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miR-503 通过 Nrf2/ARE 信号通路参与了二期酶诱导剂(CPDT)在糖尿病心肌病中的保护作用。

miR-503 Is Involved in the Protective Effect of Phase II Enzyme Inducer (CPDT) in Diabetic Cardiomyopathy via Nrf2/ARE Signaling Pathway.

机构信息

Department of Endocrinology, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.

出版信息

Biomed Res Int. 2017;2017:9167450. doi: 10.1155/2017/9167450. Epub 2017 Dec 18.

Abstract

Diabetic cardiomyopathy (DCM) is a common heart disease. The Phase II enzyme inducer (CPDT) is a complex enzyme that promotes the expression of antioxidant enzymes through activating nuclear factor erythroid 2-related factor 2 (Nrf2); these compounds have been shown to protect against oxidative stress. However, whether these compounds have similar protective effects in DCM still remains unclear. The purpose of this study is to investigate the protective effects and potential mechanism of CPDT in diabetic cardiomyopathy. In the results, firstly, compared with control rats, myocardial cell size, left ventricular mass index, and myocardial apoptosis index were increased, miR-503 was increased, and Nrf2, malondialdehyde (MDA), and heme oxygenase 1 (HO-1) were decreased in diabetic cardiomyopathy rats. Furthermore, compared with diabetic cardiomyopathy rats, these above parameters show the opposite change in CPDT treatment rats. In addition, the bioinformatics and luciferase reporter assay demonstrated that Nrf2 is a direct target of miR-503. Finally, the miR-503 could also regulate Nrf2 in the myocardial cells. Therefore, miR-503 is involved in the protective effect of CPDT in diabetic cardiomyopathy via Nrf2/ARE signaling pathway; miR-503 and Nrf2 may be a promising therapeutic target for the management of diabetic cardiomyopathy.

摘要

糖尿病心肌病(DCM)是一种常见的心脏病。二期酶诱导剂(CPDT)是一种复杂的酶,通过激活核因子红细胞 2 相关因子 2(Nrf2)促进抗氧化酶的表达;这些化合物已被证明可抵抗氧化应激。然而,这些化合物在 DCM 中是否具有类似的保护作用尚不清楚。本研究旨在探讨 CPDT 在糖尿病心肌病中的保护作用及潜在机制。结果显示,与对照组大鼠相比,糖尿病心肌病大鼠的心肌细胞大小、左心室质量指数和心肌细胞凋亡指数增加,miR-503 增加,Nrf2、丙二醛(MDA)和血红素加氧酶 1(HO-1)减少;与糖尿病心肌病大鼠相比,CPDT 治疗大鼠的上述参数呈相反变化。此外,生物信息学和荧光素酶报告基因检测表明,Nrf2 是 miR-503 的直接靶标。最后,miR-503 还可以调节心肌细胞中的 Nrf2。因此,miR-503 通过 Nrf2/ARE 信号通路参与 CPDT 对糖尿病心肌病的保护作用;miR-503 和 Nrf2 可能是治疗糖尿病心肌病的有前途的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1600/5748299/fcf18f416dd4/BMRI2017-9167450.001.jpg

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