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运动调节 microRNAs 以保护糖尿病心脏中的冠脉和心功能。

Exercise Regulates MicroRNAs to Preserve Coronary and Cardiac Function in the Diabetic Heart.

机构信息

Department of Physiology, School of Biomedical Sciences, HeartOtago, University of Otago, Dunedin, New Zealand (J.K.-S.L., E.S., M.W., N.G., R.K., D.O.S.).

Department of Cardiac Physiology, National Cerebral and Cardiovascular Center Research Institute, Suita, Osaka, Japan (J.T.P., H.T., C.-K.D., D.-Y.Z., M.-H.K.).

出版信息

Circ Res. 2020 Nov 6;127(11):1384-1400. doi: 10.1161/CIRCRESAHA.120.317604. Epub 2020 Sep 10.

Abstract

RATIONALE

Diabetic heart disease (DHD) is a debilitating manifestation of type 2 diabetes mellitus. Exercise has been proposed as a potential therapy for DHD, although the effectiveness of exercise in preventing or reversing the progression of DHD remains controversial. Cardiac function is critically dependent on the preservation of coronary vascular function.

OBJECTIVE

We aimed to elucidate the effectiveness and mechanisms by which exercise facilitates coronary and cardiac-protection during the onset and progression of DHD.

METHODS AND RESULTS

Diabetic db/db and nondiabetic mice, with or without underlying cardiac dysfunction (16 and 8 weeks old, respectively) were subjected to either moderate-intensity exercise or high-intensity exercise for 8 weeks. Subsequently, synchrotron microangiography, immunohistochemistry, Western blot, and real-time polymerase chain reaction were used to assess time-dependent changes in cardiac and coronary structure and function associated with diabetes mellitus and exercise and determine whether these changes reflect the observed changes in cardiac-enriched and vascular-enriched microRNAs (miRNAs). We show that, if exercise is initiated from 8 weeks of age, both moderate-intensity exercise and high-intensity exercise prevented the onset of coronary and cardiac dysfunction, apoptosis, fibrosis, microvascular rarefaction, and disruption of miRNA signaling, as seen in the nonexercised diabetic mice. Conversely, the cardiovascular benefits of moderate-intensity exercise were absent if the exercise was initiated after the diabetic mice had already established cardiac dysfunction (ie, from 16 weeks of age). The experimental silencing or upregulation of miRNA-126 activity suggests the mechanism underpinning the cardiovascular benefits of exercise were mediated, at least in part, through tissue-specific miRNAs.

CONCLUSIONS

Our findings provide the first experimental evidence for the critical importance of early exercise intervention in ameliorating the onset and progression of DHD. Our results also suggest that the beneficial effects of exercise are mediated through the normalization of cardiovascular-enriched miRNAs, which are dysregulated in DHD.

摘要

背景

糖尿病性心脏病(DHD)是 2 型糖尿病的一种衰弱表现。运动已被提议作为 DHD 的一种潜在治疗方法,尽管运动在预防或逆转 DHD 进展方面的有效性仍存在争议。心脏功能的发挥严重依赖于冠状动脉功能的维持。

目的

我们旨在阐明运动在 DHD 发病和进展过程中促进冠状动脉和心脏保护的有效性和机制。

方法和结果

糖尿病 db/db 小鼠和非糖尿病小鼠(分别为 16 周龄和 8 周龄,存在或不存在潜在的心功能障碍)分别接受中等强度运动或高强度运动 8 周。随后,使用同步辐射微血管造影术、免疫组织化学、Western blot 和实时聚合酶链反应评估与糖尿病相关的心脏和冠状动脉结构和功能的时变变化,以及这些变化是否反映了心脏和血管丰富的 microRNAs(miRNAs)的观察变化。我们表明,如果从 8 周龄开始运动,中等强度运动和高强度运动均可预防非运动性糖尿病小鼠的冠状动脉和心脏功能障碍、细胞凋亡、纤维化、微血管稀疏和 miRNA 信号中断的发生。相反,如果在糖尿病小鼠已经出现心脏功能障碍(即 16 周龄)后开始运动,则中等强度运动的心血管益处则不存在。实验性沉默或上调 miRNA-126 活性表明,运动的心血管益处的机制至少部分是通过组织特异性 miRNAs 介导的。

结论

我们的研究结果为早期运动干预改善 DHD 发病和进展的重要性提供了首个实验证据。我们的结果还表明,运动的有益作用是通过调节心血管丰富的 miRNAs 来介导的,这些 miRNAs 在 DHD 中失调。

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