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二硫苏糖醇对四氯化碳促进的肝微粒体悬浮液中NADPH依赖性脂质过氧化的抑制作用。

Dithiothreitol inhibitory effects on carbon tetrachloride-promoted NADPH-dependent lipid peroxidation in liver microsomal suspensions.

作者信息

de Mecca M M, Castro G D, Díaz Gómez M I, Castro J A

机构信息

Centro de Investigaciones Toxicológicas (CEITOX) CITEFA/CONICET, Pcia. de Buenos Aires, Argentina.

出版信息

Res Commun Mol Pathol Pharmacol. 1995 May;88(2):205-13.

PMID:7670852
Abstract

In previous studies from our laboratory evidence was provided that generation in vivo of dithiothreitol (DTT) from DTT tetraacetate (DTTAC) was accompanied with preventive effects against CCl4-induced necrogenic effects on the liver. In that study, we reported the ability of treatment to decrease the intensity of covalent binding (CB) of the CCl4 reactive metabolites to cellular components but no evidence of preventive effects on CCl4-induced lipid peroxidation (LP) was obtained by the diene hyperconjugation technique. Now, we report that DTT at concentrations 1 or 3 mM inhibit at steps of the process after diene conjugation and prior to malondialdehyde formation. One of those steps might involve peroxides since we observed that DTT is able to significantly react with benzoyl peroxide in a model system. Others might also involve free radicals for in the present study we observed the reaction of DTT with trichloromethyl or trichloromethylperoxy free radicals generated from CBrCl3 in a model system. Reactions of DTT with free radicals and peroxides resulting in inhibition of CB and LP might be critical components in the preventive effects of DTTAC against CCl4-induced liver damage.

摘要

在我们实验室之前的研究中,有证据表明二硫苏糖醇四乙酸酯(DTTAC)在体内生成二硫苏糖醇(DTT)时,伴随着对四氯化碳(CCl4)诱导的肝脏坏死效应的预防作用。在该研究中,我们报告了治疗能够降低CCl4反应性代谢产物与细胞成分的共价结合(CB)强度,但通过二烯超共轭技术未获得对CCl4诱导的脂质过氧化(LP)的预防作用的证据。现在,我们报告1或3 mM浓度的DTT在二烯共轭后和丙二醛形成之前的过程步骤中具有抑制作用。其中一个步骤可能涉及过氧化物,因为我们观察到在模型系统中DTT能够与过氧化苯甲酰发生显著反应。其他步骤也可能涉及自由基,因为在本研究中我们观察到在模型系统中DTT与由三溴氯甲烷产生的三氯甲基或三氯甲基过氧自由基发生反应。DTT与自由基和过氧化物的反应导致CB和LP的抑制,这可能是DTTAC对CCl4诱导的肝损伤预防作用的关键组成部分。

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