Elinder F, Arhem P
Nobel Institute for Neurophysiology, Karolinska Institutet, Stockholm, Sweden.
Biophys J. 1994 Jul;67(1):71-83. doi: 10.1016/S0006-3495(94)80456-4.
The action of gadolinium (Gd3+) on ion currents in myelinated axons of Xenopus laevis was investigated with the voltage clamp technique. The analysis revealed the following effects. (i) The potential-dependent parameters of both Na and K channels were shifted. The shift was equally large for activation, inactivation, and activation time constant curves (+9 mV for 100 microM Gd3+). The effects could be explained by screening of fixed surface charges at a density of -1.2 e nm-2. (ii) The rate of gating for both Na and K channels was reduced more than predicted from the shift. This effect could be quantified as a scaling (by a factor 3 and 5 respectively at 100 microM Gd3+) of the activation time constant curves. (iii) An activation- and inactivation-independent block of both Na and K channels, obeying 1:1 stoichiometry with a Kd value of about 70 microM potential-independent block of leakage current, obeying 1:2 stoichiometry with a Kd value of 600 microM. (iv) The analysis suggests separate binding sites for the effects, comprising high affinity modulatory and blocking sites on the channel proteins and low affinity receptors on phospholipids, associated with the effect on the leakage current.
采用电压钳技术研究了钆(Gd3+)对非洲爪蟾有髓轴突离子电流的作用。分析揭示了以下效应:(i)Na和K通道的电位依赖性参数发生了偏移。激活、失活和激活时间常数曲线的偏移幅度相同(100μM Gd3+时为+9 mV)。这些效应可以通过以-1.2 e nm-2的密度筛选固定表面电荷来解释。(ii)Na和K通道的门控速率降低幅度超过了根据偏移量预测的幅度。这种效应可以量化为激活时间常数曲线的缩放(100μM Gd3+时分别为3倍和5倍)。(iii)Na和K通道存在与激活和失活无关的阻滞,其化学计量比为1:1,解离常数(Kd)值约为70μM;漏电流存在与电位无关的阻滞,化学计量比为1:2,Kd值为600μM。(iv)分析表明这些效应存在不同的结合位点,包括通道蛋白上的高亲和力调节和阻滞位点以及磷脂上的低亲和力受体,后者与对漏电流的效应相关。