Mitochondria and oxidative stress in heart aging.

AGE Pub Date : 2016-08-01 Epub Date: 2016-07-24 DOI:10.1007/s11357-016-9933-y
Beatriz Martín-Fernández, Ricardo Gredilla
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引用次数: 121

Abstract

As average lifespan of humans increases in western countries, cardiac diseases become the first cause of death. Aging is among the most important risk factors that increase susceptibility for developing cardiovascular diseases. The heart has very aerobic metabolism, and is highly dependent on mitochondrial function, since mitochondria generate more than 90 % of the intracellular ATP consumed by cardiomyocytes. In the last few decades, several investigations have supported the relevance of mitochondria and oxidative stress both in heart aging and in the development of cardiac diseases such as heart failure, cardiac hypertrophy, and diabetic cardiomyopathy. In the current review, we compile different studies corroborating this role. Increased mitochondria DNA instability, impaired bioenergetic efficiency, enhanced apoptosis, and inflammation processes are some of the events related to mitochondria that occur in aging heart, leading to reduced cellular survival and cardiac dysfunction. Knowing the mitochondrial mechanisms involved in the aging process will provide a better understanding of them and allow finding approaches to more efficiently improve this process.

Abstract Image

线粒体和氧化应激在心脏老化中的作用。
在西方国家,随着人类平均寿命的延长,心脏病已成为人类死亡的首要原因。衰老是增加患心血管疾病易感性的最重要风险因素之一。心脏具有非常好的有氧代谢,并且高度依赖于线粒体功能,因为线粒体产生超过90%的心肌细胞消耗的细胞内ATP。在过去的几十年里,一些研究已经支持线粒体和氧化应激在心脏衰老和心脏疾病(如心力衰竭、心脏肥厚和糖尿病性心肌病)的发展中的相关性。在当前的综述中,我们收集了不同的研究来证实这一作用。线粒体DNA不稳定性增加、生物能量效率受损、细胞凋亡增强和炎症过程是发生在心脏衰老过程中与线粒体相关的一些事件,导致细胞存活减少和心功能障碍。了解衰老过程中涉及的线粒体机制将提供更好的理解,并允许找到更有效地改进这一过程的方法。
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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来源期刊
AGE
AGE 医学-老年医学
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