Schouten V J, ter Keurs H E
J Physiol. 1985 Mar;360:13-25. doi: 10.1113/jphysiol.1985.sp015601.
Intracellular action potentials and isometric force were measured from thin trabeculae of the right ventricle of rat heart. Characteristic for the action potential of rat myocardium is a short plateau and a slow final repolarization phase. We have studied the influence of ionic composition of the medium and of stimulation frequency on the slow phase of repolarization and its relation to peak force. The results confirmed a positive correlation between peak force and the duration of the slow phase of repolarization, as has been reported for other species. An increase of [Ca2+]o caused a shortening of the slow phase of repolarization when peak force was kept constant. In low [Na+]o peak force was increased and the slow phase of repolarization was shortened. Reperfusion with normal medium after a period in low [Na+]o induced a transient prolongation of the slow phase of repolarization and reduction of peak force. The transient lasted about 20 min. In the presence of the Ca2+ entry blocker nifedipine the action potential duration and peak force were reduced. Low [Na+]o caused less shortening of the slow phase of repolarization and a greater increase of peak force. The slow phase of repolarization was prolonged transiently following reperfusion at normal [Na+]o, but only during a few beats. These results are in agreement with the hypothesis that the slow phase of repolarization is due to an inward current generated by Na+-Ca2+ exchange, as latter mechanism is known to be sensitive to the intracellular and extracellular concentrations of both Na+ and Ca2+.
从大鼠心脏右心室的细小梁中测量细胞内动作电位和等长力。大鼠心肌动作电位的特征是有一个短的平台期和一个缓慢的终末复极化阶段。我们研究了培养基离子组成和刺激频率对复极化慢相的影响及其与峰值力的关系。结果证实了峰值力与复极化慢相持续时间之间存在正相关,这与其他物种的报道一致。当峰值力保持恒定时,细胞外[Ca2+]增加导致复极化慢相缩短。在低细胞外[Na+]时,峰值力增加,复极化慢相缩短。在低细胞外[Na+]环境中一段时间后再用正常培养基灌注,会导致复极化慢相短暂延长和峰值力降低。这种短暂现象持续约20分钟。在存在Ca2+内流阻滞剂硝苯地平的情况下,动作电位持续时间和峰值力降低。低细胞外[Na+]导致复极化慢相缩短较少,峰值力增加较大。在正常细胞外[Na+]灌注后,复极化慢相短暂延长,但仅在少数搏动期间。这些结果与以下假设一致,即复极化慢相是由Na+-Ca2+交换产生的内向电流引起的,因为已知后一种机制对细胞内和细胞外的Na+和Ca2+浓度敏感。