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Front Physiol. 2017 Nov 27;8:939. doi: 10.3389/fphys.2017.00939. eCollection 2017.
2
Impact of age on the association between cardiac high-energy phosphate metabolism and cardiac power in women.年龄对女性心脏高能磷酸代谢与心功能之间相关性的影响。
Heart. 2018 Jan;104(2):111-118. doi: 10.1136/heartjnl-2017-311275. Epub 2017 Jun 12.
3
Influence of metabolic dysfunction on cardiac mechanics in decompensated hypertrophy and heart failure.代谢功能障碍对失代偿性肥厚和心力衰竭时心脏力学的影响。
J Mol Cell Cardiol. 2016 May;94:162-175. doi: 10.1016/j.yjmcc.2016.04.003. Epub 2016 Apr 13.
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Feedback Regulation and Time Hierarchy of Oxidative Phosphorylation in Cardiac Mitochondria.心脏线粒体氧化磷酸化的反馈调节与时间层级
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Catalytic Coupling of Oxidative Phosphorylation, ATP Demand, and Reactive Oxygen Species Generation.氧化磷酸化、ATP需求与活性氧生成的催化偶联
Biophys J. 2016 Feb 23;110(4):962-71. doi: 10.1016/j.bpj.2015.09.036.
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Experimentally calibrated population of models predicts and explains intersubject variability in cardiac cellular electrophysiology.经实验校准的模型群体可预测和解释心脏细胞电生理学中的个体间变异性。
Proc Natl Acad Sci U S A. 2013 Jun 4;110(23):E2098-105. doi: 10.1073/pnas.1304382110. Epub 2013 May 20.

心脏代谢限制导致衰老中心脏功能下降。

Cardiac Metabolic Limitations Contribute to Diminished Performance of the Heart in Aging.

机构信息

Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan.

Cardiovascular Research Centre, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.

出版信息

Biophys J. 2019 Dec 17;117(12):2295-2302. doi: 10.1016/j.bpj.2019.06.026. Epub 2019 Jul 2.

DOI:10.1016/j.bpj.2019.06.026
PMID:31395314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6990148/
Abstract

Changes in the myocardial energetics associated with aging-reductions in creatine phosphate/ATP ratio, total creatine, and ATP-mirror changes observed in failing hearts compared to healthy controls. Similarly, both aging and heart failure are associated with significant reductions in cardiac performance and maximal left ventricular cardiac power output compared with young healthy individuals. Based on these observations, we hypothesize that reductions in the concentrations of cytoplasmic adenine nucleotide, creatine, and phosphate pools that occur with aging impair the myocardial capacity to synthesize ATP at physiological free energy levels and that the resulting changes to myocardial energetic status impair the mechanical pumping ability of the heart. The purpose of this study is to test these hypotheses using an age-structured population model for myocardial metabolism in the adult female population and to determine the potential impact of reductions in key myocardial metabolite pools in causing metabolic/energetic and cardiac mechanical dysfunction associated with aging. To test these hypotheses, we developed a population model for myocardial energetics to predict myocardial ATP, ADP, creatine phosphate, creatine, and inorganic phosphate concentrations as functions of cardiac work and age in the adult female population. Model predictions support our hypotheses and are consistent with previous experimental observations. The major findings provide a novel, to our knowledge, theoretical and computational framework for further probing complex relationships between the energetics and performance of the heart with aging.

摘要

与衰老相关的心肌能量变化——磷酸肌酸/ATP 比值、总肌酸和 ATP 减少,与健康对照组相比,心力衰竭时观察到类似的变化。同样,衰老和心力衰竭都与心脏功能显著降低以及与年轻健康个体相比,左心室最大心脏功率输出降低有关。基于这些观察结果,我们假设随着衰老,细胞质腺嘌呤核苷酸、肌酸和磷酸盐池的浓度降低会损害心肌在生理自由能水平下合成 ATP 的能力,而心肌能量状态的变化会损害心脏的机械泵功能。本研究的目的是使用成年女性人群的心肌代谢结构模型来检验这些假设,并确定关键心肌代谢物池减少对与衰老相关的代谢/能量和心脏机械功能障碍的潜在影响。为了检验这些假设,我们开发了一个心肌能量学的群体模型,以预测成年女性人群中心肌 ATP、ADP、磷酸肌酸、肌酸和无机磷酸盐浓度作为心脏工作和年龄的函数。模型预测支持我们的假设,与先前的实验观察结果一致。主要发现为进一步探究心脏能量与衰老之间的复杂关系提供了新颖的、据我们所知的理论和计算框架。