Huo Rong, Sheng Yue, Guo Wen-Ting, Dong De-Li
Channels (Austin). 2014;8(3):203-9. doi: 10.4161/chan.28972.
Transient outward K+ current (I(to)) plays a crucial role in the early phase of cardiac action potential repolarization. Kv4.3 K(+) channel is an important component of I(to). The function and expression of Kv4.3 K(+) channel decrease in variety of heart diseases, especially in heart hypertrophy/heart failure. Int his review, we summarized the changes of cardiac Kv4.3 K(+) channel in heart diseases and discussed the potential role of Kv4.3 K(+) channel in heart hypertrophy/heart failure. In heart hypertrophy/heart failure of mice and rats, down regulation of Kv4.3 K(+) channel leads to prolongation of action potential duration (APD), which is associated with increased Ca(2+), activation of calcineurin and heart hypertrophy/heart failure.However, in canine and human, Kv4.3 K(+) channel does not play a major role in setting cardiac APD. So, in addition to Kv4.3 K(+) channel/APD/Ca(2+) pathway, there exits another mechanism of Kv4.3 K(+) channel in heart hypertrophy and heart failure: downregulation of Kv4.3 K(+) channels leads to CaMKII dissociation from Kv4.3–CaMKII complex and subsequent activation of the dissociated CaMKII , which induces heart hypertrophy/heart failure. Upregulation of Kv4.3K(+) channel inhibits CaMKII activation and its related harmful consequences. We put forward a new point-of-view that Kv4.3 K(+) channel is involved in heart hypertrophy/heart failure independently of its electric function, and drugs inhibiting or upregulating Kv4.3 K(+) channel might be potentially harmful or beneficial to hearts through CaMKII.
瞬时外向钾电流(I(to))在心脏动作电位复极化的早期阶段起着至关重要的作用。Kv4.3钾通道是I(to)的重要组成部分。Kv4.3钾通道的功能和表达在多种心脏病中降低,尤其是在心脏肥大/心力衰竭中。在本综述中,我们总结了心脏病中心脏Kv4.3钾通道的变化,并讨论了Kv4.3钾通道在心脏肥大/心力衰竭中的潜在作用。在小鼠和大鼠的心脏肥大/心力衰竭中,Kv4.3钾通道的下调导致动作电位时程(APD)延长,这与细胞内钙浓度(Ca(2+))增加、钙调神经磷酸酶激活以及心脏肥大/心力衰竭有关。然而,在犬类和人类中,Kv4.3钾通道在设定心脏APD方面并不起主要作用。因此,除了Kv4.3钾通道/APD/Ca(2+)途径外,在心脏肥大和心力衰竭中还存在Kv4.3钾通道的另一种机制:Kv4.3钾通道的下调导致CaMKII从Kv4.3–CaMKII复合物中解离,随后解离的CaMKII被激活,从而诱导心脏肥大/心力衰竭。Kv4.3钾通道的上调抑制CaMKII激活及其相关的有害后果。我们提出了一个新的观点,即Kv4.3钾通道独立于其电功能参与心脏肥大/心力衰竭,抑制或上调Kv4.3钾通道的药物可能通过CaMKII对心脏产生潜在的有害或有益影响。