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突触前钙在海马苔藓纤维突触短期增强中的作用。

The role of presynaptic calcium in short-term enhancement at the hippocampal mossy fiber synapse.

作者信息

Regehr W G, Delaney K R, Tank D W

机构信息

AT&T Bell Laboratories, Murray Hill, New Jersey 07974.

出版信息

J Neurosci. 1994 Feb;14(2):523-37. doi: 10.1523/JNEUROSCI.14-02-00523.1994.

Abstract

The mossy fiber synapse between dentate granule cells and CA3 pyramidal cells in the guinea pig hippocampus shows a robust short-term synaptic enhancement. We have simultaneously measured presynaptic residual free calcium ([Ca2+]i) and postsynaptic field potentials at this synapse to examine the role of [Ca2+]i in this enhancement. Single action potentials produced an increase in [Ca2+]i of 10-50 nM that decayed to resting levels with a time constant of about 1 sec. Trains of action potentials produced larger [Ca2+]i increases that returned more slowly to resting levels. Following the onset of moderate frequency stimulus trains (0.1-5 Hz), synaptic transmission and [Ca2+]i both increased and eventually plateaued. During the steady-state phase a linear relationship between [Ca2+]i and synaptic enhancement was observed. During the initial buildup, however, [Ca2+]i rose more rapidly than synaptic enhancement. Similarly, during the decay phase immediately following termination of a stimulus train, [Ca2+]i returned to prestimulus levels faster than synaptic enhancement. High concentrations of the calcium buffer EGTA in the presynaptic terminal slowed the buildup and decay of both [Ca2+]i and synaptic enhancement produced by stimulus trains. Under these conditions, the time course of [Ca2+]i and synaptic enhancement were well matched. This suggests that, despite the differences in kinetic rates observed for normal buffering conditions, increases in [Ca2+]i play a causal role in short-term enhancement. An increase in [Ca2+]i of 10-30 nM produced a twofold enhancement. We propose a simple kinetic model to explain these results. The model assumes that synaptic enhancement is controlled by a Ca-dependent first-order reaction. According to this scheme, a change in [Ca2+]i alters neurotransmitter release, but the slow kinetics of the underlying reaction introduces a temporal filter, producing a delay in the change in synaptic enhancement.

摘要

豚鼠海马齿状颗粒细胞与CA3锥体细胞之间的苔藓纤维突触表现出强烈的短期突触增强。我们在此突触处同时测量了突触前残余游离钙([Ca2+]i)和突触后场电位,以研究[Ca2+]i在这种增强中的作用。单个动作电位使[Ca2+]i增加10 - 50 nM,其以约1秒的时间常数衰减至静息水平。一连串的动作电位使[Ca2+]i增加得更多,且恢复到静息水平的速度更慢。在中等频率刺激串(0.1 - 5 Hz)开始后,突触传递和[Ca2+]i均增加并最终趋于平稳。在稳态阶段,观察到[Ca2+]i与突触增强之间存在线性关系。然而,在初始增强阶段,[Ca2+]i上升比突触增强更快。同样,在刺激串终止后的衰减阶段,[Ca2+]i恢复到刺激前水平比突触增强更快。突触前终末中高浓度的钙缓冲剂EGTA减缓了刺激串产生的[Ca2+]i和突触增强的增强和衰减过程。在这些条件下,[Ca2+]i和突触增强的时间进程良好匹配。这表明,尽管在正常缓冲条件下观察到动力学速率存在差异,但[Ca2+]i的增加在短期增强中起着因果作用。[Ca2+]i增加10 - 30 nM会产生两倍的增强作用。我们提出一个简单的动力学模型来解释这些结果。该模型假设突触增强由钙依赖性一级反应控制。根据此方案,[Ca2+]i的变化会改变神经递质释放,但基础反应的缓慢动力学引入了一个时间滤波器,导致突触增强变化出现延迟。

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