Hyperglycemia induced oxidative stress in type-1 and type-2 diabetic patients with and without nephropathy

被引:64
作者
Dave, G. S. [1 ]
Kalia, K. [1 ]
机构
[1] Sardar Patel Univ, Dept Biosci, Vallabh Vidyanagar 388120, Gujarat, India
关键词
type-1 and type-2 diabetes mellitus; nephropathy; oxidative stress;
D O I
10.1170/T820
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
Diabetes mellitus is associated with hyperglycemia, hyperlipoproteinaemia and oxidative stress at cellular level. The aim of the present study was to determine the relationship between anti-oxidative system of cells and hyperglycemia induced reactive oxygen species (ROS) in type-1 and type-2 diabetic patients with and without nephropathy. ROS are anihilated by an intracellular enzymatic system such as glutathione peroxidase (GPx) and catalase and the reduced glutathione (GSH) is the major antioxidant of erythrocytes and plasma. Total of 200 diabetic patients and 50 of normal healthy control individuals were recruited for the present study. Erythrocytes and plasma activities of GPx, catalase and GSH were measured as a part of anti-oxidative system and TBARS for the marker of oxidative stress in type-1 diabetes mellitus (T1DM), type-2 diabetic mellitus (T2DM), type-1 diabetes with nephropathy (T1DN) and type-2 diabetes with nephropathy (T2DN) patients. GPx, catalase and GSH activity was significantly decreased, whereas TBARS level was significantly increased in both type-1 and type-2 diabetic groups with and without nephropathy than the normal healthy individuals. T1DM patients had shown decreased level of GSH and activity of anti-oxidative enzymes than T2 DM patients, whereas TBARS level was higher in T1DM than T2DM patients, suggesting that T1DM patients are more prone to secondary complications such as nephropathy than T2DM patients. Obtained results have shown positive correlation of GSH with GPx and catalase activity in erythrocytes and plasma, whereas, negative correlation was observed between TBARS and catalase in erythrocytes and plasma indicative of the relationship of various anti-oxidative enzymes and key antioxidant such as GSH in erythrocytes and plasma responsible for increased oxidative stress.
引用
收藏
页码:68 / 78
页数:11
相关论文
共 48 条
[1]  
ANDERSEN AR, 1983, DIABETOLOGIA, V25, P496
[2]   How hyperglycemia promotes atherosclerosis: molecular mechanisms [J].
Aronson, Doron ;
Rayfield, Elliot J. .
CARDIOVASCULAR DIABETOLOGY, 2002, 1 (1)
[3]  
Atalay Mustafa, 2002, J Sports Sci Med, V1, P1
[4]   HUMAN KIDNEY PROXIMAL TUBULES ARE THE MAIN SOURCE OF PLASMA GLUTATHIONE-PEROXIDASE [J].
AVISSAR, N ;
ORNT, DB ;
YAGIL, Y ;
HOROWITZ, S ;
WATKINS, RH ;
KERL, EA ;
TAKAHASHI, K ;
PALMER, IS ;
COHEN, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02) :C367-C375
[5]   Antioxidant status, lipid peroxidation and nitric oxide end products in patients of type 2 diabetes mellitus with nephropathy [J].
Bhatia, S ;
Shukla, R ;
Madhu, SV ;
Gambhir, JK ;
Prabhu, KM .
CLINICAL BIOCHEMISTRY, 2003, 36 (07) :557-562
[6]   Glucose and reactive oxygen species [J].
Bonnefont-Rousselot, D .
CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE, 2002, 5 (05) :561-568
[7]   Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[8]  
Buege J A, 1978, Methods Enzymol, V52, P302
[9]   Activities of antioxidant scavenger enzymes (Superoxide dismutase and glutathione peroxidase) in erythrocytes in adult women with and without type II diabetes [J].
Carmeli, E ;
Coleman, R ;
Berner, YN .
EXPERIMENTAL DIABESITY RESEARCH, 2004, 5 (02) :171-175
[10]   Defective intracellular antioxidant enzyme production in type 1 diabetic patients with nephropathy [J].
Ceriello, A ;
Morocutti, A ;
Mercuri, F ;
Quagliaro, L ;
Moro, M ;
Damante, G ;
Viberti, GC .
DIABETES, 2000, 49 (12) :2170-2177