Antioxidant status, lipid peroxidation and nitric oxide end products in patients of type 2 diabetes mellitus with nephropathy

被引:158
作者
Bhatia, S
Shukla, R [1 ]
Madhu, SV
Gambhir, JK
Prabhu, KM
机构
[1] Univ Coll Med Sci, Dept Biochem, Delhi 110095, India
[2] Guru Teg Bahadur Hosp, Delhi 110095, India
[3] Univ Coll Med Sci, Dept Med, Delhi 110095, India
关键词
oxidative stress; diabetic nephropathy; malondialdehyde; superoxide dismutase; catalase; reduced glutathione; nitric oxide;
D O I
10.1016/S0009-9120(03)00094-8
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Oxidative stress is considered to be a unifying link between diabetes mellitus (DM) and its complications including nephropathy. The aim of the present study was to evaluate oxidative stress status in Asian Indian patients of type 2 DM with nephropathy. Design and Methods: Serum levels of malondialdehyde (MDA) and nitric oxide end products (nitrite and nitrate), activities of erythrocyte superoxide dismutase (SOD), catalase (CAT) and reduced glutathione (GSH) content were estimated in controls, patients of type 2 DM without nephropathy (group 1) and with nephropathy (group 2). Results: Serum MDA concentration was significantly high in both the groups of diabetic patients as compared to controls, (P < 0.05), with group 2 having a significantly higher value than group 1 (p < 0.05). Significantly elevated serum nitrite levels were found in diabetic patients as compared to controls (p < 0.001), however, no significant difference was found between group 1 and group 2. Moreover, serum nitrate as well as nitrite + nitrate levels were significantly higher in group 2 as compared to controls (p < 0.05). Activity of erythrocyte SOD and CAT was significantly reduced in both groups as compared to controls (p < 0.001) with catalase activity in group 2 being significantly lower than group 1 (p < 0.05). Erythrocyte GSH content was significantly lower in group 2 as compared to controls (p < 0.05) and group 1 (p < 0.05). Conclusions: Results of the present study indicate that oxidative stress is increased and antioxidant defenses are compromised in type 2 DM. These derangements are of a higher magnitude in patients of type 2 DM with nephropathy. (C) 2003 The Canadian Society of Clinical Chemists. All rights reserved.
引用
收藏
页码:557 / 562
页数:6
相关论文
共 38 条
[1]   Microalbuminuria in patients with NIDDM: An overview [J].
Alzaid, AA .
DIABETES CARE, 1996, 19 (01) :79-89
[2]  
Arali K, 1987, BIOCHIM BIOPHYS ACTA, V924, P292
[3]   Oxidative stress and nitric oxide related parameters in type II diabetes mellitus:: effects of glycemic control [J].
Aydin, A ;
Orhan, H ;
Sayal, A ;
Özata, M ;
Sahin, G ;
Isimer, A .
CLINICAL BIOCHEMISTRY, 2001, 34 (01) :65-70
[4]   Role of oxidative stress in diabetic complications - A new perspective on an old paradigm [J].
Baynes, JW ;
Thorpe, SR .
DIABETES, 1999, 48 (01) :1-9
[5]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[6]   Total radical-trapping antioxidant parameter in NIDDM patients [J].
Ceriello, A ;
Bortolotti, N ;
Falleti, E ;
Taboga, C ;
Tonutti, L ;
Crescentini, A ;
Motz, E ;
Lizzio, S ;
Russo, A ;
Bartoli, E .
DIABETES CARE, 1997, 20 (02) :194-197
[7]   AN INTRODUCTION TO FREE-RADICAL BIOCHEMISTRY [J].
CHEESEMAN, KH ;
SLATER, TF .
BRITISH MEDICAL BULLETIN, 1993, 49 (03) :481-493
[8]   Increased circulating nitric oxide in young patients with type 1 diabetes and persistent microalbuminuria - Relation to glomerular hyperfiltration [J].
Chiarelli, F ;
Cipollone, F ;
Romano, F ;
Tumini, S ;
Costantini, F ;
di Ricco, L ;
Pomilio, M ;
Pierdomenico, SD ;
Marini, M ;
Cuccurullo, F ;
Mezzetti, A .
DIABETES, 2000, 49 (07) :1258-1263
[9]   FREE-RADICAL ACTIVITY AND HEMOSTATIC FACTORS IN NIDDM PATIENTS WITH AND WITHOUT MICROALBUMINURIA [J].
COLLIER, A ;
RUMLEY, A ;
RUMLEY, AG ;
PATERSON, JR ;
LEACH, JP ;
LOWE, GDO ;
SMALL, M .
DIABETES, 1992, 41 (08) :909-913
[10]   Susceptibility of glutatione and glutathione-related antioxidant activity to hydrogen peroxide in patients with type 2 diabetes:: effect of glycemic control [J].
Dinçer, Y ;
Alademir, Z ;
Ilkova, H ;
Akçay, T .
CLINICAL BIOCHEMISTRY, 2002, 35 (04) :297-301