Integrated modeling and simulation of recruitment of myocardial perfusion and oxygen delivery in exercise

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of molecular and cellular cardiology Pub Date : 2024-05-14 DOI:10.1016/j.yjmcc.2024.05.006
Victoria E. Sturgess , Johnathan D. Tune , C. Alberto Figueroa , Brian E. Carlson , Daniel A. Beard
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Abstract

While exercise-mediated vasoregulation in the myocardium is understood to be governed by autonomic, myogenic, and metabolic-mediated mechanisms, we do not yet understand the spatial heterogeneity of vasodilation or its effects on microvascular flow patterns and oxygen delivery. This study uses a simulation and modeling approach to explore the mechanisms underlying the recruitment of myocardial perfusion and oxygen delivery in exercise. The simulation approach integrates model components representing: whole-body cardiovascular hemodynamics, cardiac mechanics and myocardial work; myocardial perfusion; and myocardial oxygen transport. Integrating these systems together, model simulations reveal: (1.) To match expected flow and transmural flow ratios at increasing levels of exercise, a greater degree of vasodilation must occur in the subendocardium compared to the subepicardium. (2.) Oxygen extraction and venous oxygenation are predicted to substantially decrease with increasing exercise level preferentially in the subendocardium, suggesting that an oxygen-dependent error signal driving metabolic mediated recruitment of flow would be operative only in the subendocardium. (3.) Under baseline physiological conditions approximately 4% of the oxygen delivered to the subendocardium may be supplied via retrograde flow from coronary veins.

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运动中心肌灌注和氧输送招募的综合建模和模拟。
据了解,运动介导的心肌血管调节受自主神经、肌源和代谢介导机制的支配,但我们还不了解血管扩张的空间异质性或其对微血管流动模式和氧输送的影响。本研究采用模拟和建模方法来探索运动中心肌灌注和氧输送的招募机制。模拟方法整合了代表以下方面的模型组件:全身心血管血流动力学、心脏力学和心肌功;心肌灌注;心肌氧输送。将这些系统集成在一起,模型模拟揭示了:(1)在运动量不断增加的情况下,要达到预期的血流量和透壁血流量比,心内膜下的血管扩张程度必须高于心外膜下。(2.) 随着运动量的增加,心内膜下的氧气萃取和静脉含氧量预计会大幅下降,这表明只有心内膜下才会出现氧气依赖性错误信号,驱动新陈代谢介导的血流招募。(3)在基线生理条件下,输送到心内膜下的氧气约有 4% 可能是通过冠状静脉逆流供应的。
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来源期刊
CiteScore
10.70
自引率
0.00%
发文量
171
审稿时长
42 days
期刊介绍: The Journal of Molecular and Cellular Cardiology publishes work advancing knowledge of the mechanisms responsible for both normal and diseased cardiovascular function. To this end papers are published in all relevant areas. These include (but are not limited to): structural biology; genetics; proteomics; morphology; stem cells; molecular biology; metabolism; biophysics; bioengineering; computational modeling and systems analysis; electrophysiology; pharmacology and physiology. Papers are encouraged with both basic and translational approaches. The journal is directed not only to basic scientists but also to clinical cardiologists who wish to follow the rapidly advancing frontiers of basic knowledge of the heart and circulation.
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Editorial Board PERM1 regulates mitochondrial energetics through O-GlcNAcylation in the heart Corrigendum to "PGE2 protects against heart failure through inhibiting TGF-β1 synthesis in cardiomyocytes and crosstalk between TGF-β1 and GRK2" [Journal of Molecular and Cellular Cardiology. 172(2022) 63-77]. Retraction notice to “The novel antibody fusion protein rhNRG1-HER3i promotes heart regeneration by enhancing NRG1-ERBB4 signaling pathway” [Journal of Molecular and Cellular Cardiology 187 (2023) 26–37] Exercise training attenuates cardiac dysfunction induced by excessive sympathetic activation through an AMPK-KLF4-FMO2 axis
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