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兔窦房结心肌细胞持续起搏活动期间的离子电流。

Ionic currents during sustained pacemaker activity in rabbit sino-atrial myocytes.

作者信息

Zaza A, Micheletti M, Brioschi A, Rocchetti M

机构信息

Department of General Physiology and Biochemistry, University of Milano, Italy.

出版信息

J Physiol. 1997 Dec 15;505 ( Pt 3)(Pt 3):677-88. doi: 10.1111/j.1469-7793.1997.677ba.x.

Abstract
  1. The contribution of various ionic currents to diastolic depolarization (DD) in rabbit sinoatrial myocytes was evaluated by the action potential clamp technique. Individual currents were identified, during sustained pacemaking activity reproduced under voltage clamp conditions, according to their sensitivity to specific channel blockers. 2. The current sensitive to dihydropyridines (DHPs), blockers of L-type Ca2+ current (ICa,L), was small and outward during most of DD. Diastolic DHP-sensitive current was affected by changes in the driving force for K+, but it was insensitive to E-4031, which blocks the current termed IK,r; it was abolished by cell dialysis with a Ca2+ chelator. 3. The current sensitive to 2 mM Cs+ (ICs), a blocker of hyperpolarization-activated current (I(f)), was inward during the whole DD and it was substantially larger than the net inward current flowing during this phase. However, diastolic IK,r, identified in the same cells as the current sensitive to the blocker E-4031, exceeded ICs 2-fold. 4. These findings suggest that: (a) Ca2+ influx during the pacemaker cycle increases a K+ conductance, thus inverting the direction of the net current generated by L-type Ca2+ channel activity during DD; (b) the magnitude of I(f) would be adequate to account fully for DD; however, the coexistence of a larger IK,r suggests that other channels besides I(f) contribute inward current during this phase.
摘要
  1. 采用动作电位钳技术评估了多种离子电流对兔窦房结心肌细胞舒张期去极化(DD)的作用。在电压钳条件下重现的持续起搏活动期间,根据各电流对特定通道阻滞剂的敏感性来识别单个电流。2. 对二氢吡啶(DHP)敏感的电流,即L型Ca2+电流(ICa,L)的阻滞剂,在大部分DD期间较小且为外向电流。舒张期对DHP敏感的电流受K+驱动力变化的影响,但对阻断IK,r电流的E-4031不敏感;用Ca2+螯合剂进行细胞透析可消除该电流。3. 对2 mM Cs+(ICs)敏感的电流,即超极化激活电流(I(f))的阻滞剂,在整个DD期间为内向电流,且其幅度明显大于该阶段流动的内向净电流。然而,在同一细胞中识别出的舒张期IK,r,即对阻滞剂E-4031敏感的电流,比ICs大2倍。4. 这些发现表明:(a)起搏周期中的Ca2+内流增加了K+电导,从而在DD期间使L型Ca2+通道活动产生的净电流方向反转;(b)I(f)的幅度足以完全解释DD;然而,较大的IK,r的共存表明,除I(f)外,其他通道在此阶段也有内向电流贡献。

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