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豚鼠心肌细胞内向整流钾通道外向电流的复极化诱导短暂增加。

A repolarization-induced transient increase in the outward current of the inward rectifier K+ channel in guinea-pig cardiac myocytes.

作者信息

Ishihara K, Ehara T

机构信息

Department of Physiology, Saga Medical School, Saga 849-8501, Japan.

出版信息

J Physiol. 1998 Aug 1;510 ( Pt 3)(Pt 3):755-71. doi: 10.1111/j.1469-7793.1998.755bj.x.

Abstract
  1. Outward currents of the inwardly rectifying K+ current (IKir) in guinea-pig ventricular myocytes were studied in the presence of 1 mM intracellular free Mg2+ using the whole-cell patch-clamp technique. 2. During repolarizing voltage steps following a large depolarizing pulse (> 0 mV), outward IKir increased transiently at voltages positive to the K+ equilibrium potential (EK, -84 mV for 5.4 mM extracellular [K+]). The rising phase was almost instantaneous, while the decay was exponential. The decay rate was faster at voltages closer to EK (time constants, 33.9 +/- 9.8 and 4.8 +/- 1.4 ms at -30 and -50 mV, respectively). 3. The transient outward IKir was absent when the preceding depolarization was applied from -40 mV. Larger transient currents developed as the voltage before the depolarization was shifted to more hyperpolarized levels. 4. Shift of the depolarizing voltage from > 0 mV to more negative ranges diminished the amplitudes of transient outward IKir and instantaneous inward IKir during the subsequent repolarizing steps positive and negative to EK, respectively. Since blockage of IKir by internal Mg2+ occurs upon large depolarization, and the block is instantaneously relieved at voltages negative to EK, the rising phase of the transient outward IKir was attributed to the relief of Mg2+ block at voltages positive to EK. Transient outward IKir was absent when intracellular [Mg2+] was reduced to 10 microM or lower. 5. Prolongation of the repolarizing voltage step increased the amplitude of time-dependent inward IKir during the subsequent hyperpolarization, indicating the progress of a gating process (presumably the channel block by intracellular polyamine) during the decaying phase of outward IKir. 6. Progressive prolongation of the depolarizing pulse (> 0 mV) from 100 to 460 ms decreased the transient outward IKir amplitude during the subsequent repolarizing step due to slow progress of the gating (polyamine block) at > 0 mV. 7. Current-voltage relations measured using repolarizing ramp pulses (-3.4 mV ms-1) showed an outward hump at around -50 mV, the magnitude of which increased as the voltage before the conditioning depolarization (10 mV) was shifted to more negative levels. With slower ramp speeds (-1.5 and -0.6 mV ms-1), the hump was depressed at voltages near EK. 8. Our study suggests that the relief of Mg2+ block may increase outward IKir during repolarization of cardiac action potentials, and that the resting potential, the level/duration of action potential plateau and the speed of repolarization influence the outward IKir amplitude. 9. A kinetic model incorporating a competition between polyamine block and Mg2+ block was able to account for the time dependence of outward IKir.
摘要
  1. 采用全细胞膜片钳技术,在细胞内游离镁离子浓度为1 mM的条件下,研究豚鼠心室肌细胞内向整流钾电流(IKir)的外向电流。2. 在大的去极化脉冲(> 0 mV)后的复极化电压阶跃期间,外向IKir在高于钾离子平衡电位(EK,细胞外[K+]为5.4 mM时为-84 mV)的电压下短暂增加。上升阶段几乎是瞬间的,而衰减是指数性的。在更接近EK的电压下,衰减速率更快(时间常数在-30 mV和-50 mV时分别为33.9±9.8和4.8±1.4 ms)。3. 当从-40 mV施加先前的去极化时,不存在短暂外向IKir。随着去极化前的电压向更超极化水平移动,会产生更大的短暂电流。4. 将去极化电压从> 0 mV移至更负的范围,分别减小了随后在高于和低于EK的复极化步骤期间短暂外向IKir和瞬时内向IKir的幅度。由于细胞内镁离子在大的去极化时会阻断IKir,并且在低于EK的电压下阻断会瞬间解除,因此短暂外向IKir的上升阶段归因于在高于EK的电压下镁离子阻断的解除。当细胞内[Mg2+]降至10 μM或更低时,短暂外向IKir不存在。5. 复极化电压阶跃的延长增加了随后超极化期间时间依赖性内向IKir的幅度,表明在外向IKir的衰减阶段存在门控过程(可能是细胞内多胺对通道的阻断)的进展。6. 去极化脉冲(> 0 mV)从100 ms逐渐延长至460 ms,由于在> 0 mV时门控(多胺阻断)进展缓慢,导致随后复极化步骤期间短暂外向IKir幅度减小。7. 使用复极化斜坡脉冲(-3.4 mV/ms)测量的电流-电压关系在约-50 mV处显示出一个外向驼峰,其幅度随着条件性去极化(10 mV)前的电压向更负水平移动而增加。对于较慢的斜坡速度(-1.5和-0.6 mV/ms),在接近EK的电压下驼峰降低。8. 我们的研究表明,镁离子阻断的解除可能会在心脏动作电位复极化期间增加外向IKir,并且静息电位、动作电位平台期的水平/持续时间以及复极化速度会影响外向IKir幅度。9. 一个包含多胺阻断和镁离子阻断竞争的动力学模型能够解释外向IKir的时间依赖性。

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