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4-氨基吡啶对结区膜钾通道的阻断及其在去极化时的部分解除。

Block of potassium channels of the nodal membrane by 4-aminopyridine and its partial removal on depolarization.

作者信息

Ulbricht W, Wagner H H

出版信息

Pflugers Arch. 1976 Nov 30;367(1):77-87. doi: 10.1007/BF00583659.

Abstract
  1. Voltage clamp experiments were done on single myelinated nerve fibres of the frog, Rana esculenta. 2. 53 muM 4-aminopyridine (4-AP) reduced IK to about one-fifth if tested with infrequent (1/min) and short (10 ms) depolarizing pulses; the onset time constant under these circumstances was ca. 160 s (14-15 degrees C). After prolonged treatment the effect was virtually irreversible. 3. At equilibrium with 4-AP, increasing the frequency of short pulses removed part of the block, the block removal accelerating with increasing pulse duration and frequency. 4. In 53 muM 4-AP unblocking of K channels during long (0.8 s) depolarizing pulses proceeded with a time constant, taur, of ca. 0.2 s. Restoration of block at the resting potential proceeded with a much larger time constant, tau'r, of ca. 1 min. 5. The stationary fraction, rinfinity, of K channels conducting in 53 muM 4-AP was 0.66, 0.41, and 0.24 at V = 120, 50, and 0 mV, respectively. 6. In a series of experiments with [4-AP] varying between 13.3 and 848 muM, taur decreased from 0.25 to 0.10 s (V = 130 mV, ca. 17 degrees C) while rinfinity followed the empirical relation 1/rinfinity = 1 + ct + cv exp(-0.77 EF/RT) with E = V - 70 mV. ct and cv are dimensionless quantities that increase with [4-AP] and reflect the voltage-independent and voltage-dependent component, respectively, of block. 7. Block of K channels and partial removal are also observed with inward IK at raised [K+]O. Removal proceeds on depolarization even if IK is additionally but temporarily suppressed by tetraethylammonium. Hence neither direction nor amplitude of IK but only the pulse potential seems to determine the extent of block for a given [4-AP].
摘要
  1. 对食用蛙(Rana esculenta)的单根有髓神经纤维进行了电压钳实验。2. 若用低频(1次/分钟)和短时长(10毫秒)的去极化脉冲进行测试,53微摩尔的4 - 氨基吡啶(4 - AP)可将钾离子电流(IK)降低至约五分之一;在这种情况下,起始时间常数约为160秒(14 - 15摄氏度)。长时间处理后,该效应几乎不可逆。3. 在与4 - AP达到平衡时,增加短脉冲的频率可去除部分阻滞,且阻滞去除随脉冲持续时间和频率的增加而加速。4. 在53微摩尔的4 - AP中,长时间(0.8秒)去极化脉冲期间钾通道的解阻滞过程的时间常数(taur)约为0.2秒。静息电位时阻滞的恢复过程的时间常数(tau'r)大得多,约为1分钟。5. 在53微摩尔的4 - AP中,钾通道传导的稳态分数(rinfinity)在V = 120、50和0毫伏时分别为0.66、0.41和0.24。6. 在一系列实验中,[4 - AP]在13.3至848微摩尔之间变化,taur从0.25秒降至0.10秒(V = 130毫伏,约17摄氏度),而rinfinity遵循经验关系式1/rinfinity = 1 + ct + cv exp(-0.77 EF/RT),其中E = V - 70毫伏。ct和cv是无量纲量,它们随[4 - AP]增加,分别反映阻滞的电压非依赖性和电压依赖性成分。7. 在升高的[K + ]O下,内向IK也会出现钾通道阻滞和部分去除。即使IK被四乙铵额外但暂时抑制,去极化时仍会发生去除。因此,对于给定的[4 - AP],似乎不是IK的方向或幅度,而只是脉冲电位决定了阻滞的程度。

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