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抗氧化剂及结构相关化合物与线粒体氧化磷酸化的相互作用

The interaction of antioxidants and structurally related compounds with mitochondrial oxidative phosphorylation.

作者信息

Fusi F, Valoti M, Sgaragli G, Murphy M P

机构信息

Department of Biochemistry, Trinity College, Dublin, Ireland.

出版信息

Methods Find Exp Clin Pharmacol. 1991 Nov;13(9):599-603.

PMID:1787767
Abstract

The antioxidants, butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT), interact with mitochondrial oxidative phosphorylation in two ways. They uncouple phosphorylation from oxidation by making the mitochondrial inner membrane more permeable to protons. They also inhibit respiration by a direct interaction with the electron transport chain. Here we separated out these two properties of BHA and BHT by determining their effects on respiration in coupled and uncoupled mitochondria. Similar experiments were carried out with compounds structurally related to BHA and BHT. Most of these compounds had uncoupling and inhibitory properties essentially similar to BHA and BHT. In contrast, the dimer of BHA had no inhibitory effects on uncoupled respiration and little uncoupling activity. The implications of these results for the interactions of BHA and BHT with mitochondrial oxidative phosphorylation and the design of antioxidants are discussed.

摘要

抗氧化剂丁基羟基茴香醚(BHA)和丁基化羟基甲苯(BHT)通过两种方式与线粒体氧化磷酸化相互作用。它们通过使线粒体内膜对质子更具渗透性,使磷酸化与氧化解偶联。它们还通过与电子传递链直接相互作用来抑制呼吸作用。在这里,我们通过测定BHA和BHT对偶联和解偶联线粒体呼吸的影响,分离出了它们的这两种特性。对与BHA和BHT结构相关的化合物进行了类似的实验。这些化合物大多具有与BHA和BHT基本相似的解偶联和抑制特性。相比之下,BHA的二聚体对解偶联呼吸没有抑制作用,且解偶联活性很小。讨论了这些结果对BHA和BHT与线粒体氧化磷酸化相互作用以及抗氧化剂设计的意义。

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