Target Organ Metabolism, Toxicity, and Mechanisms of Trichloroethylene and Perchloroethylene: Key Similarities, Differences, and Data Gaps

被引:56
作者
Cichocki, Joseph A. [1 ]
Guyton, Kathryn Z. [2 ]
Guha, Neela [2 ]
Chiu, Weihsueh A. [1 ]
Rusyn, Ivan [1 ]
Lash, Lawrence H. [3 ]
机构
[1] Texas A&M Univ, Coll Vet Med & Biomed Sci, Dept Vet Integrat Biosci, College Stn, TX USA
[2] Int Agcy Res Canc, Lyon, France
[3] Wayne State Univ, Sch Med, Dept Pharmacol, 540 East Canfield Ave, Detroit, MI 48201 USA
基金
美国国家卫生研究院;
关键词
RENAL-CELL CARCINOMA; PHARMACOKINETIC PBPK MODEL; SISTER-CHROMATID EXCHANGES; NERVE-CONDUCTION VELOCITY; UNSCHEDULED DNA-SYNTHESIS; TISSUE-SPECIFIC TOXICITY; LYASE-MEDIATED CLEAVAGE; LIVER-TUMOR-INDUCTION; CONJUGATE BETA-LYASE; NON-HODGKIN-LYMPHOMA;
D O I
10.1124/jpet.116.232629
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Trichloroethylene (TCE) and perchloroethylene or tetrachloroethylene (PCE) are high-production volume chemicals with numerous industrial applications. As a consequence of their widespread use, these chemicals are ubiquitous environmental contaminants to which the general population is commonly exposed. It is widely assumed that TCE and PCE are toxicologically similar; both are simple olefins with three (TCE) or four (PCE) chlorines. Nonetheless, despite decades of research on the adverse health effects of TCE or PCE, few studies have directly compared these two toxicants. Although the metabolic pathways are qualitatively similar, quantitative differences in the flux and yield of metabolites exist. Recent human health assessments have uncovered some overlap in target organs that are affected by exposure to TCE or PCE, and divergent species and sex-specificity with regard to cancer and noncancer hazards. The objective of this minireview is to highlight key similarities, differences, and data gaps in target organ metabolism and mechanism of toxicity. The main anticipated outcome of this review is to encourage research to 1) directly compare the responses to TCE and PCE using more sensitive biochemical techniques and robust statistical comparisons; 2) more closely examine interindividual variability in the relationship between toxicokinetics and toxicodynamics for TCE and PCE; 3) elucidate the effect of coexposure to these two toxicants; and 4) explore new mechanisms for target organ toxicity associated with TCE and/or PCE exposure.
引用
收藏
页码:110 / 123
页数:14
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