代谢性心脏病、衰老和心力衰竭中心脏线粒体健康与心肌结构重塑之间的动态相互作用。

The journal of cardiovascular aging Pub Date : 2023-01-01 Epub Date: 2023-01-03 DOI:10.20517/jca.2022.42
Benjamin Werbner, Omid Mohammad Tavakoli-Rouzbehani, Amir Nima Fatahian, Sihem Boudina
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引用次数: 0

摘要

这篇综述从整体角度探讨了代谢性心脏病、自然心脏衰老和心力衰竭背景下心脏线粒体功能障碍与心肌结构重塑之间的双向关系。首先,综述了心脏线粒体功能障碍在代谢综合征和心脏衰老等一系列日益普遍的疾病中的生理和分子驱动因素,然后对心脏线粒体质量控制(QC)机制进行了总体回顾。文章讨论了心脏线粒体功能障碍引发或导致心脏结构重塑的几种重要机制:累积的代谢副产物、氧化损伤、线粒体质量控制受损以及线粒体介导的细胞死亡,这些已被确定为肥厚和心肌纤维化等心脏结构重塑的重要机制因素。随后,我们探讨了研究较少但却非常重要的反向关系:心脏结构重塑反馈进一步改变线粒体生物能功能的机制。然后,我们简要介绍了几种日益重要的临床病症的发病机理,这些病症的核心就是这些关系:糖尿病心肌病、与年龄相关的心脏功能衰退以及心力衰竭的进展(无论是否有射血分数保留)。最后,我们确定了针对这些病症的线粒体功能的治疗机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The dynamic interplay between cardiac mitochondrial health and myocardial structural remodeling in metabolic heart disease, aging, and heart failure.

This review provides a holistic perspective on the bi-directional relationship between cardiac mitochondrial dysfunction and myocardial structural remodeling in the context of metabolic heart disease, natural cardiac aging, and heart failure. First, a review of the physiologic and molecular drivers of cardiac mitochondrial dysfunction across a range of increasingly prevalent conditions such as metabolic syndrome and cardiac aging is presented, followed by a general review of the mechanisms of mitochondrial quality control (QC) in the heart. Several important mechanisms by which cardiac mitochondrial dysfunction triggers or contributes to structural remodeling of the heart are discussed: accumulated metabolic byproducts, oxidative damage, impaired mitochondrial QC, and mitochondrial-mediated cell death identified as substantial mechanistic contributors to cardiac structural remodeling such as hypertrophy and myocardial fibrosis. Subsequently, the less studied but nevertheless important reverse relationship is explored: the mechanisms by which cardiac structural remodeling feeds back to further alter mitochondrial bioenergetic function. We then provide a condensed pathogenesis of several increasingly important clinical conditions in which these relationships are central: diabetic cardiomyopathy, age-associated declines in cardiac function, and the progression to heart failure, with or without preserved ejection fraction. Finally, we identify promising therapeutic opportunities targeting mitochondrial function in these conditions.

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