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Cardiac Metabolic Limitations Contribute to Diminished Performance of the Heart in Aging
Xin Gao1, Djordje G Jakovljevic2, Daniel A Beard1
1Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan.
Insights
Aging hearts show reduced energy production (ATP) and impaired function, similar to heart failure. This study models how lower creatine and phosphate impact heart energy and pumping ability in older women.
Area of Science:
- Cardiovascular Physiology
- Metabolic Biochemistry
- Computational Biology
Background:
- Aging reduces myocardial energetics, including creatine phosphate/ATP ratio, total creatine, and ATP.
- These changes mirror those in failing hearts, with reduced cardiac performance and power output.
- Both aging and heart failure diminish cardiac function compared to young, healthy individuals.
Purpose of the Study:
- To test if reduced cytoplasmic adenine nucleotide, creatine, and phosphate pools impair ATP synthesis in aging hearts.
- To determine how these metabolite reductions cause metabolic, energetic, and mechanical dysfunction with aging.
- To investigate the impact on myocardial metabolism and cardiac function in adult females.
Main Methods:
- Developed an age-structured population model for myocardial energetics.
- Modeled myocardial ATP, ADP, creatine phosphate, creatine, and inorganic phosphate concentrations.
- Predicted metabolite concentrations as functions of cardiac work and age in adult females.
Main Results:
- Model predictions support the hypotheses regarding aging and myocardial energetics.
- Results align with previous experimental observations on cardiac function and metabolism.
- Demonstrated that reduced metabolite pools impair ATP synthesis and cardiac mechanical function.
Conclusions:
- Aging impairs myocardial ATP synthesis capacity and cardiac mechanical pumping ability.
- Provides a theoretical and computational framework to study heart energetics and performance with aging.
- Highlights the critical role of creatine and phosphate pools in maintaining cardiac function throughout life.
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.
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