All rights reserved.
引用
收藏
页码:209 / 217
页数:9
相关论文
共 60 条
[31]   THE EFFECT OF METHYLTRANSFERASE INHIBITION ON THE METABOLISM OF [AS-74] ARSENITE IN MICE AND RABBITS [J].
MARAFANTE, E ;
VAHTER, M .
CHEMICO-BIOLOGICAL INTERACTIONS, 1984, 50 (01) :49-57
[32]   Relative genotoxic potency of arsenic and its methylated metabolites [J].
Moore, MM ;
HarringtonBrock, K ;
Doerr, CL .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 1997, 386 (03) :279-290
[33]  
National Research Council, 1999, RISK ASS ARS DRINK W, P263
[34]   Induction of chromosomal aberrations in cultured human fibroblasts by inorganic and organic arsenic compounds and the different roles of glutathione in such induction [J].
OyaOhta, Y ;
Kaise, T ;
Ochi, T .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1996, 357 (1-2) :123-129
[35]   Variation in arsenic-induced sister chromatid exchange in human lymphocytes and lymphoblastoid cell lines [J].
Rasmussen, RE ;
Menzel, DB .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 1997, 386 (03) :299-306
[36]   Inorganic and methylated arsenic compounds induce cell death in murine macrophages via different mechanisms [J].
Sakurai, T ;
Kaise, T ;
Matsubara, C .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (04) :273-283
[37]   Mouse liver nicotinamide N-methyltransferase pharmacogenetics: Biochemical properties and variation in activity among inbred strains [J].
Scheller, T ;
Orgacka, H ;
Szumlanski, CL ;
Weinshilboum, RM .
PHARMACOGENETICS, 1996, 6 (01) :43-53
[38]   PHARMACOGENETICS OF N-METHYLATION - HERITABILITY OF HUMAN-ERYTHROCYTE HISTAMINE N-METHYLTRANSFERASE ACTIVITY [J].
SCOTT, MC ;
VANLOON, JA ;
WEINSHILBOUM, RM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1988, 43 (03) :256-262
[39]  
Stockler S, 1996, AM J HUM GENET, V58, P914
[40]   Metabolism of arsenic in primary cultures of human and rat hepatocytes [J].
Styblo, M ;
Del Razo, LM ;
LeCluyse, EL ;
Hamilton, GA ;
Wang, CQ ;
Cullen, WR ;
Thomas, DJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1999, 12 (07) :560-565