Konnerth A, Keller B U, Ballanyi K, Yaari Y
Zelluläre Neurophysiologie, Max-Planck-Institut für biophysikalische Chemie, Göttingen, Federal Republic of Germany.
Exp Brain Res. 1990;81(1):209-12. doi: 10.1007/BF00230117.
Patch-clamp techniques were used to record pharmacologically-isolated N-methyl-D-aspartate-mediated excitatory postsynaptic currents (NMDA-EPSCs) from dentate granule cells in thin rat hippocampal slices. Membrane voltage modulated these EPSCs in two ways. Firstly, depolarization from resting potential enhanced EPSC amplitudes, as expected for a voltage-dependent block by Mg2+ of synaptically activated NMDA receptor channels. Secondly, depolarization markedly prolonged the time course of decay of NMDA-EPSCs in normal and low extracellular Mg2+. Both mechanisms were complementary in establishing a strong dependence between membrane potential and the amount of charge, namely Ca2+, transferred through synaptically activated NMDA receptor channels, that presumably underlies induction of long-term potentiation in the hippocampus.
采用膜片钳技术记录来自薄的大鼠海马切片齿状颗粒细胞的药理学分离的N-甲基-D-天冬氨酸介导的兴奋性突触后电流(NMDA-EPSCs)。膜电压以两种方式调节这些EPSCs。首先,从静息电位去极化增强了EPSC幅度,这正如突触激活的NMDA受体通道被Mg2+电压依赖性阻断所预期的那样。其次,去极化显著延长了正常和低细胞外Mg2+条件下NMDA-EPSCs的衰减时间进程。这两种机制在建立膜电位与通过突触激活的NMDA受体通道转移的电荷量(即Ca2+)之间的强烈依赖性方面是互补的,这可能是海马体中长时程增强诱导的基础。