Arsenic toxicity and potential mechanisms of action

被引:1285
作者
Hughes, MF [1 ]
机构
[1] US EPA, Off Res & Dev, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
关键词
arsenic; toxicity; mechanisms;
D O I
10.1016/S0378-4274(02)00084-X
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Exposure to the metalloid arsenic is a daily occurrence because of its environmental pervasiveness. Arsenic, which is found in several different chemical forms and oxidation states, causes acute and chronic adverse health effects, including cancer. The metabolism of arsenic has an important role in its toxicity. The metabolism involves reduction to a trivalent state and oxidative methylation to a pentavalent state. The trivalent arsenicals, including those methylated, have more potent toxic properties than the pentavalent arsenicals. The exact mechanism of the action of arsenic is not known, but several hypotheses have been proposed. At a biochemical level, inorganic arsenic in the pentavalent state may replace phosphate in several reactions. In the trivalent state, inorganic and organic (methylated) arsenic may react with critical thiols in proteins and inhibit their activity. Regarding cancer, potential mechanisms include genotoxicity, altered DNA methylation, oxidative stress, altered cell proliferation, co-carcinogenesis, and tumor promotion. A better understanding of the mechanism(s) of action of arsenic will make a more confident determination of the risks associated with exposure to this chemical. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 16
页数:16
相关论文
共 136 条
[91]  
ROSSMAN TG, 1980, ENV MUTAGEN, V2, P307
[92]   Dietary garlic extract in modifying clastogenic effects of inorganic arsenic in mice: Two-generation studies [J].
RoyChoudhury, A ;
Das, T ;
Sharma, A ;
Talukder, G .
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, 1996, 359 (03) :165-170
[93]   NEOPLASTIC TRANSFORMATION OF BALB/3T3 CELLS BY METALS AND THE QUEST FOR INDUCTION OF A METASTATIC PHENOTYPE [J].
SAFFIOTTI, U ;
BERTOLERO, F .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1989, 21 :475-482
[94]  
SCHROEDER HAM, 1968, J NUTR, V6, P37
[95]   REACTIONS OF ARSENIC(III) AND ARSENIC(V) SPECIES WITH GLUTATHIONE [J].
SCOTT, N ;
HATLELID, KM ;
MACKENZIE, NE ;
CARTER, DE .
CHEMICAL RESEARCH IN TOXICOLOGY, 1993, 6 (01) :102-106
[96]   Lack of promoting effect due to oral administration of dimethylarsinic acid on rat lung carcinogenesis initiated with N-bis(2-hydroxypropyl)nitrosamine [J].
Seike, N ;
Wanibuchi, H ;
Morimura, K ;
Nishikawa, T ;
Kishida, H ;
Nakae, D ;
Hirata, K ;
Fukushima, S .
CANCER LETTERS, 2002, 175 (02) :113-119
[97]   CANCER RISKS FROM ARSENIC IN DRINKING-WATER [J].
SMITH, AH ;
HOPENHAYNRICH, C ;
BATES, MN ;
GOEDEN, HM ;
HERTZPICCIOTTO, I ;
DUGGAN, HM ;
WOOD, R ;
KOSNETT, MJ ;
SMITH, MT .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1992, 97 :259-267
[98]   Comparative in vitro methylation of trivalent and pentavalent arsenicals [J].
Styblo, M ;
Yamauchi, H ;
Thomas, DJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 135 (02) :172-178
[99]   Comparative inhibition of yeast glutathione reductase by arsenicals and arsenothiols [J].
Styblo, M ;
Serves, SV ;
Cullen, WR ;
Thomas, DJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (01) :27-33
[100]   Comparative toxicity of trivalent and pentavalent inorganic and methylated arsenicals in rat and human cells [J].
Styblo, M ;
Del Razo, LM ;
Vega, L ;
Germolec, DR ;
LeCluyse, EL ;
Hamilton, GA ;
Reed, W ;
Wang, C ;
Cullen, WR ;
Thomas, DJ .
ARCHIVES OF TOXICOLOGY, 2000, 74 (06) :289-299