[评估心肌梗塞后早期心脏康复的不同时间,并研究基于合成肽的药物疗法,以平衡线粒体动力学过程]。

Harefuah Pub Date : 2024-02-01
Rani Wainer Shlomo, Offir Ertracht, Ron Golan, Shaul Atar, Nir Qvit
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引用次数: 0

摘要

导言心血管疾病是全球死亡的主要原因。其最常见的表现形式是缺血性心脏病(IHD),如心肌梗塞(MI)。物理康复是治疗缺血性心脏病患者的常用方法。然而,何时开始物理康复最有效尚无定论。不过,建议尽早开始。人们对了解心肌缺血和心肌细胞线粒体动力学过程之间的关系越来越感兴趣。心肌梗死后线粒体失衡会加速心脏损伤。肽类药物是一种有效而安全的治疗选择。目的:研究心肌梗死后的康复和肽干预,评估开始体育锻炼的最佳时间和心肌梗死后的线粒体功能:背景:早期训练和肽治疗将保护心肌梗死后的心肌免受加速损伤:方法:将 60 只大鼠分为 6 组:六组大鼠将接受缺血再灌注(I/R)手术,先闭塞左前降支动脉(LAD)30分钟,然后进行再灌注。三组将在心肌梗死后的不同时间点(3、7 或 21 天)开始为期 8 周的中等强度运动训练。另一组将在再灌注前注射合成肽 5'。静坐组和假静坐组将作为对照组。结果将通过线粒体功能测试、超声心动图、血液炎症和生化指标、压力/容积循环、运动测试和组织学进行评估:结果:运动训练和线粒体治疗后心脏生理机能的改善将揭示心脏康复的最佳时机和心肌梗死后的线粒体损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[EVALUATION OF DIFFERENT TIMINGS OF EARLY CARDIAC REHABILITATION AFTER MYOCARDIAL INFARCTION AND EXAMINATION OF DRUG THERAPY BASED ON THE SYNTHESIZED PEPTIDE TO BALANCE THE MITOCHONDRIAL DYNAMICS PROCESSES].

Introduction: Cardiovascular diseases are the main cause of mortality in the world. Their most common expression is ischemic heart disease (IHD) such as myocardial infarction (MI). Physical rehabilitation is a common practice for IHD patients. Yet, there is no definition of when is the most effective time to start physical rehabilitation. However, it is recommended to start it as soon as possible. There is a growing interest in understanding the relationship between IHD and cardiomyocytes mitochondrial dynamics processes. Mitochondrial imbalance after MI accelerates cardiac damage. Peptide-based drugs are an effective and safe treatment option.

Aims: To examine rehabilitation and peptide intervention post-MI to assess optimal time to start a physical activity and mitochondrial function post-MI.

Background: Early training as well as peptide treatment will protect the cardiac muscle post-MI from accelerated damage.

Methods: Sixty rats will be divided into 6 groups: Six groups will undergo ischemia-reperfusion (I/R) surgery, by a 30 minute occlusion of their left anterior descending artery (LAD) followed by reperfusion. Three groups will start moderate-intensity exercise training for 8 weeks at different time-points post-MI (3, 7, or 21 days). Another group will be injected with synthetic peptide 5' pre-reperfusion. A sedentary group and a sham group will be used as controls. Results will be assessed by a mitochondrial function test, echocardiography, blood inflammatory and biochemical markers, pressure/volume loops, an exercise test and histology.

Results: Improvement of cardiac physiology following exercise training, and mitochondrial treatment will shed light on the preferred timing of cardiac rehabilitation and the mitochondrial damage post-MI.

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