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白藜芦醇对链脲佐菌素诱导的糖尿病大鼠心脏中环氧合酶-1和-2、核因子κB、基质金属蛋白酶-9及沉默信息调节因子1 mRNA表达的影响

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.

作者信息

Yar A S, Menevse S, Alp E

机构信息

Department of Medical Biology and Genetics, Faculty of Medicine, Gazi University, Ankara, Turkey.

出版信息

Genet Mol Res. 2011 Nov 29;10(4):2962-75. doi: 10.4238/2011.November.29.7.

Abstract

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 κB (NF-κB), 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°C; mRNA expression levels of COX-1, COX-2, NF-κB, 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-κB 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.

摘要

白藜芦醇(RSV)在预防糖尿病及缓解某些糖尿病并发症(如心肌病)方面具有有益作用。我们研究了链脲佐菌素(STZ)诱导的糖尿病大鼠经RSV治疗后心脏组织中环氧合酶-1(COX-1)、环氧合酶-2(COX-2)、核因子κB(NF-κB)、基质金属蛋白酶-9(MMP-9)和沉默调节蛋白1(SIRT1)的mRNA表达水平。在用STZ诱导慢性糖尿病后,每天给糖尿病组(DM)和糖尿病+RSV组大鼠按10 mg RSV/kg的剂量给药,持续四周。实验结束时,处死所有大鼠,将心脏组织储存于-80°C;采用定量实时PCR分析COX-1、COX-2、NF-κB、MMP-9和SIRT1基因的mRNA表达水平。我们发现RSV对各组间的MMP-9、COX-1、COX-2或NF-κB mRNA水平没有显著影响。然而,与对照组相比,糖尿病组的SIRT1 mRNA水平降低,与糖尿病组相比,糖尿病+RSV组的SIRT1 mRNA水平升高。在糖尿病心脏组织中,RSV治疗可激活SIRT1。RSV激活SIRT1可能会为糖尿病心脏组织带来一种新的治疗方法。我们得出结论,RSV治疗可通过抑制如SIRT1等炎症基因的表达来缓解心脏功能障碍。

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