Golovko Vladimir, Gonotkov Mikhail, Lebedeva Elena
Laboratory of Heart Physiology, Institute of Physiology, Komi Science Center, The Urals Branch of the Russian Academy of Sciences, Syktyvkar, Russia
Laboratory of Heart Physiology, Institute of Physiology, Komi Science Center, The Urals Branch of the Russian Academy of Sciences, Syktyvkar, Russia.
Physiol Rep. 2015 Jul;3(7). doi: 10.14814/phy2.12447.
The physiological role of Ito has yet to be clarified. The goal of this study is to investigate the possible contribution of the transient outward current (Ito) on the generation of transmembrane action potentials (APs) and the sensitivity of mouse sinoauricular node (SAN) cells to a 4-aminopyridine (4AP) as Ito blocker. The electrophysiological identification of cells was performed in the sinoauricular node artery area (nstrips = 38) of the subendocardial surface using microelectrode technique. In this study, for the first time, it was observed that dependence duration of action potential at the level of 20% repolarization (APD20) level under a 4AP concentration in the pacemaker SAN and auricular cells corresponds to a curve predicted by Hill's equation. APD20 raised by 70% and spike duration of AP increased by 15-25%, when 4AP concentration was increased from 0.1 to 5.0 mmol/L. Auricular cells were found to be more sensitive to 4AP than true pacemaker cells. This was accompanied by a decrease in the upstroke velocity as compared to the control. Our data and previous findings in the literature lead us to hypothesize that the 4AP-sensitive current participates in the repolarization formation of pacemaker and auricular type cells. Thus, study concerning the inhibitory effects of lidocaine and TTX on APD20 can explain the phenomenon of the decrease in upstroke velocity, which, for the first time, was observed after exposure to 4AP. Duration of AP at the level of 20% repolarization (APD20) under a 4-AP concentration 0.5 mmol/L in the true pacemaker cells lengthen by 60-70% with a control.
Ito的生理作用尚未明确。本研究的目的是探讨瞬时外向电流(Ito)对跨膜动作电位(AP)产生的可能贡献,以及小鼠窦房结(SAN)细胞对作为Ito阻滞剂的4-氨基吡啶(4AP)的敏感性。使用微电极技术在心内膜下表面的窦房结动脉区域(n = 38)对细胞进行电生理鉴定。在本研究中,首次观察到在起搏器SAN和心房细胞中,4AP浓度下动作电位在20%复极化水平(APD20)的依赖持续时间符合希尔方程预测的曲线。当4AP浓度从0.1 mmol/L增加到5.0 mmol/L时,APD20升高70%,AP的峰持续时间增加15 - 25%。发现心房细胞比真正的起搏细胞对4AP更敏感。与对照相比,这伴随着上升速度的降低。我们的数据和文献中的先前发现使我们假设4AP敏感电流参与起搏细胞和心房型细胞的复极化形成。因此,关于利多卡因和TTX对APD20抑制作用的研究可以解释首次在暴露于4AP后观察到的上升速度降低现象。在真正的起搏细胞中,0.5 mmol/L的4-AP浓度下,20%复极化水平(APD20)的AP持续时间比对照延长60 - 70%。