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Quantitative Analyses of Coronary Vascular and Cardiac Mechanics in Health and Disease: Open-loop (feed-forward) and feedback control of coronary blood flow during exercise cardiac pacing and pressure changes

机译:健康和疾病中冠状动脉和心脏力学的定量分析:运动心脏起搏和压力变化过程中冠状动脉血流的开环(前馈)和反馈控制

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摘要

A control system model was developed to analyze data on in vivo coronary blood flow regulation and to probe how different mechanisms work together to control coronary flow from rest to exercise, and under a variety of experimental conditions, including cardiac pacing and with changes in coronary arterial pressure (autoregulation). In the model coronary flow is determined by the combined action of a feedback pathway signal that is determined by the level of plasma ATP in coronary venous blood, an adrenergic open-loop (feed-forward) signal that increases with exercise, and a contribution of pressure-mediated myogenic control. The model was identified based on data from exercise experiments where myocardial oxygen extraction, coronary flow, cardiac interstitial norepinephrine concentration, and arterial and coronary venous plasma ATP concentrations were measured during control and during adrenergic and purinergic receptor blockade conditions. The identified model was used to quantify the relative contributions of open-loop and feedback pathways and to illustrate the degree of redundancy in the control of coronary flow. The results indicate that the adrenergic open-loop control component is responsible for most of the increase in coronary blood flow that occurs during high levels of exercise. However, the adenine nucleotide-mediated metabolic feedback control component is essential. The model was evaluated by predicting coronary flow in cardiac pacing and autoregulation experiments with reasonable fits to the data. The analysis shows that a model in which coronary venous plasma adenine nucleotides are a signal in local metabolic feedback control of coronary flow is consistent with the available data.
机译:开发了一个控制系统模型,以分析体内冠状动脉血流调节的数据,并探索在静息起搏和冠状动脉变化等多种实验条件下,不同机制如何共同控制从休息到运动的冠状动脉血流。压力(自动调节)。在该模型中,冠状动脉血流是由反馈通路信号(由冠状静脉血中血浆ATP的水平决定),肾上腺素开环(前馈)信号随运动而增加以及压力介导的肌源性控制。根据运动实验中的数据确定模型,在控制期间以及肾上腺素能和嘌呤能受体阻滞条件下,测量心肌氧提取,冠状动脉血流,间质去甲肾上腺素浓度以及动脉和冠状静脉血浆ATP浓度。所识别的模型用于量化开环和反馈通路的相对贡献,并说明控制冠状动脉血流的冗余度。结果表明,肾上腺素能开环控制成分是高水平运动期间冠状动脉血流量增加的主要原因。但是,腺嘌呤核苷酸介导的代谢反馈控制成分至关重要。通过预测心脏起搏和自动调节实验中的冠状动脉血流对模型进行评估,并合理拟合数据。分析表明,在冠状动脉血流的局部代谢反馈控制中,冠状静脉血浆腺嘌呤核苷酸是信号的模型与现有数据一致。

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