Modification of cardiac oxidative stress in alloxan-induced diabetic rabbits with repaglinide treatment

被引:12
作者
Gumieniczek, A [1 ]
机构
[1] Med Univ Lublin, Dept Med Chem, PL-20090 Lublin, Poland
关键词
alloxan-induced diabetes; repaglinide; heart; antioxidative system;
D O I
10.1016/j.lfs.2005.04.074
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The aim of this study was to analyze the antioxidative effect of repaglinide in the heart of alloxan-induced diabetic rabbits. The activities of superoxide dismutase (Cu,Zn-SOD), catalase (CAT), glutathione peroxidase (GSH-Px), glutathione reductase (GSSG-R), glutathione (GSH), ascorbic acid (AA), products of lipid peroxidation (LPO) and protein carbonyl groups (PCG) were estimated after 4 and 8 weeks of repaglinide treatment (1 mg daily). At significance level p < 0.05, in diabetic heart the activities of Cu,Zn-SOD and CAT were elevated as compared to control values (by 60.7% and 55.3% for Cu,Zn-SOD, and by 89.7% and 77.4% for CAT after 4 and 8 weeks, respectively). The level of AA was diminished by 52.5% and 41.5% while GSH-Px and GSSG-R activities were decreased after 4 weeks of experiment (by 11.5% and 14.4%, respectively). GSH level was diminished by 33.2% after 8 weeks. Simultaneously, in diabetic heart the levels of LPO and PCG were elevated as compared to control values (by 51.6% and 111.3% for LPO, and by 72.0% and 132.9% for PCG after 4 and 8 weeks, respectively). In diabetic animals, repaglinide normalized GSH-Px activity and GSH level. It modified the activities of Cu,Zn-SOD, CAT and AA as compared to diabetic non-treated animals. In diabetic-treated rabbits the level of LPO was diminished as compared to diabetic non-treated animals, while the level of PCG was not affected. In the present study, repaglinide did not affect blood glucose and plasma insulin concentrations in diabetic rabbits. Nevertheless, the drug showed some beneficial antioxidative properties in the heart tissue. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:259 / 263
页数:5
相关论文
共 22 条
  • [1] AEBI H, 1984, METHOD ENZYMOL, V105, P121
  • [2] Leukocyte lipid peroxidation, superoxide dismutase, glutathione peroxidase and serum and leukocyte vitamin C levels of patients with type II diabetes mellitus
    Akkus, I
    Kalak, S
    Vural, H
    Caglayan, O
    Menekse, E
    Can, G
    Durmus, B
    [J]. CLINICA CHIMICA ACTA, 1996, 244 (02) : 221 - 227
  • [3] Diabetic cardiomyopathy: A metabolic perspective
    Avogaro, A
    de Kreutzenberg, SV
    Negut, C
    Tiengo, A
    Scognamiglio, R
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (8A) : 13A - 16A
  • [4] Oxidative damage and altered antioxidant enzyme activities in the small intestine of streptozotocin-induced diabetic rats
    Bhor, VM
    Raghuram, N
    Sivakami, S
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (01) : 89 - 97
  • [5] Lipid peroxidation and antioxidant status in experimental diabetes
    Feillet-Coudray, C
    Rock, E
    Coudray, C
    Grzelkowska, K
    Azais-Braesco, V
    Dardevet, D
    Mazur, A
    [J]. CLINICA CHIMICA ACTA, 1999, 284 (01) : 31 - 43
  • [6] Effects of repaglinide on oxidative stress in tissues of diabetic rabbits
    Gumieniczek, A
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 2005, 68 (02) : 89 - 95
  • [7] Gumieniczek A, 2002, ACTA BIOCHIM POL, V49, P529
  • [8] HYDROXYL RADICAL SCAVENGING AND ANTIPSORIATIC ACTIVITY OF BENZOIC-ACID DERIVATIVES
    HASELOFF, RF
    BLASIG, IE
    MEFFERT, H
    EBERT, B
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (02) : 111 - 115
  • [9] Free radical scavenging activity of sulfonylureas: A clinical assessment of the effect of gliclazide
    Jennings, PE
    Belch, JJF
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2000, 49 (02): : 23 - 26
  • [10] SIMPLE COLORIMETRIC METHOD FOR ASCORBIC-ACID DETERMINATION IN BLOOD-PLASMA
    KYAW, A
    [J]. CLINICA CHIMICA ACTA, 1978, 86 (02) : 153 - 157