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在水相和脂相引发的脂质体过氧化过程中,谷胱甘肽与一种脂溶性抗氧化剂和一种水溶性抗氧化剂的协同抗氧化作用。

The cooperative antioxidant role of glutathione with a lipid-soluble and a water-soluble antioxidant during peroxidation of liposomes initiated in the aqueous phase and in the lipid phase.

作者信息

Barclay L R

机构信息

Department of Chemistry, Mount Allison University, Sackville, New Brunswick, Canada.

出版信息

J Biol Chem. 1988 Nov 5;263(31):16138-42.

PMID:3182788
Abstract

A study is made of the effect of GSH as a co-antioxidant with vitamin E during free radical chain autoxidation inhibition studies of dilinoleoylphosphatidylcholine (DLPC) liposomes. Oxidations are initiated in the aqueous phase with azobis(2-amidinopropane hydrochloride) and in the bilayer phase of DLPC with azobis(2,4-dimethylvaleronitrile) under known conditions of the rate of free radical chain initiation (Ri). In reactions initiated in the aqueous phase, GSH is not an efficient antioxidant when acting alone; however, in cooperation with vitamin E in the bilayers, it does effect significant extensions of the efficient induction period of vitamin E. Quantitative studies show that GSH "spares" 0.4 molecules of vitamin E in the bilayer/molecule of GSH and therefore terminates approximately 0.8 peroxyl radical chains as a co-antioxidant with vitamin E. In contrast, GSH is not an effective co-antioxidant with an efficient water-soluble antioxidant, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylate (Trolox). GSH spares only 0.08 molecules of Trolox/molecule of GSH during autoxidation initiated in the aqueous phase with azobis(2-amidinopropane hydrochloride). The inhibition rate constant for GSH in trapping aqueous phase peroxyls is at least an order of magnitude less than that of Trolox. When peroxidation is initiated in the bilayer phase of DLPC with azobis(2,4-dimethylvaleronitrile), GSH is not an effective co-antioxidant with either vitamin E in the bilayer or Trolox in the water. Comparatively higher ratios of GSH to E (GSH/E = 50) or Trolox (GSH/Trolox = 30) are required to give significant extensions of the E or Trolox induction periods. GSH is estimated to preserve only approximately one vitamin E or Trolox molecule for a hundred GSH for peroxidations initiated in the DLPC bilayers. From the kinetic studies and GSH decay studies during inhibition periods, it is concluded that GSH does not act synergistically by regenerating ArOH from the phenoxyl, ArO, radical of vitamin E or Trolox. The mode of antioxidant action of GSH is concluded to be that of trapping peroxyl radicals in the aqueous phase and thereby indirectly sparing vitamin E in the bilayer.

摘要

在二亚油酰磷脂酰胆碱(DLPC)脂质体的自由基链自氧化抑制研究中,对谷胱甘肽(GSH)作为维生素E的协同抗氧化剂的作用进行了研究。在已知自由基链引发速率(Ri)的条件下,用偶氮二(2-脒基丙烷盐酸盐)在水相中引发氧化反应,用偶氮二(2,4-二甲基戊腈)在DLPC的双分子层相中引发氧化反应。在水相中引发的反应中,单独作用时GSH不是一种有效的抗氧化剂;然而,在双分子层中与维生素E协同作用时,它确实能显著延长维生素E的有效诱导期。定量研究表明,在双分子层中,每分子GSH“节省”0.4分子维生素E,因此作为与维生素E的协同抗氧化剂,它能终止约0.8个过氧自由基链。相比之下,GSH与一种有效的水溶性抗氧化剂6-羟基-2,5,7,8-四甲基苯并二氢吡喃-2-羧酸酯(Trolox)不是有效的协同抗氧化剂。在用偶氮二(2-脒基丙烷盐酸盐)在水相中引发自氧化反应时,每分子GSH仅能节省0.08分子Trolox。GSH捕获水相过氧自由基的抑制速率常数至少比Trolox低一个数量级。当用偶氮二(2,4-二甲基戊腈)在DLPC的双分子层相中引发过氧化反应时,GSH与双分子层中的维生素E或水中的Trolox都不是有效的协同抗氧化剂。需要相对较高的GSH与E的比例(GSH/E = 50)或GSH与Trolox的比例(GSH/Trolox = 30)才能显著延长E或Trolox的诱导期。据估计,对于在DLPC双分子层中引发的过氧化反应,每一百个GSH分子只能保护大约一个维生素E分子或Trolox分子。从抑制期的动力学研究和GSH衰减研究得出结论,GSH不是通过从维生素E或Trolox的苯氧基自由基ArO再生ArOH来发挥协同作用。GSH的抗氧化作用模式被认为是在水相中捕获过氧自由基,从而间接节省双分子层中的维生素E。

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