Araque A, Buño W
Instituto Cajal, CSIC, Madrid, Spain.
J Neurosci. 1994 Jan;14(1):399-408. doi: 10.1523/JNEUROSCI.14-01-00399.1994.
The ionic current underlying anomalous rectification in opener muscle fibers of crayfish was studied under two-electrode voltage clamp. Opener muscle fibers showed a mean resting potential (RP) of -64.8 mV and an input resistance of 0.4 M omega. Hyperpolarizing voltage command pulses from a holding potential (H) of -60 mV evoked an instantaneous voltage-independent linear current (IL) followed by a time- and voltage-dependent inward current (IAB) that reached a steady state within 500 msec. The reversal potential of IAB (EAB) was estimated from tail current amplitudes. At an extracellular K+ concentration ([K+]o) of 5.4 mm the mean EAB was -61.8 mV. EAB shifted toward positive potentials by 50.8 mV for a 10-fold increase in [K+]o. The conductance underlying IAB (GAB) increased sigmoidally with hyperpolarization, starting close to the RP, saturating at a GAB,max of about -140 mV, and showing a mean half-activation at -94.4 mV. The activation curve of GAB shifted 53.6 mV toward positive potentials with a 10-fold increase in [K+]o. GAB,max did not increase in raised [K+]o. The activation and deactivation kinetics of IAB were accurately described by single exponentials with similar time constants (< 100 msec). Time constants changed as an exponential function of the membrane potential. IAB, its time course, GAB, and EAB were not modified in the following conditions: (1) Na(+)- and Ca(2+)-free solutions, (2) intracellular EGTA, (3) extracellular (100 mM) or intracellular tetraethylammonium, (4) extracellular Cs+ (up to 50 mM), Rb+ (up to 10 mM), Ba2+ (13.5 mM), or Mn2+ (13.5 mM). However, low extracellular concentrations of Cd2+ or Zn2+ strongly and reversibly reduced both IL and IAB. Therefore, we conclude that anomalous rectification in crayfish muscle is generated by a voltage- and time-dependent K+ current IAB. This current displayed many electrophysiological and pharmacological characteristics that distinguished it from all others mediating anomalous rectification described previously.
在双电极电压钳制下,研究了小龙虾开肌纤维中反常整流的离子电流。开肌纤维的平均静息电位(RP)为-64.8 mV,输入电阻为0.4 MΩ。从-60 mV的钳制电位(H)施加超极化电压指令脉冲,会诱发一个瞬时电压无关的线性电流(IL),随后是一个时间和电压依赖性的内向电流(IAB),该电流在500毫秒内达到稳态。IAB的反转电位(EAB)通过尾电流幅度进行估计。在细胞外K⁺浓度([K⁺]o)为5.4 mM时,平均EAB为-61.8 mV。当[K⁺]o增加10倍时,EAB向正电位移动50.8 mV。IAB的电导(GAB)随着超极化呈S形增加,从接近RP处开始,在约-140 mV的GAB,max处达到饱和,平均半激活电位为-94.4 mV。当[K⁺]o增加10倍时,GAB的激活曲线向正电位移动53.6 mV。在升高的[K⁺]o中,GAB,max没有增加。IAB的激活和失活动力学可以用具有相似时间常数(<100毫秒)的单指数准确描述。时间常数随膜电位呈指数函数变化。在以下条件下,IAB及其时间进程、GAB和EAB未发生改变:(1)无Na⁺和Ca²⁺的溶液;(2)细胞内EGTA;(3)细胞外(100 mM)或细胞内四乙铵;(4)细胞外Cs⁺(高达50 mM)、Rb⁺(高达10 mM)、Ba²⁺(13.5 mM)或Mn²⁺(13.5 mM)。然而,低细胞外浓度的Cd²⁺或Zn²⁺会强烈且可逆地降低IL和IAB。因此,我们得出结论,小龙虾肌肉中的反常整流是由电压和时间依赖性的K⁺电流IAB产生的。该电流表现出许多电生理和药理学特征,使其与先前描述的所有其他介导反常整流的电流区分开来。