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丁基羟基茴香醚与线粒体氧化磷酸化的相互作用。

Interaction of butylated hydroxyanisole with mitochondrial oxidative phosphorylation.

作者信息

Fusi F, Sgaragli G, Murphy M P

机构信息

Department of Biochemistry, Trinity College, Dublin, Ireland.

出版信息

Biochem Pharmacol. 1992 Mar 17;43(6):1203-8. doi: 10.1016/0006-2952(92)90493-3.

Abstract

The antioxidant, butylated hydroxyanisole (BHA), has a number of effects on mitochondrial oxidative phosphorylation. In this study we apply the novel approach developed by Brand (Brand MD, Biochim Biophys Acta 1018: 128-133, 1990) to investigate the site of action of BHA on oxidative phosphorylation in rat liver mitochondria. Using this approach we show that BHA increases the proton leak through the mitochondrial inner membrane and that it also inhibits the delta p (proton motive force across the mitochondrial inner membrane) generating system, but has no effect on the phosphorylation system. This demonstrates that compounds having pleiotypic effects on mitochondrial oxidative phosphorylation in vitro can be analysed and their many effects distinguished. This approach is of general use in analysing many other compounds of pharmacological interest which interact with mitochondria. The implications of these results for the mechanism of interaction of BHA with mitochondrial oxidative phosphorylation are discussed.

摘要

抗氧化剂丁基羟基茴香醚(BHA)对线粒体氧化磷酸化有多种作用。在本研究中,我们采用Brand(Brand MD,《生物化学与生物物理学报》1018: 128 - 133,1990)开发的新方法来研究BHA对大鼠肝线粒体氧化磷酸化的作用位点。使用该方法我们发现,BHA增加了质子通过线粒体内膜的泄漏,并且它还抑制了Δp(跨线粒体内膜的质子动力)产生系统,但对磷酸化系统没有影响。这表明,对体外线粒体氧化磷酸化具有多效性作用的化合物可以进行分析,并区分它们的多种作用。这种方法在分析许多其他与线粒体相互作用的具有药理学意义的化合物时具有普遍用途。讨论了这些结果对BHA与线粒体氧化磷酸化相互作用机制的意义。

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