Suppr超能文献

大鼠缺血预处理的心脏保护作用涉及脂联素上调。

Cardioprotection of ischemic preconditioning in rats involves upregulating adiponectin.

作者信息

Wang Hui, Wu Wenjing, Duan Jun, Ma Ming, Kong Wei, Ke Yuannan, Li Gang, Zheng Jingang

机构信息

Department of Intensive Care UnitChina-Japan Friendship Hospital, Beijing, People's Republic of China.

Department of CardiologyChina-Japan Friendship Hospital, Beijing, People's Republic of China.

出版信息

J Mol Endocrinol. 2017 May;58(4):155-165. doi: 10.1530/JME-16-0163. Epub 2017 Feb 20.

Abstract

It has been reported that ischemic preconditioning (IPC) and adiponectin (APN) are cardioprotective in many cardiovascular disorders. However, whether APN mediates the effect of IPC on myocardial injury has not been elucidated. This study was conducted to investigate whether IPC affects myocardial ischemic injury by increasing APN expression. Male adult rats with cardiac knockdowns of APN and its receptors via intramyocardial small-interfering RNA injection were subjected to IPC and then myocardial infarction (MI) at 24 h after IPC. Globular APN (gAd) was injected at 10 min before MI. APN mRNA and protein levels in myocardium as well as the plasma APN concentration were markedly high at 6 and 12 h after IPC. IPC ameliorated myocardial injury as evidenced by improved cardiac functions and a reduced infarct size. Compared with the control MI group, rats in the IPC + MI group had elevated levels of left ventricular ejection fraction and fractional shortening and a smaller MI size ( < 0.05). However, the aforementioned protective effects were ameliorated in the absence of APN and APN receptors, followed by the inhibition of AMP-activated protein kinase (AMPK) phosphorylation, but reversed by gAd treatment in wild-type rats, and AMPK phosphorylation increased ( < 0.05). Overall, our results suggest that the cardioprotective effects of IPC are partially due to upregulation of APN and provide a further insight into IPC-mediated signaling effects.

摘要

据报道,缺血预处理(IPC)和脂联素(APN)在许多心血管疾病中具有心脏保护作用。然而,APN是否介导IPC对心肌损伤的作用尚未阐明。本研究旨在探讨IPC是否通过增加APN表达来影响心肌缺血损伤。通过心肌内注射小干扰RNA使APN及其受体在心脏中敲低的成年雄性大鼠接受IPC处理,然后在IPC后24小时进行心肌梗死(MI)。在MI前10分钟注射球形APN(gAd)。IPC后6小时和12小时,心肌中的APN mRNA和蛋白水平以及血浆APN浓度显著升高。IPC改善了心肌损伤,表现为心脏功能改善和梗死面积减小。与对照MI组相比,IPC + MI组大鼠的左心室射血分数和缩短分数水平升高,MI面积更小(<0.05)。然而,在缺乏APN和APN受体的情况下,上述保护作用减弱,随后AMP激活的蛋白激酶(AMPK)磷酸化受到抑制,但在野生型大鼠中gAd处理可使其逆转,且AMPK磷酸化增加(<0.05)。总体而言,我们的结果表明,IPC的心脏保护作用部分归因于APN的上调,并为IPC介导的信号传导效应提供了进一步的见解。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验