Oxidative stress mediates drug-induced hepatotoxicity in rats: a possible role of DNA fragmentation

被引：94

作者：

Amin, A ^{[1
]}

Hamza, AA ^{[1
]}

机构：

[1] UAE Univ Al Ain, Al Ain, U Arab Emirates

来源：

TOXICOLOGY | 2005年 / 208卷 / 03期

关键词：

DNA fragmentation; free radicals; intracellular calcium; hepatotoxicity; diethldithiocarbamate; diclofenac; ketoconazol;

D O I：

10.1016/j.tox.2004.11.039

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Sodium diethyldithiocarbamate, diclofenac and ketoconazol are three important chemotherapeutic agents that are commonly associated with hepatotoxicity. This study was undertaken to provide a better understanding of the mechanism through which these drugs induce hepatotoxicity. Some of the possible mechanisms underlying such modulation were investigated. The hepatotoxic activity of sodium diethyldithiocarbamate (800 mg kg(-1)); diclofenac (200 mg kg(-1) 1) and ketoconazol (100 mg kg-1) were investigated in vivo through the assessment of liver functions, lipid peroxidation and histopathological examination. It was found that all drugs have induced severe hepatic damage as evidenced by the elevation serum aminotransferase activities and confirmed by histological changes of liver. In addition, the drug-induced hepatotoxicity was also associated with massive liver DNA fragmentation and an increase in lipid peroxidation. These results strongly suggest a positive correlation between hepatotoxicity and DNA fragmentation. Moreover, this study also implicates calcium as a potential mediator of the drug-induced oxidative stress associated with hepatotoxicity. (C) 2004 Elsevier Ireland Ltd. All rights reserved.

引用

页码：367 / 375

页数：9

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