瘦素在大鼠离体心脏缺血再灌注后的抗缺血作用:心脏特异性miRNA的作用

IF 0.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
E. Polyakova, E. Mikhaylov, S. Minasian, M. Galagudza, E. Shlyakhto
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引用次数: 0

摘要

背景:瘦素是一种与肥胖相关的脂肪因子,与心脏缺血再灌注损伤(IRI)的保护作用有关。在本研究中,研究了瘦素对离体大鼠心肌IRI的浓度依赖性影响。此外,我们分析了心肌miRNA的表达,以研究它们在瘦素介导的心脏保护中的潜在作用。方法:在Langendorff灌流的大鼠心脏中,用两种浓度(1.0 nM和3.1 nM)的瘦素预处理60分钟,检测瘦素对IRI的影响。心脏用含有各自浓度的瘦素的缓冲液进行30分钟的全缺血和120分钟的再灌注。分析心功能和心律失常的发生率。用组织化学方法评估梗塞的大小。使用RT-PCR分析心室心肌中miRNA-144、-208a、-378和-499的表达。结果:与3.1 nM瘦素相比,向缓冲液中添加1.0 nM瘦素可发挥梗死限制作用,保护缺血后心室功能,并防止再灌注心律失常。心脏暴露于1.0 nM瘦素后,心肌miRNA-208a的表达降低,在用3.1 nM瘦素灌注的心脏中显著升高。结论:低剂量(1.0 nM)的瘦素急性给药对IRI具有心脏保护作用。这种作用与心肌miRNA-208a表达减少有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-Ischemic Effect of Leptin in the Isolated Rat Heart Subjected to Global Ischemia-Reperfusion: Role of Cardiac-Specific miRNAs
Background: Leptin is an obesity-associated adipokine that has been implicated in cardiac protection against ischemia-reperfusion injury (IRI). In this study, concentration-dependent effects of leptin on myocardial IRI were investigated in the isolated rat heart. In addition, we analyzed myocardial miRNAs expression in order to investigate their potential involvement in leptin-mediated cardioprotection. Methods: The effect of leptin on IRI was examined in Langendorff-perfused rat hearts preconditioned with two leptin concentrations (1.0 nM and 3.1 nM) for 60 min. The hearts were subjected to 30 min global ischemia and 120 min reperfusion with buffer containing leptin in the respective concentration. Heart function and arrhythmia incidence were analyzed. Infarct size was assessed histochemically. Expression of miRNA-144, -208a, -378, and -499 was analyzed in the ventricular myocardium using RT-PCR. Results: The addition of 1.0 nM leptin to the buffer exerted an infarct-limiting effect, preserved post-ischemic ventricular function, and prevented reperfusion arrhythmia compared to 3.1 nM leptin. Myocardial expression of miRNA-208a was decreased after heart exposure to 1.0 nM leptin and significantly elevated in the hearts perfused with leptin at 3.1 nM. Conclusion: Acute administration of leptin at low dose (1.0 nM) results in cardiac protection against IRI. This effect is associated with reduced myocardial expression of miRNA-208a.
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来源期刊
Cardiogenetics
Cardiogenetics CARDIAC & CARDIOVASCULAR SYSTEMS-
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26
审稿时长
11 weeks
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