Benoit E, Escande D
Laboratoire de Physiologie comparée, URA CNRS 1121, Université Paris Sud, Orsay, France.
Pflugers Arch. 1991 Dec;419(6):603-9. doi: 10.1007/BF00370302.
The effects of 0.15-250 microM riluzole, a novel psychotropic agent with anticonvulsant properties, were studied on voltage-clamped nodes of Ranvier of isolated nerve fibres of the frog. When added to the external solution, the drug rapidly and reversibly inhibited both K and Na currents with an apparent dissociation constant of 0.09 mM. The riluzole-induced decrease of these currents was not "use-dependent". At concentrations up to 100 microM, the drug had no noticeable effect on the time course of Na current inactivation nor on the shape and the position along voltage axis of the Na conductance/voltage relationship. On the other hand, it induced substantial shifts towards negative voltages of the steady-state Na inactivation/voltage curve. From these results, according to the modulated-receptor model, an apparent dissociation constant of 0.29 microM could be calculated for riluzole-induced blockage of inactivated Na channels. The recovery from Na current inactivation was also affected by the drug. It is concluded that riluzole is a highly specific blocker of inactivated Na channels, which is more than 300 times more effective on these channels than on K or resting Na channels.
研究了新型抗惊厥精神药物利鲁唑(0.15 - 250微摩尔)对青蛙离体神经纤维郎飞结电压钳制的影响。当将该药物添加到外部溶液中时,它能快速且可逆地抑制钾电流和钠电流,其表观解离常数为0.09毫摩尔。利鲁唑引起的这些电流降低并非“使用依赖性”。在浓度高达100微摩尔时,该药物对钠电流失活的时间进程以及钠电导/电压关系曲线的形状和沿电压轴的位置均无明显影响。另一方面,它使稳态钠失活/电压曲线显著向负电压方向移动。根据这些结果,按照调制受体模型,可计算出利鲁唑诱导失活钠通道阻断的表观解离常数为0.29微摩尔。钠电流失活的恢复也受到该药物的影响。得出的结论是,利鲁唑是失活钠通道的高度特异性阻滞剂,它对这些通道的作用比对钾通道或静息钠通道的作用有效300倍以上。