首页> 美国卫生研究院文献>The Journal of Physiology >Single sodium channels from canine ventricular myocytes: voltage dependence and relative rates of activation and inactivation.
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Single sodium channels from canine ventricular myocytes: voltage dependence and relative rates of activation and inactivation.

机译:犬心室肌细胞的单个钠通道:电压依赖性以及相对活化和失活速率。

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摘要

1. Single sodium channel currents were recorded from canine ventricular myocytes in cell-attached patches. The relative rates of single-channel activation vs. inactivation as well as the voltage dependence of the rate of open-channel inactivation were studied. 2. Ensemble-averaged sodium currents showed relatively normal activation and inactivation kinetics, although the mid-point of the steady-state inactivation (h infinity) curve was shifted by 20-30 mV in the hyperpolarizing direction. This shift was due to the bath solution, which contained isotonic KCl to depolarize the cell to 0 mV. 3. Steady-state activation showed less of a voltage shift. The threshold for eliciting channel opening was around -70 mV and the mid-point of activation occurred near -50 mV. 4. The decline of the ensemble-averaged sodium current during a maintained depolarization was fitted by a single exponential function characterizing the apparent time constant of inactivation (tau h). The apparent rate of inactivation was voltage dependent, with tau h decreasing e-fold for a 15.4 mV depolarization. 5. The relative contributions of the rates of single-channel activation and inactivation in determining the time course of current decay (tau h) were examined using the approach of Aldrich, Corey & Stevens (1983). Mean channel open time (tau o) showed significant voltage dependence, increasing from 0.5 ms at -70 mV to around 0.8 ms at -40 mV. At -70 mV tau h was much greater than tau o, while at -40 mV the two time constants were similar. 6. The degree to which the kinetics of single-channel activation contribute to tau h was studied using the first latency distribution. The first latency function was fitted by two exponentials. The slow component was voltage dependent, decreasing from 19 ms at -70 mV to 0.5 ms at -40 mV. The fast component (0.1-0.5 ms) was not well resolved. 7. Comparing the first latency distribution with the time course of the ensemble-averaged sodium current at -40 mV showed that activation is nearly complete by the time of peak inward sodium current. However, at -70 mV, activation overlaps significantly with the apparent time course of inactivation of the ensemble-averaged current. 8. Using the methods of Aldrich et al. (1983) we also measured the apparent rate of open-channel closing (a) and open-channel inactivation (b). Both rates were voltage dependent, with a showing an e-fold decrease for an 11 mV depolarization and b showing an e-fold increase for a 30 mV depolarization.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.在附着细胞的贴片中从犬心室肌细胞中记录到单个钠通道电流。研究了单通道激活相对于失活的相对速率,以及明通道失活速率的电压依赖性。 2.集合平均钠电流显示出相对正常的活化和失活动力学,尽管稳态失活(h无穷大)曲线的中点在超极化方向上偏移了20-30 mV。该变化是由于浴液所致,该溶液含有等渗的KCl,可将细胞去极化至0 mV。 3.稳态激活显示较少的电压漂移。引发通道开放的阈值约为-70 mV,激活的中点发生在-50 mV附近。 4.维持去极化过程中整体平均钠电流的下降通过表征失活的表观时间常数(tau h)的单个指数函数拟合。失活的表观速率与电压有关,tau降低了15.4 mV去极化的e倍。 5.使用Aldrich,Corey&Stevens(1983)的方法检验了单通道激活和失活速率在确定电流衰减的时间过程(tau h)中的相对贡献。平均通道断开时间(tau)显示出显着的电压依赖性,从-70 mV的0.5 ms增加到-40 mV的0.8 ms左右。在-70 mV时,tau h远大于tau o,而在-40 mV时,两个时间常数相似。 6.使用第一潜伏期分布研究了单通道激活动力学对tau h的贡献程度。第一个等待时间函数由两个指数拟合。慢速分量取决于电压,从-70 mV的19 ms降低到-40 mV的0.5 ms。快速分量(0.1-0.5毫秒)无法很好地解决。 7.将第一个潜伏期分布与整体平均钠电流在-40 mV的时间过程进行比较,结果表明,到钠内向电流峰值时,激活几乎已完成。但是,在-70 mV时,激活与整体平均电流的失活的表观时间过程明显重叠。 8.使用Aldrich等人的方法。 (1983)我们还测量了明渠关闭(a)和明渠灭活(b)的表观速率。两种速率均取决于电压,a表示去极化11 mV时e倍降低,b表示30 mV去极化b时e倍增加(摘要截短为400字)。

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