Dichloromethane potentiation of carbon tetrachloride hepatotoxicity in rats.

Young Chul Kim
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引用次数: 9

Abstract

Concomitant treatment of rats with a nonhepatotoxic dose of dichloromethane (6 mmol/kg, i.p.) significantly potentiated the hepatotoxicity of carbon tetrachloride (2 mmol/kg, i.p.). Toxicity was determined by increases in serum sorbitol dehydrogenase and alanine aminotransferase activities measured 24 hr following the treatments. Dichloromethane did not affect the lipid peroxidation induced by carbon tetrachloride as determined by conjugated diene formation in hepatic microsomal lipids. The covalent binding of [14C]Cl4 metabolites to microsomal lipids was increased significantly by dichloromethane. The results suggest that dichloromethane potentiates carbon tetrachloride hepatotoxicity by increasing covalent binding of its metabolites to hepatic microsomal lipids.
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二氯甲烷对四氯化碳肝毒性的增强作用。
同时给予大鼠无肝毒性剂量的二氯甲烷(6 mmol/kg, i.p)显著增强了四氯化碳(2 mmol/kg, i.p)的肝毒性。毒性通过治疗24小时后测定血清山梨醇脱氢酶和丙氨酸转氨酶活性的增加来确定。二氯甲烷不影响四氯化碳诱导的脂质过氧化,通过肝微粒体脂质中偶联二烯的形成来确定。二氯甲烷显著增加了[14C]Cl4代谢物与微粒体脂质的共价结合。结果表明,二氯甲烷通过增加其代谢物与肝微粒体脂质的共价结合,增强了四氯化碳的肝毒性。
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