Davies S N, Collingridge G L
Department of Pharmacology, University of Bristol, School of Medical Sciences, U.K.
Proc R Soc Lond B Biol Sci. 1989 May 22;236(1285):373-84. doi: 10.1098/rspb.1989.0028.
The new antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), which blocks responses to kainate and quisqualate, has been used in conjunction with D-2-amino-5-phosphonovalerate (APV), which blocks selectively responses to N-methyl-D-aspartate (NMDA), to determine the role of excitatory amino acid receptors in synaptic transmission. An excitatory postsynaptic potential (EPSP)-inhibitory postsynaptic potential (IPSP) sequence was evoked in CA1 neurons by stimulation of the Schaffer collateral-commissural pathway in rat hippocampal slices. CNQX (10 microM) substantially reduced the EPSP without having any effect on input resistance or membrane potential. The IPSP was also reduced provided that the stimulating electrode was place approximately 1 mm from the recording electrode. The EPSP that remained in the presence of CNQX had characteristics of an NMDA receptor-mediated potential; it had a slow timecourse, summated at high frequencies, was blocked reversibly by APV, increased greatly in size in Mg2+-free medium, and showed an anomalous voltage dependence in Mg2+-containing medium. In the presence of CNQX, an APV-sensitive polysynaptic GABAergic IPSP could be evoked, indicating that NMDA receptors can mediate suprathreshold EPSPS in inhibitory interneurons. It is suggested that either NMDA or non-NMDA receptors can, under different circumstances, mediate the synaptic excitation of pyramidal neurons and inhibitory interneurons in area CA1 of the hippocampus.
新型拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)可阻断对海人藻酸和quisqualate的反应,它已与D-2-氨基-5-磷酸戊酸(APV)联合使用,后者可选择性阻断对N-甲基-D-天冬氨酸(NMDA)的反应,以确定兴奋性氨基酸受体在突触传递中的作用。通过刺激大鼠海马切片中的Schaffer侧支-连合通路,在CA1神经元中诱发了兴奋性突触后电位(EPSP)-抑制性突触后电位(IPSP)序列。CNQX(10 microM)可显著降低EPSP,而对输入电阻或膜电位没有任何影响。如果刺激电极放置在距记录电极约1 mm处,IPSP也会降低。在CNQX存在的情况下残留的EPSP具有NMDA受体介导电位的特征;它具有缓慢的时间进程,在高频下总和,可被APV可逆性阻断,在无镁培养基中大小显著增加,并且在含镁培养基中表现出异常的电压依赖性。在CNQX存在的情况下,可诱发APV敏感的多突触GABA能IPSP,这表明NMDA受体可介导抑制性中间神经元中的阈上EPSP。提示在不同情况下,NMDA或非NMDA受体均可介导海马CA1区锥体细胞和抑制性中间神经元的突触兴奋。