Effect of α-lipoic acid on lipid peroxidation and anti-oxidant enzyme activities in diabetic rats

被引:55
作者
Dinçer, Y
Telci, A
Kayali, R
Yilmaz, IA
Çakatay, U
Akçay, T
机构
[1] Istanbul Univ, Istanbul Fac Med, Cent Lab Clin Biochem, Istanbul, Turkey
[2] Istanbul Univ, Cerrahpasa Med Fac, Dept Biochem, Istanbul, Turkey
来源
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY | 2002年 / 29卷 / 04期
关键词
diabetic rats; glutathione peroxidase; glutathione reductase; glutathione; alpha-lipoic acid; superoxide dismutase;
D O I
10.1046/j.1440-1681.2002.03642.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Oxidative damage has been suggested to be a contributory factor in the development and complications of diabetes. Recently, alpha-lipoic acid (ALA) has gained considerable interest as an anti-oxidant. Various studies have indicated the anti- oxidant effects of ALA and its reduced form dihydrolipoic acid. Therefore, it appears that these compounds have important therapeutic potential in conditions where oxidative stress is involved. The aim of the present study was to investigate the effect of ALA supplementation on lipid peroxidation and anti-oxidant enzyme activities in various tissues in diabetic rats. 2. Male Wistar rats were divided into three groups. Diabetes was induced by streptozotocin (STZ) injection in the two groups of rats to be supplemented and not to be supplemented with ALA. Another group of rats, which received saline injection, formed the control group. After 5 weeks of diabetes, rats were killed. In order to assess the redox status of various organs in the diabetic and control rats, thiobarbituric acid-reactive substances (TBARS) and glutathione (GSH) levels, as well as superoxide dismutase (SOD), glutathione peroxidase (G-Px) and glutathione reductase (G-Red) activities were determined in the liver, pancreas and kidney. 3. In both diabetic groups, TBARS levels and SOD activity were increased in the liver and pancreas, G-Px and G-Red activities were increased in the kidney and GSH levels were decreased in all organs compared with controls. In the ALA- supplemented group, TBARS levels were decreased, GSH levels were increased in the liver and pancreas, SOD activity was decreased in the liver, G-Px activity remained unchanged in all tissues and G-Red activity was increased in the pancreas compared with the diabetic group that did not receive ALA supplementation. 4. In conclusion, ALA supplementation has disparate effects on the redox status of different organs. These data are not sufficient for confirmation the beneficial effects of ALA supplementation on the redox status of various organs in diabetic rats.
引用
收藏
页码:281 / 284
页数:4
相关论文
共 25 条
  • [1] Androne L, 2000, IN VIVO, V14, P327
  • [2] PEROXISOMAL OXIDASES IN VARIOUS TISSUES OF DIABETIC RATS
    ASAYAMA, K
    YOKOTA, S
    KATO, K
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 1991, 11 (02) : 89 - 94
  • [3] Bastar I, 1998, RES COMMUN MOL PATH, V102, P265
  • [4] ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES
    BAYNES, JW
    [J]. DIABETES, 1991, 40 (04) : 405 - 412
  • [5] BUSSE E, 1992, ARZNEIMITTELFORSCH, V42-1, P829
  • [6] α-lipoic acid in liver metabolism and disease
    Bustamante, J
    Lodge, JK
    Marcocci, L
    Tritschler, HJ
    Packer, L
    Rihn, BH
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1998, 24 (06) : 1023 - 1039
  • [7] Oxidative protein damage in type I diabetic patients with and without complications
    Çakatay, U
    Telci, A
    Salman, S
    Satman, L
    Sivas, A
    [J]. ENDOCRINE RESEARCH, 2000, 26 (03) : 365 - 379
  • [8] Effect of α-lipoic acid supplementation on oxidative protein damage in the streptozotocin-diabetic rat
    Çakatay, U
    Telci, A
    Kayali, R
    Sivas, A
    Akçay, T
    [J]. RESEARCH IN EXPERIMENTAL MEDICINE, 2000, 199 (04) : 243 - 251
  • [9] TISSUE SULFHYDRYL GROUPS
    ELLMAN, GL
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1959, 82 (01) : 70 - 77
  • [10] Antioxidant role of α-lipoic acid in lead toxicity
    Gurer, H
    Ozgunes, H
    Oztezcan, S
    Ercal, N
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (1-2) : 75 - 81