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本文引用的文献

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ACTION POTENTIALS OF GUINEA PIG ATRIA UNDER CONDITIONS WHICH ALTER CONTRACTION.改变收缩情况下豚鼠心房的动作电位
Am J Physiol. 1964 Feb;206:270-82. doi: 10.1152/ajplegacy.1964.206.2.270.
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A study of intracellular potentials and contractions in atria, including evidence for an after-potential.一项关于心房细胞内电位与收缩的研究,包括后电位的证据。
J Physiol. 1959 Dec;149(1):78-92. doi: 10.1113/jphysiol.1959.sp006326.
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Activity-dependent changes of slow inward current in ventricular heart muscle.心室肌慢内向电流的活动依赖性变化。
Pflugers Arch. 1981 Oct;391(4):277-83. doi: 10.1007/BF00581507.
4
The electrogenic Na-Ca exchange and the cardiac electrical activity. I--Simulation on Purkinje fibre action potential.电致钠钙交换与心脏电活动。I——浦肯野纤维动作电位的模拟
J Physiol (Paris). 1981 Sep;77(6-7):705-9.
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Calcium transients in mammalian ventricular muscle.哺乳动物心室肌中的钙瞬变。
Eur Heart J. 1980;Suppl A:5-15. doi: 10.1093/eurheartj/1.suppl_1.5.
6
Frequency dependence of the ionic currents determining the action potential repolarization in rat ventricular muscle.决定大鼠心室肌动作电位复极化的离子电流的频率依赖性。
J Mol Cell Cardiol. 1981 Feb;13(2):207-15. doi: 10.1016/0022-2828(81)90217-0.
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Potential and tension changes induced by sodium removal in dog Purkinje fibres: role of an electrogenic sodium-calcium exchange.狗浦肯野纤维中钠去除所诱导的电位和张力变化:电致钠钙交换的作用
J Physiol. 1981 Feb;311:605-22. doi: 10.1113/jphysiol.1981.sp013607.
8
Membrane currents, contractions, and aftercontractions in cardiac Purkinje fibers.心脏浦肯野纤维中的膜电流、收缩及后收缩
Am J Physiol. 1982 Jul;243(1):H77-86. doi: 10.1152/ajpheart.1982.243.1.H77.
9
Analysis of the effects of changes in rate and rhythm upon electrical activity in the heart.心率和心律变化对心脏电活动影响的分析。
Prog Biophys Mol Biol. 1980;36(1):1-52. doi: 10.1016/0079-6107(81)90003-1.
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The cardiac excitation-contraction cycle.心脏兴奋-收缩周期。
Pharmacol Ther. 1982;16(1):1-43. doi: 10.1016/0163-7258(82)90030-4.

大鼠心脏动作电位的缓慢复极化阶段。

The slow repolarization phase of the action potential in rat heart.

作者信息

Schouten V J, ter Keurs H E

出版信息

J Physiol. 1985 Mar;360:13-25. doi: 10.1113/jphysiol.1985.sp015601.

DOI:10.1113/jphysiol.1985.sp015601
PMID:3989712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1193445/
Abstract

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+.

摘要

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。