Tas P W, Kress H G, Koschel K
FEBS Lett. 1985 Mar 25;182(2):269-72. doi: 10.1016/0014-5793(85)80313-6.
We have investigated the effect of pharmacological agents on [14C]guanidinium ion influx through sodium channels in C6 rat glioma and N18 mouse neuroblastoma cells. The sodium channels of the N18 cells can be activated by aconitine alone, indicating that they are voltage-dependent channels. In contrast, sodium channels in the C6 cells require the synergistic action of aconitine and scorpion toxin for activation and are therefore characterized as so-called silent channels. The general anesthetic halothane used at clinical concentrations, specifically inhibited the ion flux through the silent sodium channel of C6 rat glioma cells. The voltage-dependent channels of the N18 cells were insensitive to halothane at the concentrations tested.
我们研究了药物制剂对[14C]胍离子通过C6大鼠胶质瘤细胞和N18小鼠神经母细胞瘤细胞中钠通道内流的影响。N18细胞的钠通道仅可被乌头碱激活,这表明它们是电压依赖性通道。相比之下,C6细胞中的钠通道需要乌头碱和蝎毒素的协同作用才能激活,因此被称为所谓的沉默通道。临床浓度的通用麻醉剂氟烷可特异性抑制C6大鼠胶质瘤细胞沉默钠通道的离子通量。在所测试的浓度下,N18细胞的电压依赖性通道对氟烷不敏感。