Molecular aspects of lipoic acid in the prevention of diabetes complications

被引:570
作者
Packer, L
Kraemer, K
Rimbach, G
机构
[1] Univ So Calif, Sch Pharm, Dept Mol Pharmacol & Toxicol, Los Angeles, CA 90098 USA
[2] BASF AG, D-6700 Ludwigshafen, Germany
[3] Univ Reading, Sch Food Biosci, Hugh Sinclar Human Nutr Unit, Reading, Berks, England
关键词
lipoic acid; diabetes; gene expression; free radicals;
D O I
10.1016/S0899-9007(01)00658-X
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
alpha -Lipoic acid (LA) and its reduced form, dihydrolipoic acid, are powerful antioxidants, LA scavenges hydroxyl radicals, hypochlorous acid, peroxynitrite, and singlet oxygen. Dihydrolipoic acid also scavenges superoxide and peroxyl radicals and can regenerate thioredoxin, vitamin C, and glutathione, which in turn can recycle vitamin E. There are several possible sources of oxidative stress in diabetes including glycation reactions, decompartmentalization of transition metals, and a shift in the reduced-oxygen status of the diabetic cells. Diabetics have increased levels of lipid hydroperoxides, DNA adducts, and protein carbonyls. Available data strongly suggest that LA, because of its antioxidant properties, is particularly suited to the prevention and/or treatment of diabetic complications that arise from an overproduction of reactive oxygen and nitrogen species. In addition to its antioxidant properties, LA increases glucose uptake through recruitment of the glucose transporter-4 to plasma membranes, a mechanism that is shared with insulin-stimulated glucose uptake. Further, recent trials have demonstrated that LA improves glucose disposal in patients with type II diabetes. In experimental and clinical studies, LA markedly reduced the symptoms of diabetic pathologies, including cataract formation, vascular damage, and polyneuropathy. To develop a better understanding of the preventative and therapeutic potentials of LA, much of the current interest is focused on elucidating its molecular mechanisms in redox dependent gene expression. Nutrition 2001;17:888-895. (C) Elsevier Science Inc. 2001.
引用
收藏
页码:888 / 895
页数:8
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