a College of Pharmacy and Pharmaceutical Sciences , University of Toledo , Toledo , Ohio , USA.
J Toxicol Environ Health A. 2014;77(6):313-23. doi: 10.1080/15287394.2013.864576.
Dichloroacetate (DCA) and trichloroacetate (TCA) are drinking-water chlorination by-products previously found to induce oxidative stress (OS) in hepatic tissues of B6C3F1 male mice. To assess the effects of mixtures of the compounds on OS, groups of male B6C3F1 mice were treated daily by gavage with DCA at doses of 7.5, 15, or 30 mg/kg/d, TCA at doses of 12.5, 25, or 50 mg/kg/d, and 3 mixtures of DCA and TCA (Mix I, Mix II, and Mix III), for 13 wk. The concentrations of the compounds in Mix I, Mix II, and Mix III corresponded to those producing approximately 15, 25, and 35%, respectively, of maximal induction of OS by individual compounds. Livers were assayed for production of superoxide anion (SA), lipid peroxidation (LP), and DNA single-strand breaks (SSB). DCA, TCA, and the mixtures produced dose-dependent increases in the three tested biomarkers. Mix I and II effects on the three biomarkers, and Mix III effect on SA production were found to be additive, while Mix III effects on LP and DNA-SSB were shown to be greater than additive. Induction of OS in livers of B6C3F1 mice after subchronic exposure to DCA and TCA was previously suggested as an important mechanism in chronic hepatotoxicity/hepatocarcinogenicity induced by these compounds. Hence, there may be rise in exposure risk to these compounds as these agents coexist in drinking water.
二氯乙酸 (DCA) 和三氯乙酸 (TCA) 是饮用水氯化副产物,先前已发现其能诱导 B6C3F1 雄性小鼠肝组织发生氧化应激 (OS)。为评估这些化合物混合物对 OS 的影响,雄性 B6C3F1 小鼠经灌胃给予 DCA,剂量分别为 7.5、15 或 30 mg/kg/d,TCA 剂量分别为 12.5、25 或 50 mg/kg/d,以及 3 种 DCA 和 TCA 的混合物 (Mix I、Mix II 和 Mix III),每天处理 13 周。Mix I、Mix II 和 Mix III 中化合物的浓度分别对应于单独化合物引起 OS 最大诱导的约 15%、25%和 35%。测定肝脏中超氧阴离子 (SA)、脂质过氧化 (LP) 和 DNA 单链断裂 (SSB) 的产生。DCA、TCA 和混合物以剂量依赖的方式增加了三种测试生物标志物的产生。发现 Mix I 和 II 对三种生物标志物的影响,以及 Mix III 对 SA 产生的影响具有加性,而 Mix III 对 LP 和 DNA-SSB 的影响大于加性。先前有研究表明,B6C3F1 小鼠在亚慢性暴露于 DCA 和 TCA 后,肝 OS 的诱导是这些化合物引起慢性肝毒性/致癌性的重要机制。因此,这些化合物在饮用水中共存时,可能会增加暴露风险。