Diabetes-induced apoptosis in rat kidney

被引:67
作者
Zhang, WP
Khanna, P
Chan, LL
Campbell, G
Ansari, NH
机构
[1] UNIV TEXAS,MED BRANCH,DEPT BIOL CHEM & GENET,GALVESTON,TX 77555
[2] UNIV TEXAS,MED BRANCH,DEPT PATHOL,GALVESTON,TX 77555
关键词
D O I
10.1006/bmme.1997.2592
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
Oxidative stress has been suggested to play a crucial role in the pathogenesis of diabetic complications including nephropathy. However, the exact mechanism of diabetic nephropathy is still not clearly understood, Since oxidative stress is known to be a major component in the induction of apoptosis, we investigated the occurrence of apoptosis in diabetic rat kidney. The status of oxidative stress was determined as thiobarbituric acid reactive substances (TBARS). The TBARS in the control and diabetic rat kidney were 2.00 +/- 0.963 and 3.83 +/- 0.715 mu mol/mg protein, respectively (P < 0.05). Apoptosis was determined by evaluating the DNA fragmentation using an enzyme-linked immunoassay and in situ end labeling. DNA fragmentation increased approximately four-fold in diabetic rat kidney compared to the normal kidney (P < 0.05). Apoptag in situ labeling displayed negligible apoptosis in nondiabetic kidney while significant areas of apoptosis were observed in diabetic kidney. Our results suggest that increased oxidative stress in diabetic kidney could induce apoptosis, which may contribute to the development of diabetic nephropathy. (C) 1997 Academic Press.
引用
收藏
页码:58 / 62
页数:5
相关论文
共 23 条
  • [1] LIPID-PEROXIDATION AND RETINOPATHY IN STREPTOZOTOCIN-INDUCED DIABETES
    ARMSTRONG, D
    ALAWADI, F
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1991, 11 (04) : 433 - 436
  • [2] BAUGARTNERPARZE.SM, 1995, DIABETES, V44, P1323
  • [3] OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS
    BUTTKE, TM
    SANDSTROM, PA
    [J]. IMMUNOLOGY TODAY, 1994, 15 (01): : 7 - 10
  • [4] COHEN JJ, 1992, ANNU REV IMMUNOL, V10, P267, DOI 10.1146/annurev.iy.10.040192.001411
  • [5] Glucose may induce cell death through a free radical-mediated mechanism
    Donnini, D
    Zambito, AM
    Perrella, G
    AmbesiImpiombato, FS
    Curcio, F
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 219 (02) : 412 - 417
  • [6] GIORDANO C, 1995, DIABETOLOGIA, V38, P953, DOI 10.1007/BF00400585
  • [7] JAIN SK, 1984, J BIOL CHEM, V259, P3391
  • [8] JAIN SK, 1989, J BIOL CHEM, V264, P21340
  • [9] EFFECT OF HIGH GLUCOSE ON CELLULAR PROLIFERATION AND LIPID-PEROXIDATION IN CULTURED VERO CELLS
    KANNAN, K
    JAIN, SK
    [J]. HORMONE AND METABOLIC RESEARCH, 1994, 26 (07) : 322 - 325
  • [10] Glycation, oxidative stress, and scavenger activity glucose metabolism and radical scavenger dysfunction in endothelial cells
    Kashiwagi, A
    Asahina, T
    Nishio, Y
    Ikebuchi, M
    Tanaka, Y
    Kikkawa, R
    Shigeta, Y
    [J]. DIABETES, 1996, 45 : S84 - S86