Nargeot J, Mangoni M E
Institut de génomique fonctionnelle, UMR CNRS 5203 Inserm U 661, Universités de Montpellier I et II, France.
Arch Mal Coeur Vaiss. 2006 Sep;99(9):856-61.
The spontaneous activity (or pacemaker activity) of the heart constitutes a fundamental physiological function in higher organisms. Pacemaker activity is generated in the sino-atrial node (SAN) by a specialized cell population adapted to the generation of a rhythmic electrical oscillation. The precise ionic mechanisms underlying initiation of pacemaking in automatic cells has not been entirely elucidated. Ionic channels and intracellular Ca2+ signalling in pacemaker cells are both required for the proper setting of pacemaking. Understanding the mechanisms of pacemaker activity is important for developing new therapeutic approaches for controlling the heart rate in the diseased myocardium. Controlling the heart rate in the clinical practice is a promising way to increase cardioprotection and improve patient's survival in cardiac ischemic pathology. We describe here the contribution of several ion channels families into the generation and regulation of the heart rate using new approaches involving genetically modified mouse strains. These studies underline the functional redundancy of mechanisms underlying pacemaking, an important safety parameter for new drugs targeting ion channels to modulate cardiac frequency.
心脏的自发活动(或起搏活动)是高等生物的一项基本生理功能。起搏活动由窦房结(SAN)中一群专门适应产生节律性电振荡的细胞产生。自动细胞中起搏起始的确切离子机制尚未完全阐明。起搏细胞中的离子通道和细胞内Ca2+信号传导对于起搏的正确设定都是必需的。了解起搏活动的机制对于开发控制患病心肌心率的新治疗方法很重要。在临床实践中控制心率是增强心脏保护和改善心脏缺血性病变患者生存率的一种有前景的方法。我们在此使用涉及基因改造小鼠品系的新方法描述了几个离子通道家族对心率产生和调节的贡献。这些研究强调了起搏机制的功能冗余,这是针对离子通道调节心脏频率的新药的一个重要安全参数。