Sernagor E, Kuhn D, Vyklicky L, Mayer M L
Unit of Neurophysiology and Biophysics, NICHD, National Institutes of Health, Bethesda, Maryland 20892.
Neuron. 1989 Mar;2(3):1221-7. doi: 10.1016/0896-6273(89)90306-1.
The action of desipramine (DMI) and promazine on the response of mouse hippocampal neurons to the excitatory amino acid N-methyl-D-aspartic acid (NMDA) was investigated using whole-cell and single-channel recording. DMI at 20-50 microM was a potent, selective antagonist of responses to NMDA but not kainate or quisqualate. At -60 mV, the Kd for DMI block of responses to NMDA was 10 microM. The potency of DMI as an NMDA antagonist was highly voltage-dependent and behaved as though the Kd increased e-fold per 36 mV depolarization, reflecting an increase in the dissociation rate constant. Prior block of NMDA receptors with Mg2+ prevented binding of DMI, suggesting an action in the open channel. Single-channel analysis showed a decrease in the open time and burst length distributions, consistent with binding of DMI to open channels. We suggest that the action of DMI on NMDA receptor channels is similar to that of MK-801 and does not reflect binding to other domains, such as the regulatory sites for Zn2+ and glycine.
采用全细胞和单通道记录技术,研究了去甲丙咪嗪(DMI)和丙嗪对小鼠海马神经元对兴奋性氨基酸N-甲基-D-天冬氨酸(NMDA)反应的作用。20 - 50微摩尔的DMI是对NMDA反应的强效、选择性拮抗剂,但对 kainate 或 quisqualate 无此作用。在 -60 mV 时,DMI 阻断对 NMDA 反应的 Kd 为 10 微摩尔。DMI 作为 NMDA 拮抗剂的效力高度依赖电压,其表现似乎 Kd 每 36 mV 去极化增加 e 倍,反映了解离速率常数的增加。用 Mg2+ 预先阻断 NMDA 受体可防止 DMI 结合,提示其作用于开放通道。单通道分析显示开放时间和爆发长度分布减少,与 DMI 与开放通道的结合一致。我们认为 DMI 对 NMDA 受体通道的作用类似于 MK - 801,且不反映与其他结构域的结合,如 Zn2+ 和甘氨酸的调节位点。