The effects of resveratrol on cyclooxygenase-1 and cyclooxygenase-2 mRNA and protein levels in diabetic rat kidneys

被引:0
作者
Atiye Seda Yar
Sevda Menevse
Ebru Alp
Fatma Helvacioglu
Gulnur Take
机构
[1] Gazi University,Department of Medical Biology and Genetics, Faculty of Medicine
[2] Gazi University,Department of Histology and Embriology, Faculty of Medicine
来源
Molecular Biology Reports | 2010年 / 37卷
关键词
COX-1; COX-2; Diabetes mellitus; Streptozotocin; Resveratrol;
D O I
暂无
中图分类号
学科分类号
摘要
Cyclooxygenase (COX), which have the isoforms of COX-1 and COX-2, is the key enzyme of prostaglandins biosynthesis. Especially, COX-2 is induced in inflammatory disease such as Diabetes Mellitus (DM). Resveratrol (RSV), a natural antioxidant, has a beneficial role in prevention of inflammatory disease. We investigated the changes of COX-1 and COX-2 mRNA expression and protein level in diabetic rat kidney after RSV treatment. Three months-old, 44 Wistar albino male rats, which were divided into six groups such as control group, sodium citrate buffer (sham control) group, diabetic group (DM), Dimethyl Sulfoxide induced control group, RSV treated sham control group (RSV) and RSV treated diabetic group (DM + RSV) were used for the study. Experimental diabetes was induced by intraperitoneal injection of 55 mg/kg Streptozotocin. After the induction of chronic diabetes 10 mg/kg per day RSV was administered intraperitoneally for 4 weeks. In this study. RSV has no significant effect on COX-1 mRNA expression in diabetic rat kidney (P > 0.05). Immunohistochemical study showed that COX-1 expression was slightly inhibited in RSV group and was not significantly supressed in DM + RSV group. When comparing control and treated groups, there were no significant differences in COX-2 mRNA or protein levels (P > 0.05). In conclusion, our results indicate that resveratrol do not significantly affect COX gene and protein expression. Therefore, different therapy strategies such as combination with other antidiabetic drugs may tried in STZ induced animal model for reducing diabetic symptoms and altering COX-1 and COX-2 mRNA or protein levels.
引用
收藏
页码:2323 / 2331
页数:8
相关论文
共 110 条
[1]  
Vane JR(1998)Cyclooxygenase 1 and 2 Annu Rev Pharmacol Toxicol 38 97-120
[2]  
Bakhle YS(2000)Cyclooxygenases: structural, cellular and molecular biology Annu Rev Biochem 69 145-182
[3]  
Botting RM(1996)Prostaglandin endoperoxide H synthases (cyclooxygenases)-1 and -2 J Biol Chem 271 33157-33160
[4]  
Smith WL(1998)Cyclooxygenase in biology and disease FASEB J 12 1063-1073
[5]  
DeWitt DL(2004)Report of the expert committe on the diagnosis and classification of DM Diabetes Care 27 5-10
[6]  
Garavito RM(1994)The pathogenesis of insulin-dependent diabetes mellitus N Engl J Med 331 1428-1436
[7]  
Smith WL(2006)Diabetes, glucose toxicity, and oxidative stress: a case of double jeopardy for the pancreatic islet beta cell Free Radic Biol Med 41 177-184
[8]  
Garavito RM(2000)Effect of resveratrol, a natural polyphenolic compound, on reactive oxygen species and prostaglandin production Biochem Pharmacol 59 865-870
[9]  
DeWitt DL(2004)Resveratrol is a peroxidase-mediated inactivator of COX-1 but not COX-2 J Biol Chem 279 22727-22737
[10]  
Dubois RN(2000)Biological effects of resveratrol Life Sci 66 663-673