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可卡因诱导的肝毒性:脂质过氧化作为一种可能的机制。

Cocaine-induced hepatotoxicity: lipid peroxidation as a possible mechanism.

作者信息

Teaf C M, Freeman R W, Harbison R D

出版信息

Drug Chem Toxicol. 1984;7(4):383-96. doi: 10.3109/01480548408998265.

Abstract

In vitro experiments with hepatic washed microsomal preparations showed that malondialdehyde (MDA) formation was increased in a time- and concentration-dependent manner using COC or NC as the substrate. Though 1 mM COC or NC inhibited MDA formation, significant elevations were observed for 100, 10 or 1 microM concentrations. NC at 10 microM after a 30 minute incubation produced a 34% decrease in hepatic microsomal cytochrome P450 whereas 1 mM NC had no such effect. MDA formation in vivo, measured as total absorbance at 535 nm per gram liver, was found to be maximal 4 hours after 40 mg/kg NC ip. Elevations of serum transaminase (SGPT) however were not found until 6 hours after NC. We conclude from these studies that COC and NC induce lipid peroxidation in the liver of PB-pretreated Swiss-origin mice and that peroxidative attack may be a mechanism for hepatotoxicity of these compounds.

摘要

使用肝洗涤微粒体制剂进行的体外实验表明,以COC或NC作为底物时,丙二醛(MDA)的形成呈时间和浓度依赖性增加。虽然1 mM的COC或NC抑制MDA的形成,但在100、10或1 microM浓度下观察到MDA显著升高。孵育30分钟后,10 microM的NC使肝微粒体细胞色素P450降低了34%,而1 mM的NC则没有这种作用。以每克肝脏在535 nm处的总吸光度来衡量,体内MDA的形成在腹腔注射40 mg/kg NC后4小时达到最大值。然而,直到NC注射6小时后才发现血清转氨酶(SGPT)升高。我们从这些研究中得出结论,COC和NC可诱导经PB预处理的瑞士种小鼠肝脏中的脂质过氧化,且过氧化攻击可能是这些化合物肝毒性的一种机制。

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