Varró A, Nánási P P, Lathrop D A
Department of Pharmacology & Cell Biophysics, University of Cincinnati College of Medicine, OH.
Cardioscience. 1991 Dec;2(4):233-43.
Action potentials and ionic currents were measured by patch-clamp in single right ventricular myocytes isolated enzymatically from rabbits and guinea pigs at room temperature. Based upon the shape of their action potentials, the rabbit myocytes were divided into two groups. In group 1 (n = 15), a prominent phase of initial rapid repolarization (phase 1) occurred following the upstroke of the action potential. Action potentials recorded in the second group (n = 9) did not have a noticeable phase 1. In group 1, voltage-clamp protocols revealed a transient outward current (Ito) activated upon depolarization from a holding potential of -50 mV to potentials positive to -20 mV. This outward current inactivated rapidly (tau = 50 ms) in a voltage-independent manner. The transient outward current was not apparent in group 2. In all the rabbit myocytes, the inward calcium current (ICa) was activated between -30 and -20 mV, with a peak at 0 mV. The inactivation kinetics of the inward calcium current were dependent on the voltage. In 4 out of 11 cells, inactivation was best described by a single exponential relation, and in the remaining 7 cells by a double exponential relation. The recovery of the inward calcium current from inactivation and the restitution of the duration of the action potential showed similar time-courses of 132 +/- 11.6 ms (n = 8) and 163.7 +/- 23.0 ms (n = 6), respectively. In all the rabbit myocytes the relation between current and voltage, established at the end of 400 ms command pulses, displayed a negative slope conductance. In rabbit myocytes, unlike those of guinea pig, pulses as long as 5 s revealed the delayed rectifier outward current to be weak or absent. Our results suggest that two populations of ventricular myocytes exist in the rabbit; neither has a prominent delayed rectifier, at least at room temperature, while one group has a transient outward current and the other does not. The major currents controlling the duration of the action potential at room temperature in myocytes from the right ventricle of the rabbit, therefore, are the inward calcium current and the inward rectifier potassium current (IK1).
在室温下,采用膜片钳技术对从兔和豚鼠体内酶解分离出的单个右心室肌细胞的动作电位和离子电流进行测量。根据动作电位的形态,将兔肌细胞分为两组。在第1组(n = 15)中,动作电位上升支之后出现明显的初始快速复极化相(第1相)。在第2组(n = 9)中记录到的动作电位没有明显的第1相。在第1组中,电压钳实验方案显示,从-50 mV的钳制电位去极化到-20 mV以上的电位时,可激活一个瞬时外向电流(Ito)。该外向电流以电压非依赖方式快速失活(时间常数τ = 50 ms)。第2组中未观察到明显的瞬时外向电流。在所有兔肌细胞中,内向钙电流(ICa)在-30 mV至-20 mV之间被激活,在0 mV时达到峰值。内向钙电流的失活动力学取决于电压。在11个细胞中的4个细胞中,失活情况用单指数关系描述最佳,其余7个细胞用双指数关系描述最佳。内向钙电流从失活状态的恢复以及动作电位持续时间的恢复分别显示出相似的时间进程,分别为132±11.6 ms(n = 8)和163.7±23.0 ms(n = 6)。在所有兔肌细胞中,在400 ms指令脉冲结束时建立的电流与电压关系呈现负斜率电导。与豚鼠肌细胞不同,在兔肌细胞中,长达5 s的脉冲显示延迟整流外向电流微弱或不存在。我们的结果表明,兔体内存在两种类型的心室肌细胞;至少在室温下,两者均无明显的延迟整流电流,而一组有瞬时外向电流,另一组没有。因此,在兔右心室肌细胞中,室温下控制动作电位持续时间的主要电流是内向钙电流和内向整流钾电流(IK1)。