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兔窦房结起搏电位的研究:电压钳条件下钾活性的测量。

A study of pace-maker potential in rabbit sino-atrial node: measurement of potassium activity under voltage-clamp conditions.

作者信息

Maylie J, Morad M, Weiss J

出版信息

J Physiol. 1981 Feb;311:161-78. doi: 10.1113/jphysiol.1981.sp013579.

Abstract
  1. A single sucrose-gap voltage-clamp technique was used to control the membrane potential and to measure current in rabbit sino-atrial (SA) strips. K+ activity in the extracellular space was simultaneously measured using K+-selective micro-electrodes. 2. Using double-barrelled K+ selective micro-electrodes it was possible to measure the time course of accumulation or depletion of K+ accompanying a single action potential without complications arising from mechanical or electrical artifacts. 3. K+ activity in the extracellular space increased during the action potential and then decreased to base-line levels during the diastolic depolarization phase. Single beat accumulations of 0.1-0.4 M could be measured. 4. The magnitude of accumulation or depletion of K+ depended upon the membrane potential such that K+ accumulated at potentials positive to -50 mV (K+ efflux greater than K+ uptake) and was depleted from the extracellular space at potentials negative to -50 mV (K+ efflux less than K+ uptake). 5. The rate of K+ depletion was fairly constant during the time course of a clamp step within the range of diastolic depolarization (-55 to -75 mV) even though the accompanying membrane current showed marked time-dependent kinetics. 6. The total membrane conductance measured during the time course of the diastolic depolarization or during the time course of activation of time-dependent 'pace-maker' current remained fairly constant or increased. 7. No reversal potential for the time-dependent 'pace-maker' current could be measured at EK in solutions containing 2.7, 5.4 and 8.1 mM-K+. 8. These results do not support the turn-off a K+ conductance as the primary mechanisms for the generation of the pace-maker potential in SA nodal tissue; rather the results are more consistent with the idea that activation of an inward current, with large positive equilibrium potential, is responsible for pace-making activity.
摘要
  1. 采用单蔗糖间隙电压钳技术来控制兔窦房(SA)条带的膜电位并测量电流。使用钾离子选择性微电极同时测量细胞外空间的钾离子活性。2. 使用双管钾离子选择性微电极能够测量单个动作电位伴随的钾离子积累或消耗的时间进程,而不会因机械或电伪迹产生并发症。3. 动作电位期间细胞外空间的钾离子活性增加,然后在舒张期去极化阶段降至基线水平。可以测量到单次搏动积累量为0.1 - 0.4 M。4. 钾离子积累或消耗的幅度取决于膜电位,使得钾离子在高于 -50 mV的电位时积累(钾离子外流大于钾离子摄取),而在低于 -50 mV的电位时从细胞外空间消耗(钾离子外流小于钾离子摄取)。5. 在舒张期去极化范围内(-55至 -75 mV)的钳制步骤过程中,钾离子消耗速率相当恒定,尽管伴随的膜电流显示出明显的时间依赖性动力学。6. 在舒张期去极化过程或时间依赖性“起搏”电流激活过程中测量的总膜电导保持相当恒定或增加。7. 在含有2.7、5.4和8.1 mM - 钾离子的溶液中,在EK处无法测量到时间依赖性“起搏”电流的反转电位。8. 这些结果不支持关闭钾离子电导作为窦房结组织中起搏电位产生的主要机制;相反,这些结果更符合这样一种观点,即具有大的正平衡电位的内向电流的激活负责起搏活动。

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