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二氢硫辛酸——一种在膜相和水相中均具有普遍抗氧化作用的物质。可还原过氧自由基、抗坏血酸自由基和色满氧基自由基。

Dihydrolipoic acid--a universal antioxidant both in the membrane and in the aqueous phase. Reduction of peroxyl, ascorbyl and chromanoxyl radicals.

作者信息

Kagan V E, Shvedova A, Serbinova E, Khan S, Swanson C, Powell R, Packer L

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720.

出版信息

Biochem Pharmacol. 1992 Oct 20;44(8):1637-49. doi: 10.1016/0006-2952(92)90482-x.

Abstract

Thioctic (lipoic) acid is used as a therapeutic agent in a variety of diseases in which enhanced free radical peroxidation of membrane phospholipids has been shown to be a characteristic feature. It was suggested that the antioxidant properties of thioctic acid and its reduced form, dihydrolipoic acid, are at least in part responsible for the therapeutic potential. The reported results on the antioxidant efficiency of thioctic and dihydrolipoic acids obtained in oxidation models with complex multicomponent initiation systems are controversial. In the present work we used relatively simple oxidation systems to study the antioxidant effects of dihydrolipoic and thioctic acids based on their interactions with: (1) peroxyl radicals which are essential for the initiation of lipid peroxidation, (2) chromanoxyl radicals of vitamin E, and (3) ascorbyl radicals of vitamin C, the two major lipid- and water-soluble antioxidants, respectively. We demonstrated that: (1) dihydrolipoic acid (but not thioctic acid) was an efficient direct scavenger of peroxyl radicals generated in the aqueous phase by the water-soluble azoinitiator 2,2'-azobis(2-amidinopropane)-dihydrochloride, and in liposomes or in microsomal membranes by the lipid-soluble azoinitiator 2,2'-azobis(2,4-dimethylvaleronitrile); (2) both dihydrolipoic acid and thioctic acid did not interact directly with chromanoxyl radicals of vitamin E (or its synthetic homologues) generated in liposomes or in the membranes by three different ways: UV-irradiation, peroxyl radicals of 2,2'-azobis(2,4-dimethylvaleronitrile), or peroxyl radicals of linolenic acid formed by the lipoxygenase-catalyzed oxidation; and (3) dihydrolipoic acid (but not thioctic acid) reduced ascorbyl radicals (and dehydroascorbate) generated in the course of ascorbate oxidation by chromanoxyl radicals. This interaction resulted in ascorbate-mediated dihydrolipoic acid-dependent reduction of the vitamin E chromanoxyl radicals, i.e. vitamin E recycling. We conclude that dihydrolipoic acid may act as a strong direct chain-breaking antioxidant and may enhance the antioxidant potency of other antioxidants (ascorbate and vitamin E) in both the aqueous and the hydrophobic membraneous phases.

摘要

硫辛酸在多种疾病中用作治疗剂,在这些疾病中,膜磷脂的自由基过氧化增强已被证明是一个特征性特点。有人认为硫辛酸及其还原形式二氢硫辛酸的抗氧化特性至少部分地决定了其治疗潜力。在具有复杂多组分引发体系的氧化模型中获得的关于硫辛酸和二氢硫辛酸抗氧化效率的报道结果存在争议。在本研究中,我们使用相对简单的氧化体系,基于二氢硫辛酸和硫辛酸与以下物质的相互作用来研究它们的抗氧化作用:(1)脂质过氧化引发所必需的过氧自由基;(2)维生素E的色满氧自由基;(3)维生素C的抗坏血酸自由基,它们分别是两种主要的脂溶性和水溶性抗氧化剂。我们证明:(1)二氢硫辛酸(而非硫辛酸)是水溶性偶氮引发剂2,2'-偶氮二(2-脒基丙烷)二盐酸盐在水相中产生的过氧自由基以及脂溶性偶氮引发剂2,2'-偶氮二(2,4-二甲基戊腈)在脂质体或微粒体膜中产生的过氧自由基的有效直接清除剂;(2)二氢硫辛酸和硫辛酸都不与通过三种不同方式在脂质体或膜中产生的维生素E的色满氧自由基(或其合成类似物)直接相互作用:紫外线照射、2,2'-偶氮二(2,4-二甲基戊腈)的过氧自由基或脂氧合酶催化氧化形成的亚麻酸过氧自由基;(3)二氢硫辛酸(而非硫辛酸)还原了色满氧自由基在抗坏血酸氧化过程中产生的抗坏血酸自由基(和脱氢抗坏血酸)。这种相互作用导致抗坏血酸介导的二氢硫辛酸依赖性维生素E色满氧自由基的还原,即维生素E循环。我们得出结论,二氢硫辛酸可能作为一种强大的直接链断裂抗氧化剂,并且可以在水相和疏水膜相中增强其他抗氧化剂(抗坏血酸和维生素E)的抗氧化能力。

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