Barker J L, McBurney R N, Mathers D A
Br J Pharmacol. 1983 Dec;80(4):619-29. doi: 10.1111/j.1476-5381.1983.tb10051.x.
A two-microelectrode voltage-clamp technique was used to record membrane current responses induced by the application of the neutral amino acids, gamma-aminobutyric acid (GABA) and glycine, to mouse spinal neurones maintained in cell culture. Membrane current responses to GABA were depressed by the convulsant agents, bicuculline, picrotoxin and pentylenetetrazole. Membrane current responses to glycine were depressed by the convulsant compound, strychnine. Analysis of the fluctuations in membrane current about the mean response during prolonged applications of GABA revealed that neither the conductance nor the average open-time of GABA-activated ion-channels was altered in the presence of picrotoxin or bicuculline. Pentylenetetrazole caused a reduction in the open-time of GABA-activated ion-channels but this effect alone was too small to account for the depression of the current response. A similar analysis of glycine-induced responses in the presence of strychnine revealed that the depression of glycine responses by strychnine was not associated with any changes in the conductance or average open-time of glycine-activated ion-channels. We therefore conclude that the convulsant compounds act by reducing the rate of activation of ion-channels by the neutral amino acids either through a reduction in the number of free receptors or by a change in the kinetics of channel activation.
采用双微电极电压钳技术,记录在细胞培养中维持的小鼠脊髓神经元上,施加中性氨基酸、γ-氨基丁酸(GABA)和甘氨酸所诱导的膜电流反应。惊厥剂荷包牡丹碱、苦味毒和戊四氮可抑制对GABA的膜电流反应。惊厥化合物士的宁可抑制对甘氨酸的膜电流反应。对长时间施加GABA期间膜电流围绕平均反应的波动分析表明,在存在苦味毒或荷包牡丹碱的情况下,GABA激活的离子通道的电导和平均开放时间均未改变。戊四氮导致GABA激活的离子通道开放时间缩短,但仅此效应太小,无法解释电流反应的抑制。在存在士的宁的情况下对甘氨酸诱导反应的类似分析表明,士的宁对甘氨酸反应的抑制与甘氨酸激活的离子通道的电导或平均开放时间的任何变化均无关。因此,我们得出结论,惊厥化合物的作用是通过减少中性氨基酸对离子通道的激活速率,这要么是通过减少游离受体的数量,要么是通过改变通道激活的动力学来实现的。