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运动犬前馈性交感神经介导的冠状动脉舒张的定量分析

Quantitative analysis of feedforward sympathetic coronary vasodilation in exercising dogs.

作者信息

Gorman M W, Tune J D, Richmond K N, Feigl E O

机构信息

Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle, Washington 98195-7290, USA.

出版信息

J Appl Physiol (1985). 2000 Nov;89(5):1903-11. doi: 10.1152/jappl.2000.89.5.1903.

Abstract

Recent experiments demonstrate that feedforward sympathetic beta-adrenoceptor coronary vasodilation occurs during exercise. The present study quantitatively examined the contributions of epinephrine and norepinephrine to exercise coronary hyperemia and tested the hypothesis that circulating epinephrine causes feedforward beta-receptor-mediated coronary dilation. Dogs (n = 10) were chronically instrumented with a circumflex coronary artery flow transducer and catheters in the aorta and coronary sinus. During strenuous treadmill exercise, myocardial oxygen consumption increased by approximately 3.9-fold, coronary blood flow increased by approximately 3.6-fold, and arterial plasma epinephrine concentration increased by approximately 2.4-fold over resting levels. At arterial concentrations matching those during strenuous exercise, epinephrine infused at rest (n = 6) produced modest increases (18%) in flow and myocardial oxygen consumption but no evidence of direct beta-adrenoceptor-mediated coronary vasodilation. Arterial norepinephrine concentration increased by approximately 5. 4-fold during exercise, and coronary venous norepinephrine was always higher than arterial, indicating norepinephrine release from cardiac sympathetic nerves. With the use of a mathematical model of cardiac capillary norepinephrine transport, these norepinephrine concentrations predict an average interstitial norepinephrine concentration of approximately 12 nM during strenuous exercise. Published dose-response data indicate that this norepinephrine concentration increases isolated coronary arteriolar conductance by approximately 67%, which can account for approximately 25% of the increase in flow observed during exercise. It is concluded that a significant portion of coronary exercise hyperemia ( approximately 25%) can be accounted for by direct feedforward beta-adrenoceptor coronary vascular effects of norepinephrine, with little effect from circulating epinephrine.

摘要

最近的实验表明,运动期间会出现前馈性交感β-肾上腺素能受体介导的冠状动脉舒张。本研究定量检测了肾上腺素和去甲肾上腺素对运动性冠状动脉充血的作用,并验证了循环肾上腺素引起前馈性β受体介导的冠状动脉舒张这一假说。对10只犬进行长期手术,在其冠状动脉回旋支安装流量传感器,并在主动脉和冠状窦插入导管。在剧烈的跑步机运动期间,心肌耗氧量增加约3.9倍,冠状动脉血流量增加约3.6倍,动脉血浆肾上腺素浓度比静息水平增加约2.4倍。在静息状态下输注肾上腺素(n = 6),使动脉浓度达到剧烈运动时的水平,结果血流量和心肌耗氧量有适度增加(18%),但未发现直接的β-肾上腺素能受体介导的冠状动脉舒张证据。运动期间动脉去甲肾上腺素浓度增加约5.4倍,冠状静脉去甲肾上腺素浓度始终高于动脉,表明有去甲肾上腺素从心脏交感神经释放。利用心脏毛细血管去甲肾上腺素转运的数学模型,这些去甲肾上腺素浓度预测在剧烈运动期间平均间质去甲肾上腺素浓度约为12 nM。已发表的剂量反应数据表明,这种去甲肾上腺素浓度可使离体冠状动脉小动脉传导率增加约67%,这可解释运动期间观察到的血流量增加的约25%。得出的结论是,冠状动脉运动性充血的很大一部分(约25%)可由去甲肾上腺素直接的前馈性β-肾上腺素能受体冠状动脉血管效应来解释,而循环肾上腺素的作用很小。

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