Mazzanti M, DeFelice L J
Biophys J. 1987 Jan;51(1):115-21. doi: 10.1016/S0006-3495(87)83316-7.
This paper describes the kinetics of an Na-conducting channel during spontaneous action potentials in beating heart cells and during simulated action potentials driven from the patch when the cell is not beating. Since the channel conducts Na only in Ca concentrations below 10(-6) M, and since it is insensitive to tetrodotoxin and has a conductance of 100 pS in 133 mM Na, we identify it as the Ca channel conducting Na in zero Ca. By comparing the channel in beating and nonbeating cells, but under conditions in which it experiences the same voltage in both cases, we observe that: open-channel conductance is the same in beating and nonbeating cells; the channel reversal potential is 25 mV in beating cells and 50 mV in nonbeating cells; the average current peaks later in beating cells than in nonbeating cells, and it has a different time course in the two cases that is not explained by the shift in reversal potential alone; and the average Na current through Ca channels in beating cells peaks much later during the action potential than we would expect if the channel were carrying Ca. We conclude that when the Ca channel conducts Na, its kinetics and reversal potential are strongly influenced by cytoplasmic factors that accompany beating, and that its behavior is not governed by voltage alone. We also conclude that when the Ca channel conducts Na, not only are its reversal potential and conductance altered from what they would be were the channel carrying Ca, but also the channel's kinetics depend on the permeant ion. Since only the channels in the patch are in zero Ca and are conducting Na, while the Ca channels surrounding the patch are in 1.5 mM Ca and are conducting Ca, our data support the idea that it is only the Ca passing through individual channels that influences the kinetics of those same channels.
本文描述了在跳动的心脏细胞自发动作电位期间以及在细胞不跳动时从膜片钳驱动的模拟动作电位期间,一种钠传导通道的动力学特性。由于该通道仅在钙浓度低于10^(-6) M时传导钠,且对河豚毒素不敏感,在133 mM钠中电导为100 pS,我们将其鉴定为在零钙条件下传导钠的钙通道。通过比较跳动和不跳动细胞中的通道,但在两种情况下通道经历相同电压的条件下,我们观察到:跳动和不跳动细胞中的开放通道电导相同;跳动细胞中的通道反转电位为25 mV,不跳动细胞中的为50 mV;跳动细胞中的平均电流峰值比不跳动细胞中的出现得晚,并且在两种情况下具有不同的时间进程,这不能仅由反转电位的变化来解释;跳动细胞中通过钙通道的平均钠电流在动作电位期间的峰值比如果该通道传导钙时我们预期的要晚得多。我们得出结论,当钙通道传导钠时,其动力学和反转电位受到伴随跳动的细胞质因素的强烈影响,并且其行为不仅仅由电压决定。我们还得出结论,当钙通道传导钠时,不仅其反转电位和电导与传导钙时不同,而且通道的动力学还取决于通透离子。由于只有膜片中的通道处于零钙并传导钠,而膜片周围的钙通道处于1.5 mM钙并传导钙,我们的数据支持这样一种观点,即只有通过单个通道的钙才会影响这些相同通道的动力学。