Nordihydroguairetic acid, a lignin, prevents oxidative stress and the development of diabetic nephropathy in rats

被引:44
作者
Anjaneyulu, M [1 ]
Chopra, K [1 ]
机构
[1] Panjab Univ, Univ Inst Pharmaceut Sci, Div Pharmacol, Chandigarh 160014, India
关键词
diabetic nephropathy; oxidative stress; nordihydroguairetic acid; lipid peroxidation; streptozotocin;
D O I
10.1159/000078631
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recent evidences indicate a pivotal role of reactive oxygen species in etiology of diabetic nephropathy, an important microvascular complication of diabetes mellitus. Moreover, oxidative stress leads to an increased production of lipoxygenase derivatives which also play a role in diabetic nephropathy. The present study was thus designed to examine the effect of an antioxidant and a lipoxygenase inhibitor, nordihydroguairetic acid ( NDGA), on renal function and oxidative stress in streptozotocin (STZ)-induced diabetic rats. Diabetes was induced by a single intraperitoneal injection of streptozotocin (65 mg/kg) in rats. After the 4th week of STZ injection, NDGA (5 and 10 mg/kg) was given subcutaneously (s.c.) for another 4 weeks to both control and diabetic rats. At the end of the 8th week, diabetic rats exhibited renal dysfunction as evidenced by reduced creatinine and urea clearance along with enhanced albumin excretion rate as compared with control rats. Biochemical analysis of kidneys revealed a marked increase in oxidative stress demonstrated by increased lipid peroxidation and decreased activities of key antioxidant enzymes, glutathione (GSH), superoxide dismutase ( SOD) and catalase in diabetic rats. Chronic treatment with NDGA in diabetic rats significantly prevented both renal dysfunction and oxidative stress as compared with vehicle-treated diabetic rats. The kidneys of diabetic rats showed morphological changes such as hyaline casts, glomerular thickening and moderate interstitial fibrosis and arteriolopathy, whereas NDGA administration in diabetic rats markedly prevented renal morphological alterations. These results emphasize the role of oxidative stress in the pathophysiology of diabetic nephropathy and point towards the potential of NDGA as a complementary therapy for the prevention/treatment of diabetic nephropathy. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:42 / 50
页数:9
相关论文
共 44 条
[1]   Association of systolic blood pressure with macrovascular and microvascular complications of type 2 diabetes (UKPDS 36): prospective observational study [J].
Adler, AI ;
Stratton, IM ;
Neil, HAW ;
Yudkin, JS ;
Matthews, DR ;
Cull, CA ;
Wright, AD ;
Turner, RC ;
Holman, RR .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7258) :412-419
[2]   Studies on gastrointestinal tract functional changes in diabetic animals [J].
Anjaneyulu, M ;
Ramarao, P .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2002, 24 (02) :71-75
[3]   Nordihydroguairetic acid is a potent inhibitor of ferric-nitrilotriacetate-mediated hepatic and renal toxicity, and renal tumour promotion, in mice [J].
Ansar, S ;
Iqbal, M ;
Athar, M .
CARCINOGENESIS, 1999, 20 (04) :599-606
[4]   Dehydroepiandrosterone protects tissues of streptozotocin-treated rats against oxidative stress [J].
Aragno, M ;
Tamagno, E ;
Gatto, V ;
Brignardello, E ;
Parola, S ;
Danni, O ;
Boccuzzi, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (11-12) :1467-1474
[5]   INCREASE IN THE GLUCOSYLATED FORM OF ERYTHROCYTE CU-ZN-SUPEROXIDE DISMUTASE IN DIABETES AND CLOSE ASSOCIATION OF THE NONENZYMATIC GLUCOSYLATION WITH THE ENZYME-ACTIVITY [J].
ARAI, K ;
IIZUKA, S ;
TADA, Y ;
OIKAWA, K ;
TANIGUCHI, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 924 (02) :292-296
[6]   INHIBITION OF BENZOYL PEROXIDE-MEDIATED TUMOR PROMOTION IN 7,12-DIMETHYLBENZ(A)ANTHRACENE-INITIATED SKIN OF SENCAR MICE BY ANTIOXIDANTS NORDIHYDROGUAIARETIC ACID AND DIALLYL SULFIDE [J].
ATHAR, M ;
RAZA, H ;
BICKERS, DR ;
MUKHTAR, H .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 94 (02) :162-165
[7]   ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[8]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[9]   Interaction of metabolic and haemodynamic factors in mediating experimental diabetic nephropathy [J].
Cooper, ME .
DIABETOLOGIA, 2001, 44 (11) :1957-1972
[10]   THROMBOXANE IN THE PATHOGENESIS OF GLOMERULAR INJURY IN DIABETES [J].
CRAVEN, PA ;
MELHEM, MF ;
DERUBERTIS, FR .
KIDNEY INTERNATIONAL, 1992, 42 (04) :937-946