Arsenic Exposure and Toxicology: A Historical Perspective

被引:933
作者
Hughes, Michael F. [1 ]
Beck, Barbara D. [3 ]
Chen, Yu [2 ]
Lewis, Ari S. [3 ]
Thomas, David J. [1 ]
机构
[1] US EPA, Off Res & Dev, Natl Hlth & Environm Effects Res Lab, Res Triangle Pk, NC 27711 USA
[2] NYU, Dept Environm Med, Sch Med, New York, NY 10016 USA
[3] Gradient Corp, Cambridge, MA 02138 USA
关键词
arsenic; cancer; exposure; INDUCED MALIGNANT-TRANSFORMATION; CHILDRENS INTELLECTUAL FUNCTION; TRANSITIONAL-CELL CARCINOMA; PREMALIGNANT SKIN-LESIONS; LUNG-CANCER MORTALITY; DNA-STRAND BREAKS; DRINKING-WATER; DIMETHYLARSINIC ACID; MONOMETHYLARSONOUS ACID; SODIUM ARSENITE;
D O I
10.1093/toxsci/kfr184
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The metalloid arsenic is a natural environmental contaminant to which humans are routinely exposed in food, water, air, and soil. Arsenic has a long history of use as a homicidal agent, but in the past 100 years arsenic, has been used as a pesticide, a chemotherapeutic agent and a constituent of consumer products. In some areas of the world, high levels of arsenic are naturally present in drinking water and are a toxicological concern. There are several structural forms and oxidation states of arsenic because it forms alloys with metals and covalent bonds with hydrogen, oxygen, carbon, and other elements. Environmentally relevant forms of arsenic are inorganic and organic existing in the trivalent or pentavalent state. Metabolism of arsenic, catalyzed by arsenic (+3 oxidation state) methyltransferase, is a sequential process of reduction from pentavalency to trivalency followed by oxidative methylation back to pentavalency. Trivalent arsenic is generally more toxicologically potent than pentavalent arsenic. Acute effects of arsenic range from gastrointestinal distress to death. Depending on the dose, chronic arsenic exposure may affect several major organ systems. A major concern of ingested arsenic is cancer, primarily of skin, bladder, and lung. The mode of action of arsenic for its disease endpoints is currently under study. Two key areas are the interaction of trivalent arsenicals with sulfur in proteins and the ability of arsenic to generate oxidative stress. With advances in technology and the recent development of animal models for arsenic carcinogenicity, understanding of the toxicology of arsenic will continue to improve.
引用
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页码:305 / 332
页数:28
相关论文
共 328 条
[71]  
DOUDOROFF M, 1947, J BIOL CHEM, V170, P147
[72]   Metabolism and toxicity of arsenic in human urothelial cells expressing rat arsenic (+3 oxidation state)-methyltransferase [J].
Drobná, Z ;
Waters, SB ;
Devesa, V ;
Harmon, AW ;
Thomas, DJ ;
Styblo, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 207 (02) :147-159
[73]   Interindividual variation in the metabolism of arsenic in cultured primary human hepatocytes [J].
Drobná, Z ;
Waters, SB ;
Walton, FS ;
LeCluyse, EL ;
Thomas, DJ ;
Styblo, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 201 (02) :166-177
[74]   shRNA silencing of AS3MT expression minimizes arsenic methylation capacity of HepG2 cells [J].
Drobna, Zuzana ;
Xing, Weibing ;
Thomas, David J. ;
Styblo, Miroslav .
CHEMICAL RESEARCH IN TOXICOLOGY, 2006, 19 (07) :894-898
[75]   Disruption of the Arsenic (+3 Oxidation State) Methyltransferase Gene in the Mouse Alters the Phenotype for Methylation of Arsenic and Affects Distribution and Retention of Orally Administered Arsenate [J].
Drobna, Zuzana ;
Naranmandura, Hua ;
Kubachka, Kevin M. ;
Edwards, Brenda C. ;
Herbin-Davis, Karen ;
Styblo, Miroslav ;
Chris Le, X. ;
Creed, John T. ;
Maeda, Noboyu ;
Hughes, Michael F. ;
Thomas, David J. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2009, 22 (10) :1713-1720
[76]   Influence of arsenate and arsenite on signal transduction pathways: an update [J].
Druwe, Ingrid L. ;
Vaillancourt, Richard R. .
ARCHIVES OF TOXICOLOGY, 2010, 84 (08) :585-596
[77]  
Dunlap LG, 1921, J AMER MED ASSOC, V76, P568
[78]   Development of a human physiologically based pharmacokinetic (PBPK) model for inorganic arsenic and its mono- and di-methylated metabolites [J].
El-Masri, Hisham A. ;
Kenyon, Elaina M. .
JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2008, 35 (01) :31-68
[79]  
ENDO G, 1992, B ENVIRON CONTAM TOX, V48, P131
[80]   CANCERS RELATED TO EXPOSURE TO ARSENIC AT A COPPER SMELTER [J].
ENTERLINE, PE ;
DAY, R ;
MARSH, GM .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 1995, 52 (01) :28-32