Oxidative damage and altered antioxidant enzyme activities in the small intestine of streptozotocin-induced diabetic rats

被引:161
作者
Bhor, VM [1 ]
Raghuram, N [1 ]
Sivakami, S [1 ]
机构
[1] Univ Bombay, Dept Life Sci, Bombay 400098, Maharashtra, India
关键词
small intestine; diabetes; oxidative stress; antioxidant enzymes; mRNA expression;
D O I
10.1016/S1357-2725(03)00142-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The small intestine exhibits numerous morphological and functional alterations during diabetes. Oxidative stress, a factor implicated in the pathogenesis of diabetic complications may contribute towards some of these alterations. We therefore investigated the occurrence of oxidative stress in the small intestine during diabetes by measuring the extent of oxidative damage as well as the status of the antioxidant defense system. Significant increases in lipid peroxidation (four-fold) as measured by TBARS and protein oxidation (38%) as measured by protein carbonyl content were observed after 6 weeks of diabetes. A distinct elevation in the activities of catalase (123.9%) and superoxide dismutase (71.9%) and a decline in the activity of glutathione peroxidase (67.7%) were also observed. The steady state mRNA levels of these enzymes measured by RT-PCR were, however, unchanged suggesting the absence of transcriptional control. In contrast, no changes in the levels of protein and non-protein thiols as well as the activities of glutathione reductase and glutathione-S-transferase were detected. Interestingly, decreases in the activities of xanthine oxidase (XO; 25.7%) and xanthine dehydrogenase (XDH; 42.6%) indicate that they do not contribute significantly to oxidative damage. The results thus reveal the occurrence of oxidative stress in the small intestine during diabetes and suggest its possible involvement in some of the accompanying functional alterations. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:89 / 97
页数:9
相关论文
共 48 条
  • [1] AEBI HE, 1983, METHOD ENZYMAT AN, V3, P278
  • [2] AWASTHI YC, 1980, BIOCHEM J, V191, P1
  • [3] IDENTIFICATION OF THE SITE OF NONENZYMATIC GLYCATION OF GLUTATHIONE-PEROXIDASE - RATIONALIZATION OF THE GLYCATION-RELATED CATALYTIC ALTERATIONS ON THE BASIS OF 3-DIMENSIONAL PROTEIN-STRUCTURE
    BALDWIN, JS
    LEE, L
    LEUNG, TK
    MURUGANANDAM, A
    MUTUS, B
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 1995, 1247 (01): : 60 - 64
  • [4] Role of oxidative stress in diabetic complications - A new perspective on an old paradigm
    Baynes, JW
    Thorpe, SR
    [J]. DIABETES, 1999, 48 (01) : 1 - 9
  • [5] Baynes JW, 1996, CURR OPIN ENDOCRINOL, V3, P277, DOI DOI 10.1097/00060793-199608000-00001
  • [6] INACTIVATION OF GLUTATHIONE-PEROXIDASE BY SUPEROXIDE RADICAL
    BLUM, J
    FRIDOVICH, I
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 240 (02) : 500 - 508
  • [7] BOUCHIER A, 1993, GASTROENTEROLOGY CLI, V1
  • [8] BRASITUS TA, 1985, J BIOL CHEM, V260, P2405
  • [9] Increased mRNA levels of Mn-SOD and catalase in embryos of diabetic rats from a malformation-resistant strain
    Cederberg, J
    Galli, J
    Luthman, H
    Eriksson, UJ
    [J]. DIABETES, 2000, 49 (01) : 101 - 107
  • [10] The effect of insulin on human small intestinal mucosal protein synthesis
    Charlton, M
    Ahlman, B
    Nair, KS
    [J]. GASTROENTEROLOGY, 2000, 118 (02) : 299 - 306