Bayazitov I T, Voronin L L, Kas'yanov A M, Kleshchevnikov A M, Kul'hitskii S V, Sametskii E A
Institute of the Brain, Russian Academy of Medical Sciences, Moscow.
Neurosci Behav Physiol. 2002 Sep-Oct;32(5):533-40. doi: 10.1023/a:1019867808419.
The aim of the present work was to study the potentiation of the AMPA and NMDA components of minimal excitatory postsynaptic currents (EPSC) evoked by activation of restricted numbers of synapses. EPSC of neurons in field CA1 in hippocampal slices were recorded in whole-call patch-clamp conditions selected such that both (AMPA and NMDA) components were present, and these were measured in parallel using computational methods in combination with pharmacological receptor blockade. There was a quite strong correlation between the amplitudes of the AMPA and NMDA components and this was regarded as evidence that they were generated by the same synapses. In cases producing this correlation, both components showed essentially equal long-term potentiation lasting from 5 min to 2 h after afferent tetanization. The data did not support the postsynaptic hypothesis and were in better agreement with the concept that the major mechanism for the persistence of the initial phase of long-term potentiation (up to 1-2 h) is based on increases in the quantity of transmitter released presynaptically.
本研究的目的是研究通过激活有限数量的突触所诱发的最小兴奋性突触后电流(EPSC)中AMPA和NMDA成分的增强作用。在全细胞贴片钳条件下记录海马切片中CA1区神经元的EPSC,选择该条件是为了使两种成分(AMPA和NMDA)均存在,并使用计算方法结合药理学受体阻断对其进行平行测量。AMPA和NMDA成分的幅度之间存在相当强的相关性,这被视为它们由相同突触产生的证据。在产生这种相关性的情况下,两种成分在传入强直刺激后5分钟至2小时内均表现出基本相等的长时程增强。数据不支持突触后假说,且与长期增强初始阶段(长达1-2小时)持续存在的主要机制基于突触前释放递质数量增加这一概念更为一致。