Mangoni Matteo E, Nargeot Joël
Institute of Functional Genomics, Department of Physiology, Centre National de la Recherche Scientifique UMR5203, INSERM U661, University of Montpellier I and II, Montpellier, France.
Physiol Rev. 2008 Jul;88(3):919-82. doi: 10.1152/physrev.00018.2007.
The heart automaticity is a fundamental physiological function in higher organisms. The spontaneous activity is initiated by specialized populations of cardiac cells generating periodical electrical oscillations. The exact cascade of steps initiating the pacemaker cycle in automatic cells has not yet been entirely elucidated. Nevertheless, ion channels and intracellular Ca(2+) signaling are necessary for the proper setting of the pacemaker mechanism. Here, we review the current knowledge on the cellular mechanisms underlying the generation and regulation of cardiac automaticity. We discuss evidence on the functional role of different families of ion channels in cardiac pacemaking and review recent results obtained on genetically engineered mouse strains displaying dysfunction in heart automaticity. Beside ion channels, intracellular Ca(2+) release has been indicated as an important mechanism for promoting automaticity at rest as well as for acceleration of the heart rate under sympathetic nerve input. The potential links between the activity of ion channels and Ca(2+) release will be discussed with the aim to propose an integrated framework of the mechanism of automaticity.
心脏自律性是高等生物的一项基本生理功能。这种自发活动由产生周期性电振荡的特殊心肌细胞群启动。启动自律细胞起搏周期的确切步骤尚未完全阐明。然而,离子通道和细胞内Ca(2+)信号对于起搏器机制的正确设置是必需的。在此,我们综述了目前关于心脏自律性产生和调节的细胞机制的知识。我们讨论了不同离子通道家族在心脏起搏中的功能作用的证据,并回顾了在心脏自律性存在功能障碍的基因工程小鼠品系上获得的最新结果。除了离子通道,细胞内Ca(2+)释放已被表明是促进静息时自律性以及在交感神经输入下加速心率的重要机制。将讨论离子通道活性与Ca(2+)释放之间的潜在联系,旨在提出一个自律性机制的综合框架。