毒蕈碱乙酰胆碱受体
窦房结
内科学
受体
毒蕈碱乙酰胆碱受体M2
毒蕈碱乙酰胆碱受体M3
内分泌学
刺激
医学
血管收缩
心率
血压
出处
期刊:Handbook of experimental pharmacology
日期:2011-11-03
卷期号:: 299-316
被引量:64
标识
DOI:10.1007/978-3-642-23274-9_13
摘要
Muscarinic receptor activation plays an essential role in parasympathetic regulation of cardiovascular function. The primary effect of parasympathetic stimulation is to decrease cardiac output by inhibiting heart rate. However, pharmacologically, muscarinic agonists are actually capable of producing both inhibitory and stimulatory effects on the heart as well as vasculature. This reflects the fact that muscarinic receptors are expressed throughout the cardiovascular system, even though they are not always involved in mediating parasympathetic responses. In the heart, in addition to regulating heart rate by altering the electrical activity of the sinoatrial node, activation of M2 receptors can affect conduction of electrical impulses through the atrioventricular node. These same receptors can also regulate the electrical and mechanical activity of the atria and ventricles. In the vasculature, activation of M3 and M5 receptors in epithelial cells can cause vasorelaxation, while activation of M1 or M3 receptors in vascular smooth muscle cells can cause vasoconstriction in the absence of endothelium. This review focuses on our current understanding of the signaling mechanisms involved in mediating these responses.
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