Schwarz J R, Grigat G
Physiologisches Institut, Universitätskrankenhaus Eppendorf, Hamburg, F.R.G.
Epilepsia. 1989 May-Jun;30(3):286-94. doi: 10.1111/j.1528-1157.1989.tb05300.x.
Voltage clamp experiments were performed in single myelinated nerve fibers of the rat and the effects of phenytoin (PHT) and carbamazepine (CBZ) on the ionic membrane currents were studied. PHT and CBZ are almost selective blockers of Na channels. The main part of this inhibition is a potential-dependent block which can be removed by hyperpolarization. The dose-response curve of PHT was described as a first-order reaction with Kd = 37 microM; 100 microM CBZ was equally as effective 100 microM PHT. Both drugs shift the steady-state Na inactivation curve (h infinity (V] to more negative membrane potentials and decrease its steepness. PHT and CBZ have equimolar effects on the shift and decrease in steepness of h infinity (V). All of the drug-induced effects depend on drug concentration. Both drugs induce a slowing of recovery from Na inactivation. PHT has a stronger slowing effect than CBZ. From this ensues a frequency-dependent block, which is more pronounced in the presence of PHT than of CBZ. The effects of both drugs can be interpreted in the framework of the modulated receptor hypothesis.
在大鼠的单根有髓神经纤维上进行了电压钳实验,研究了苯妥英(PHT)和卡马西平(CBZ)对离子膜电流的影响。PHT和CBZ几乎是钠通道的选择性阻滞剂。这种抑制的主要部分是电压依赖性阻滞,可通过超极化消除。PHT的剂量反应曲线被描述为一级反应,解离常数(Kd)= 37微摩尔;100微摩尔的CBZ与100微摩尔的PHT效果相同。两种药物均使稳态钠失活曲线(h∞(V))向更负的膜电位移动,并降低其斜率。PHT和CBZ对h∞(V)的移动和斜率降低具有等摩尔效应。所有药物诱导的效应均取决于药物浓度。两种药物均导致钠失活恢复减慢。PHT的减慢作用比CBZ更强。由此产生频率依赖性阻滞,在PHT存在时比在CBZ存在时更明显。两种药物的作用均可在调制受体假说的框架内进行解释。