The effects of resveratrol on cyclooxygenase-1 and-2, nuclear factor kappa beta, matrix metalloproteinase-9, and sirtuin 1 mRNA expression in hearts of streptozotocin-induced diabetic rats

被引:42
作者
Yar, A. S. [1 ]
Menevse, S. [1 ]
Alp, E. [1 ]
机构
[1] Gazi Univ, Fac Med, Dept Med Biol & Genet, Ankara, Turkey
关键词
Diabetes mellitus; COX; NF-kappa B; SIRT1; Resveratrol; MMP-9; SMALL-MOLECULE ACTIVATORS; OXIDATIVE STRESS; TRANS-RESVERATROL; DOWN-REGULATION; SUPPRESSION; COX-2; TRANSCRIPTION; PHYTOALEXIN; INHIBITION; INDUCTION;
D O I
10.4238/2011.November.29.7
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
Resveratrol (RSV) has a beneficial role in the prevention of diabetes and alleviates some diabetic complications, such as cardiomyopathy. We investigated cyclooxygenase-1 (COX-1), COX-2, nuclear factor kappa B (NF-kappa B), matrix metalloproteinase-9 (MMP-9), and sirtuin 1 (SIRT1) mRNA expression levels in heart tissue after RSV treatment in streptozotocin (STZ)-induced diabetic rats. After induction of chronic diabetes with STZ, 10 mg RSV/kg per day was administered to DM and DM+RSV groups for four weeks. At the end of the experiment, all rats were sacrificed and heart tissues were stored at -80 degrees C; mRNA expression levels of COX-1, COX-2, NF-kappa B, MMP-9, and SIRT1 genes were analyzed with quantitative real-time PCR. We did not find any significant effect of RSV on MMP-9, COX-1, COX-2, or NF-kappa B mRNA levels among the groups. However, SIRT1 mRNA levels decreased in the DM group compared to controls and increased in the DM+RSV group when compared to the DM group. SIRT1 is activated by RSV treatment in diabetic heart tissue. Activation of SIRT1 by RSV may lead to a new therapeutic approach for diabetic heart tissue. We conclude that RSV treatment can alleviate heart dysfunction by inhibiton of inflammatory gene expression such as SIRT1.
引用
收藏
页码:2962 / 2975
页数:14
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