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毛蕊花糖苷对四氯化碳诱导的肝毒性的保护作用。

Protective effect of acteoside on carbon tetrachloride-induced hepatotoxicity.

作者信息

Lee Kyung Jin, Woo Eun-Rhan, Choi Chul Yung, Shin Dong Weon, Lee Dong Gun, You Ho Jin, Jeong Hye Gwang

机构信息

Department of Pharmacy, College of Pharmacy, Research Center for Proteineous Materials, Chosun University, 375 Seosuk-dong, Kwangju 501-759, South Korea.

出版信息

Life Sci. 2004 Jan 9;74(8):1051-64. doi: 10.1016/j.lfs.2003.07.020.

Abstract

This study investigated the protective effects of acteoside, a phenylethanoid glycoside, on the carbon tetrachloride-induced hepatotoxicity as well as the possible mechanisms involved in this protection in mice. Pretreatment with acteoside prior to the administration of carbon tetrachloride significantly prevented the increased serum enzymatic activities of alanine and aspartate aminotransferase in a dose-dependent manner. In addition, pretreatment with acteoside significantly prevented the increase in hepatic malondialdehyde formation and the depletion of the reduced glutathione content in the liver of carbon tetrachloride-intoxicated mice. Carbon tetrachloride-induced hepatotoxicity was also essentially prevented, as indicated by a liver histopathologic study. The effects of acteoside on cytochrome P450 (P450) 2E1, the major isozyme involved in carbon tetrachloride bioactivation were also investigated. Treatment of the mice with acteoside resulted in a significant decrease in the P450 2E1-dependent pnitrophenol and aniline hydroxylation in a dose-dependent manner. Consistent with these observations, the P450 2El protein levels were also lower. Acteoside exhibited anti-oxidant effects on FeCl2-ascorbate induced lipid peroxidation in a mouse liver homogenate, and on superoxide radical scavenging activity. These results suggest that the protective effects of acteoside against the carbon tetrachloride-induced hepatotoxicity possibly involve mechanisms related to its ability to block the P450-mediated carbon tetrachloride bioactivation and free radical scavenging effects.

摘要

本研究调查了苯乙醇苷类化合物毛蕊花糖苷对四氯化碳诱导的小鼠肝毒性的保护作用及其可能的保护机制。在给予四氯化碳之前用毛蕊花糖苷预处理,可显著预防血清中丙氨酸氨基转移酶和天冬氨酸氨基转移酶活性的升高,且呈剂量依赖性。此外,用毛蕊花糖苷预处理可显著预防四氯化碳中毒小鼠肝脏中丙二醛生成的增加以及还原型谷胱甘肽含量的减少。肝脏组织病理学研究表明,四氯化碳诱导的肝毒性也基本得到预防。还研究了毛蕊花糖苷对细胞色素P450(P450)2E1的影响,P450 2E1是参与四氯化碳生物活化的主要同工酶。用毛蕊花糖苷处理小鼠后,P450 2E1依赖性对硝基苯酚和苯胺羟化反应显著降低,且呈剂量依赖性。与这些观察结果一致,P450 2E1蛋白水平也较低。毛蕊花糖苷对小鼠肝脏匀浆中FeCl2-抗坏血酸诱导的脂质过氧化以及超氧自由基清除活性具有抗氧化作用。这些结果表明,毛蕊花糖苷对四氯化碳诱导的肝毒性的保护作用可能涉及其阻断P450介导的四氯化碳生物活化的能力和自由基清除作用相关的机制。

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