Tikhonova T B, Magazanik L G, Tikhonov D B
Ross Fiziol Zh Im I M Sechenova. 2010 Mar;96(3):237-46.
It is well known that ion composition significantly affects action of various pharmacological agents. In the present work we studied influence of external sodium on the block of Ca2+ -permeable AMPA receptor channels by dicationic derivative of phenylcyclohexyl IEM-1925. Experiments were performed on native receptors of giant striatal interneurones isolated from the rat brain slices. Registrations were done with the aid of whole-cell patch clamp technique. We found that partial substitution of external sodium by sucrose potentiated the blocking action of IEM-1925. The effect was voltage-dependent, being more pronounced at hyperpolarized voltages. The analysis of kinetics of the IEM-1925 action demonstrated that lowering of external sodium facilitated blocking action, whereas stability of the drug-channel complex remained unaffected. We conclude that the current carrying sodium ions compete with blocking cation IEM-1925 for an intrapore binding site.
众所周知,离子组成会显著影响各种药理剂的作用。在本研究中,我们研究了细胞外钠离子对苯基环己基双阳离子衍生物IEM - 1925阻断Ca2+通透型AMPA受体通道的影响。实验是在从大鼠脑片分离出的巨大纹状体中间神经元的天然受体上进行的。记录借助全细胞膜片钳技术完成。我们发现用蔗糖部分替代细胞外钠离子可增强IEM - 1925的阻断作用。该效应呈电压依赖性,在超极化电压下更为明显。对IEM - 1925作用动力学的分析表明,降低细胞外钠离子浓度会促进阻断作用,而药物 - 通道复合物的稳定性不受影响。我们得出结论,携带钠离子的电流与阻断阳离子IEM - 1925竞争孔内结合位点。