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Activation and inactivation of the bursting potassium channel from fused Torpedo synaptosomes.

机译:融合的鱼雷突触小体中破裂的钾通道的活化和失活。

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摘要

1. The voltage dependence of the bursting potassium channel in fused synaptosomes from Torpedo electric organ was studied in vitro, using the inside-out and the cell-attached configurations of the patch clamp technique. 2. The patch of membrane was held at various holding potentials (-140 to -50 mV) and then stepped to test potentials (-50 to +40 mV) for periods ranging from 5 to 300 ms. Each potential step was repeated 200-600 times. After subtraction of the capacitative transients and the leakage currents, an ensemble-averaged current was obtained. This ensemble current showed a marked activation upon depolarization, followed by an inactivation. 3. The activation of the bursting potassium channel is markedly dependent on the voltage step. Activation was detected at voltages positive to -50 mV. The peak of the ensemble current increases with the degree of depolarization, while the time to the peak decreases. With progressively larger depolarization, there is a shortening in the delay between the onset of the voltage step and the opening of the bursting potassium channels. 4. The inactivation phase of the ensemble current could be described adequately in most of the experiments, as a single exponential decay to a steady-state inactivation level. The time constant of inactivation was not markedly voltage dependent. 5. Single channel analysis of the inactivation reveals that it is due to a reduction in the number of channel openings and not due to changes in single channel current amplitude or channel mean open time along the pulse. 6. The holding potential has a marked effect on the peak amplitude of the ensemble current, indicating that hyperpolarization removes inactivation and depolarization induces it. The peak amplitude vs. voltage relation was fitted by the Boltzmann equation. The half-maximal inactivation was -105.2 +/- 5.8 mV (mean +/- S.E.M.), suggesting that at the resting potential a substantial fraction of the bursting potassium channels is in an inactivated state. 7. Two-pulse experiments show that the recovery from inactivation is a slow process which lasts well over 1 s. 8. High-frequency stimulation (20-66.7 Hz) by 5 ms pulses produces a progressive decline in the peak ensemble current amplitude. The decline is larger at higher stimulation frequencies.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.使用膜片钳技术的由内而外和细胞附着的结构,在体外研究了鱼雷电器官的融合突触体中破裂的钾通道的电压依赖性。 2.将膜片保持在各种保持电势(-140至-50 mV),然后步进测试电势(-50至+40 mV)5至300 ms。每个可能的步骤重复200-600次。在减去电容瞬变和漏电流之后,获得了整体平均电流。该合奏电流在去极化时显示出明显的活化,随后失活。 3.爆裂的钾离子通道的激活明显取决于电压阶跃。在至-50 mV的正电压下检测到激活。集成电流的峰值随去极化程度的增加而增加,而到达峰值的时间减少。随着越来越大的去极化,在电压阶跃的开始和破裂的钾通道的打开之间的延迟缩短。 4.在大多数实验中,可以将集合电流的失活阶段充分描述为单个指数衰减到稳态失活水平。灭活的时间常数与电压无关。 5.对失活的单通道分析表明,这是由于通道开口数量的减少,而不是由于沿脉冲的单通道电流幅度或通道平均打开时间的变化。 6.保持电势对整体电流的峰值幅度有显着影响,表明超极化消除了失活,而去极化则诱导了失活。峰值幅度与电压的关系通过玻耳兹曼方程拟合。最大半数灭活是-105.2 +/- 5.8 mV(平均+/- S.E.M.),这表明在静止电位下,大部分破裂的钾离子通道处于灭活状态。 7.两脉冲实验表明,从失活中恢复是一个缓慢的过程,持续时间超过1 s。 8. 5 ms脉冲的高频刺激(20-66.7 Hz)导致峰值合奏电流幅度逐渐减小。在较高的刺激频率下,下降幅度更大。(抽象截断为400字)

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