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R-硫辛酸对丁硫氨酸亚砜亚胺诱导的新生大鼠白内障形成的立体特异性作用。

Stereospecific effects of R-lipoic acid on buthionine sulfoximine-induced cataract formation in newborn rats.

作者信息

Maitra I, Serbinova E, Tritschler H J, Packer L

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley, 94720-3200, USA.

出版信息

Biochem Biophys Res Commun. 1996 Apr 16;221(2):422-9. doi: 10.1006/bbrc.1996.0611.

Abstract

This study revealed a marked stereospecificity in the prevention of buthionine sulfoximine-induced cataract, and in the protection of lens antioxidants, in newborn rats by alpha-lipoate, R- and racemic alpha-lipoate decreased cataract formation from 100% (buthionine sulfoximine only) to 55% (buthionine sulfoximine + R-alpha-lipoic acid) and 40% (buthionine sulfoximine + rac-alpha-lipoic acid) (p<0.05 compared to buthionine sulfoximine only). S-alpha-lipoic acid had no effect on cataract formation induced by buthionine sulfoximine. The lens antioxidants glutathione, ascorbate, and vitamin E were depleted to 45, 62, and 23% of control levels, respectively, by buthionine sulfoximine treatment, but were maintained at 84-97% of control levels when R-alpha-lipoic acid or rac-alpha-lipoic acid were administered with buthionine sulfoximine; S-alpha-lipoic acid administration had no protective effect on lens antioxidants. When enantiomers of alpha-lipoic acid were administered to animals, R-alpha-lipoic acid was taken up by lens and reached concentrations 2- to 7-fold greater than those of S-alpha-lipoic acid, with rac-alpha-lipoic acid reaching levels midway between the R-isomer and racemic form. Reduced lipoic acid, dihydrolipoic acid, reached the highest levels in lens of the rac-alpha-lipoic acid-treated animals and the lowest levels in S-alpha-lipoic acid-treated animals. These results indicate that the protective effects of alpha-lipoic acid against buthionine sulfoximine-induced cataract are probably due to its protective effects on lens antioxidants, and that the stereospecificity exhibited is due to selective uptake and reduction of R-alpha-lipoic acid by lens cells.

摘要

本研究揭示了α-硫辛酸在预防新生大鼠丁硫氨酸亚砜亚胺诱导的白内障以及保护晶状体抗氧化剂方面具有显著的立体特异性。R-α-硫辛酸和消旋α-硫辛酸可使白内障形成率从100%(仅丁硫氨酸亚砜亚胺)分别降至55%(丁硫氨酸亚砜亚胺+R-α-硫辛酸)和40%(丁硫氨酸亚砜亚胺+消旋α-硫辛酸)(与仅用丁硫氨酸亚砜亚胺相比,p<0.05)。S-α-硫辛酸对丁硫氨酸亚砜亚胺诱导的白内障形成没有影响。丁硫氨酸亚砜亚胺处理使晶状体抗氧化剂谷胱甘肽、抗坏血酸和维生素E分别降至对照水平的45%、62%和23%,但当R-α-硫辛酸或消旋α-硫辛酸与丁硫氨酸亚砜亚胺一起给药时,它们维持在对照水平的84 - 97%;给予S-α-硫辛酸对晶状体抗氧化剂没有保护作用。当将α-硫辛酸的对映体给予动物时,R-α-硫辛酸被晶状体摄取,其浓度比S-α-硫辛酸高2至7倍,消旋α-硫辛酸达到的水平介于R-异构体和消旋形式之间。还原型硫辛酸,即二氢硫辛酸,在消旋α-硫辛酸处理的动物晶状体中达到最高水平,在S-α-硫辛酸处理的动物晶状体中达到最低水平。这些结果表明,α-硫辛酸对丁硫氨酸亚砜亚胺诱导的白内障的保护作用可能归因于其对晶状体抗氧化剂的保护作用,并且所表现出的立体特异性是由于晶状体细胞对R-α-硫辛酸的选择性摄取和还原。

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