Mike A, Dyatlov V A, Vizi E S
Department of Pharmacology, Hungarian Academy of Sciences, Budapest, Hungary.
Neuroreport. 1996 Nov 4;7(15-17):2613-7. doi: 10.1097/00001756-199611040-00041.
The effect of kainate on the voltage-activated current of cultured embryonic chick telencephalic neurones was studied by whole-cell voltage clamp recording. In addition to opening non-NMDA receptor coupled ion channels, kainate produced additional effects, with a slower time course: it modulated voltage-activated currents. These effects were blocked by the non-NMDA receptor antagonists CNQX (6-cyano-7-nitroquinoxaline-2,3-dione) and GYKI 53784 ((-)-1-(4-aminophenyl)-3- methylcarbamoyl-4-methyl-7,8-methylenedioxy-3,4- dihydro-5H-2,3-benzodiazepine), indicating that non NMDA receptors are involved. It has been shown that the reversible inhibition of outward potassium currents was partly due to a decrease of current amplitude and partly to a marked shift of the inactivation curve towards more negative potentials.
通过全细胞膜片钳记录研究了红藻氨酸对培养的胚胎鸡端脑神经元电压激活电流的影响。除了打开与非NMDA受体偶联的离子通道外,红藻氨酸还产生了其他作用,其时间进程较慢:它调节电压激活电流。这些作用被非NMDA受体拮抗剂CNQX(6-氰基-7-硝基喹喔啉-2,3-二酮)和GYKI 53784((-)-1-(4-氨基苯基)-3-甲基氨基甲酰基-4-甲基-7,8-亚甲基二氧基-3,4-二氢-5H-2,3-苯并二氮杂卓)阻断,表明涉及非NMDA受体。已经表明,外向钾电流的可逆抑制部分是由于电流幅度的降低,部分是由于失活曲线明显向更负的电位移动。