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心脏衰老过程中的代谢变化。

Metabolic Changes in Cardiac Aging.

作者信息

Hao Yan, Liu Wei

机构信息

Department of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, 150001 Harbin, Heilongjiang, China.

Department of Geriatric Cardiovascular Division, Guangdong Provincial Geriatrics Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, 510080 Guangzhou, Guangdong, China.

出版信息

Rev Cardiovasc Med. 2023 Mar 6;24(3):82. doi: 10.31083/j.rcm2403082. eCollection 2023 Mar.

DOI:10.31083/j.rcm2403082
PMID:39077479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11264006/
Abstract

Cardiac aging is a natural process accompanied by cardiomyocyte hypertrophy and dysfunction. These changes can lead to adverse organ remodeling and ultimately lead to the development of heart failure. The study of cardiac aging is helpful to explore the mechanism of senescence and is of great significance for preventing cardiac aging. Cardiac aging is accompanied by changes in various metabolic functions. In this process, due to the change of metabolic substrates and enzyme activities, oxidative stress response increases, and reactive oxygen species (ROS) increases, accompanied by mitochondrial dysfunction and gene expression changes, so related protein metabolism also changes. Hormone metabolism and autophagy are also involved in the process of cardiac aging. Based on these findings, changes in diet, caloric restriction, improvement of mitochondrial function and promotion of autophagy have been proven to have positive effects in delaying cardiac aging. This article reviews the metabolic changes involved in the process of cardiac aging from different aspects, and briefly reviews the measures to improve cardiac aging.

摘要

心脏衰老 是一个伴随着心肌细胞肥大和功能障碍的自然过程。这些变化会导致不良的器官重塑,并最终导致心力衰竭的发生。对心脏衰老的研究有助于探索衰老机制,对预防心脏衰老具有重要意义。心脏衰老伴随着各种代谢功能的变化。在此过程中,由于代谢底物和酶活性的改变,氧化应激反应增强,活性氧(ROS)增加,同时伴有线粒体功能障碍和基因表达变化,因此相关的蛋白质代谢也会发生改变。激素代谢和自噬也参与心脏衰老过程。基于这些发现,饮食改变、热量限制、改善线粒体功能和促进自噬已被证明在延缓心脏衰老方面具有积极作用。本文从不同方面综述了心脏衰老过程中涉及的代谢变化,并简要回顾了改善心脏衰老的措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2969/11264006/d623bb6c42ee/2153-8174-24-3-082-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2969/11264006/86d3e3f3b6a3/2153-8174-24-3-082-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2969/11264006/d623bb6c42ee/2153-8174-24-3-082-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2969/11264006/86d3e3f3b6a3/2153-8174-24-3-082-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2969/11264006/d623bb6c42ee/2153-8174-24-3-082-g2.jpg

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本文引用的文献

1
Genetic Deletion of Galectin-3 Exacerbates Age-Related Myocardial Hypertrophy and Fibrosis in Mice.半乳糖凝集素-3基因缺失加剧小鼠年龄相关性心肌肥厚和纤维化
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Caloric restriction-mimetics for the reduction of heart failure risk in aging heart: with consideration of gender-related differences.热量限制模拟物可降低衰老心脏心力衰竭风险:考虑到与性别相关的差异。
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Deficiency Promotes Cardiomyocyte Senescence by Modulating Ddit3-Mediated ER Stress.缺乏通过调节 Ddit3 介导的内质网应激促进心肌细胞衰老。
Genes (Basel). 2022 Apr 18;13(4):711. doi: 10.3390/genes13040711.
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Dynamic Mitochondrial Proteome Under Polyamines Treatment in Cardiac Aging.多胺处理下心脏衰老过程中的动态线粒体蛋白质组
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Pentacyclic triterpene oleanolic acid protects against cardiac aging through regulation of mitophagy and mitochondrial integrity.五环三萜齐墩果酸通过调控线粒体自噬和线粒体完整性保护心脏衰老。
Biochim Biophys Acta Mol Basis Dis. 2022 Jul 1;1868(7):166402. doi: 10.1016/j.bbadis.2022.166402. Epub 2022 Mar 26.
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HS protects from oxidative stress-driven ACE2 expression and cardiac aging.HS 可防止氧化应激驱动的 ACE2 表达和心脏衰老。
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