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Behaviour of NMDA and AMPA receptor-mediated miniature EPSCs at rat cortical neuron synapses identified by calcium imaging

机译:NMDA和AMPA受体介导的微型EPSC在通过钙成像确定的大鼠皮质神经元突触中的行为

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摘要

Simultaneous recording of intracellular calcium concentration at a synapse and synaptic currents from the cell body allows mapping of miniature excitatory postsynaptic currents (mEPSCs) to single synapses.In the absence of extracellular Mg2+, 77% of synapses had mEPSCs with fast and slow components, attributed to AMPA- and NMDA-type glutamate receptors, respectively. The remainder of synapses (23%) had mEPSCs that lacked a fast component; these responses were attributed to NMDA receptors.A strong positive correlation between the amplitude of the calcium transient and the NMDA receptor-mediated mEPSC was observed, indicating that the mEPSCs originate from an identified synapse.At synapses that had both mEPSC components, the AMPA receptor component was positively correlated with charge influx mediated by NMDA receptors during repeated synaptic events. No periodic failure in the AMPA receptor mEPSC was observed at synapses expressing both receptor components.A significant positive correlation between the mean amplitudes of NMDA and AMPA receptor components of mEPSCs is observed across different synapses.We suggest that factors effecting both receptor classes, such as the amount of transmitter in synaptic vesicles, might contribute to the variation in mEPSC amplitude during repeated miniature events at a single synapse. Although the average postsynaptic response at different synapses can vary in amplitude, there appears to be a mechanism to keep the ratio of each receptor subtype within a narrow range.
机译:同时记录突触中细胞内钙浓度和细胞体中的突触电流,可以将小型兴奋性突触后电流(mEPSC)映射到单个突触。在没有细胞外Mg2 +的情况下,有77%的突触具有快速和慢速成分的mEPSC。分别针对AMPA和NMDA型谷氨酸受体。其余的突触(23%)具有缺乏快速成分的mEPSC。这些反应归因于NMDA受体。观察到钙瞬变幅度与NMDA受体介导的mEPSC之间存在很强的正相关性,这表明mEPSCs来自已鉴定的突触。在同时具有mEPSC成分的突触中,AMPA受体在反复的突触事件中,该组分与NMDA受体介导的电荷流入呈正相关。在表达两种受体成分的突触中均未观察到AMPA受体mEPSC的周期性衰竭。在不同突触中观察到mEPSC的NMDA平均振幅与AMPA受体成分之间的显着正相关。突触小泡中递质的数量可能会导致在单个突触中重复的微型事件期间mEPSC振幅的变化。尽管在不同突触处的平均突触后反应的幅度可以变化,但似乎存在一种将每种受体亚型的比率保持在狭窄范围内的机制。

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