交感神经系统对心脏钙通道的调节。

Q1 Pharmacology, Toxicology and Pharmaceutics
Pedro J Del Rivero Morfin, Steven O Marx, Manu Ben-Johny
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引用次数: 0

摘要

钙流入通过电压门控钙通道Cav1.2,在心肌细胞中启动心脏的兴奋-收缩耦合。心脏收缩的力度和速度由交感神经系统调节,主要由细胞内钙的变化介导。从支配心脏神经的交感神经元释放的去甲肾上腺素和由肾上腺染色质细胞分泌的肾上腺素结合到心肌细胞肌膜上的β-肾上腺素能受体,启动信号级联,产生cAMP并激活蛋白激酶a,其目标是控制钙的流入。几十年来,PKA调节心脏钙通道的机制尚不清楚。最近,这些机制已被阐明。在本章中,我们将回顾该领域的历史以及导致进化保守过程识别的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sympathetic Nervous System Regulation of Cardiac Calcium Channels.

Calcium influx through voltage-gated calcium channels, Cav1.2, in cardiomyocytes initiates excitation-contraction coupling in the heart. The force and rate of cardiac contraction are modulated by the sympathetic nervous system, mediated substantially by changes in intracellular calcium. Norepinephrine released from sympathetic neurons innervating the heart and epinephrine secreted by the adrenal chromaffin cells bind to β-adrenergic receptors on the sarcolemma of cardiomyocytes initiating a signaling cascade that generates cAMP and activates protein kinase A, the targets of which control calcium influx. For decades, the mechanisms by which PKA regulated calcium channels in the heart were not known. Recently, these mechanisms have been elucidated. In this chapter, we will review the history of the field and the studies that led to the identification of the evolutionarily conserved process.

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来源期刊
Handbook of experimental pharmacology
Handbook of experimental pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.20
自引率
0.00%
发文量
54
期刊介绍: The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.
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