Department of Medical Physiology, Division Heart & Lungs, University Medical Center Utrecht, Yalelaan 50, 3584 CM, Utrecht, Netherlands.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6369-6389. doi: 10.1007/s00210-024-03116-5. Epub 2024 Apr 29.
The functioning of the human heart relies on complex electrical and communication systems that coordinate cardiac contractions and sustain rhythmicity. One of the key players contributing to this intricate system is the K2.1 potassium ion channel, which is encoded by the KCNJ2 gene. K2.1 channels exhibit abundant expression in both ventricular myocytes and Purkinje fibers, exerting an important role in maintaining the balance of intracellular potassium ion levels within the heart. And by stabilizing the resting membrane potential and contributing to action potential repolarization, these channels have an important role in cardiac excitability also. Either gain- or loss-of-function mutations, but also acquired impairments of their function, are implicated in the pathogenesis of diverse types of cardiac arrhythmias. In this review, we aim to elucidate the system functions of K2.1 channels related to cellular electrical signaling, communication, and their contributions to cardiovascular disease. Based on this knowledge, we will discuss existing and new pharmacological avenues to modulate their function.
人类心脏的功能依赖于复杂的电和通讯系统,这些系统协调心脏收缩并维持节律性。在这个错综复杂的系统中,发挥关键作用的一个因素是 K2.1 钾离子通道,它由 KCNJ2 基因编码。K2.1 通道在心室肌细胞和浦肯野纤维中均有丰富的表达,对维持心脏细胞内钾离子水平的平衡具有重要作用。通过稳定静息膜电位并促进动作电位复极化,这些通道在心脏兴奋性方面也具有重要作用。无论是功能获得性突变还是功能丧失性突变,以及它们功能的获得性损害,都与多种类型的心律失常的发病机制有关。在这篇综述中,我们旨在阐明 K2.1 通道与细胞电信号、通讯相关的系统功能,以及它们对心血管疾病的贡献。基于这些知识,我们将讨论现有的和新的药理学途径来调节它们的功能。