Protective effects of molecular hydrogen on hepatotoxicity induced by sub-chronic exposure to chlorpyrifos in rats.

Zhi-Ming Xun, Fei Xie, Peng-Xiang Zhao, Meng-Yu Liu, Zhi-Yuan Li, Jian-Mei Song, Xian-Min Kong, Xue-Mei Ma, Xiao-Yang Li
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引用次数: 3

Abstract

INTRODUCTION Chlorpyrifos (CPF) is a organophosphate insecticide widely used in agriculture with attendant adverse health outcomes. Chronic exposure to CPF induces oxidative stress and elicits harmful effects, including hepatic dysfunction. Molecular hydrogen has been identified as a novel antioxidant which could selectively scavenge hydroxyl radicals. OBJECTIVE The aim of this study was to determine whether the intake of hydrogen-rich water (HRW) could protect rats from hepatotoxicity caused by sub-chronic exposure to CPF. MATERIAL AND METHODS Rats were treated with hydrogen-rich water by oral intake for 8 weeks. Biochemical indicators of liver function, SOD and CAT activity, GSH and MDA levels were determined by the spectrophotometric method. Liver cell damage induced by CPF was evaluated by histopathological and electron microscopy analysis. PCR array analysis was performed to investigated the effects of molecular hydrogen on the regulation of oxidative stress related genes. RESULTS Both the hepatic function tests and histopathological analysis showed that the liver damage induced by CPF could be ameliorated by HRW intake. HRW intake also attenuated CPF induced oxidative stress, as evidenced by restored SOD activities and MDA levels. The results of PCR Array identified 12 oxidative stress-related genes differentially expressed after CPF exposure, 8 of chich, including the mitochondrial Sod2 gene, were significantly attenuated by HRW intake. The electron microscopy results indicated that the mitochondrial damage caused by CPF was alleviated after HRW treatment. CONCLUSIONS The results obtained suggest that HRW intake can protect rats from CPF induced hepatotoxicity, and the oxidative stress signaling and the mitochondrial pathway may be involved in the protection of molecular hydrogen.
分子氢对毒死蜱亚慢性暴露大鼠肝毒性的保护作用。
毒死蜱(Chlorpyrifos, CPF)是一种广泛应用于农业的有机磷杀虫剂,具有不良的健康后果。慢性暴露于CPF可诱导氧化应激并引起包括肝功能障碍在内的有害影响。氢分子是一种具有选择性清除羟基自由基的新型抗氧化剂。目的:探讨富氢水(HRW)对大鼠亚慢性CPF肝毒性的保护作用。材料与方法:大鼠口服富氢水8周。采用分光光度法测定肝功能生化指标、SOD、CAT活性、GSH、MDA水平。采用组织病理学和电镜观察观察CPF对肝细胞的损伤。采用PCR阵列分析研究氢分子对氧化应激相关基因的调控作用。结果:肝功能检查和组织病理学分析显示,摄入HRW可改善CPF所致的肝损伤。HRW摄入也可以减弱CPF诱导的氧化应激,这可以通过恢复SOD活性和MDA水平来证明。PCR阵列结果鉴定出CPF暴露后12个氧化应激相关基因的差异表达,其中包括线粒体Sod2基因在内的8个基因被HRW摄入显著减弱。电镜观察结果显示,HRW处理后CPF引起的线粒体损伤有所减轻。结论:HRW摄入对CPF所致大鼠肝毒性具有保护作用,分子氢的保护作用可能与氧化应激信号通路和线粒体通路有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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