Hessler N A, Shirke A M, Malinow R
Neuroscience Program, University of Iowa, Iowa City 52242.
Nature. 1993 Dec 9;366(6455):569-72. doi: 10.1038/366569a0.
When an action potential reaches a synaptic terminal, fusion of a transmitter-containing vesicle with the presynaptic membrane occurs with a probability (pr) of less than one. Despite the fundamental importance of this parameter, pr has not been directly measured in the central nervous system. Here we describe a novel approach to determine pr, monitoring the decrement of NMDA (N-methyl-D-aspartate)-receptor mediated synaptic currents in the presence of the use-dependent channel blocker MK-801 (ref. 2). On a single postsynaptic CA1 hippocampal slice neuron, two classes of synapses with a sixfold difference in pr are resolved. Synapses with low pr contribute to over half of transmission and are more sensitive to drugs enhancing transmitter release. Switching between these two classes of synapses provides the potential for large changes in synaptic efficacy and could underlie forms of activity-dependent plasticity.
当动作电位到达突触终末时,含递质的囊泡与突触前膜融合的概率(pr)小于1。尽管该参数具有根本重要性,但pr尚未在中枢神经系统中直接测量。在此,我们描述一种确定pr的新方法,即在使用依赖性通道阻滞剂MK-801存在的情况下监测N-甲基-D-天冬氨酸(NMDA)受体介导的突触电流的衰减(参考文献2)。在单个海马CA1区突触后切片神经元上,分辨出两类pr相差6倍的突触。pr低的突触对超过一半的传递有贡献,并且对增强递质释放的药物更敏感。在这两类突触之间切换为突触效能的大幅变化提供了可能性,并且可能是活动依赖性可塑性形式的基础。