Duguid Ian C, Smart Trevor G
Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.
Nat Neurosci. 2004 May;7(5):525-33. doi: 10.1038/nn1227. Epub 2004 Apr 18.
Synaptic inhibition is a vital component in the control of cell excitability within the brain. Here we report a newly identified form of inhibitory synaptic plasticity, termed depolarization-induced potentiation of inhibition, in rodents. This mechanism strongly potentiated synaptic transmission from interneurons to Purkinje cells after the termination of depolarization-induced suppression of inhibition. It was triggered by an elevation of Ca(2+) in Purkinje cells and the subsequent retrograde activation of presynaptic NMDA receptors. These glutamate receptors promoted the spontaneous release of Ca(2+) from presynaptic ryanodine-sensitive Ca(2+) stores. Thus, NMDA receptor-mediated facilitation of transmission at this synapse provides a regulatory mechanism that can dynamically alter the synaptic efficacy at inhibitory synapses.
突触抑制是大脑中控制细胞兴奋性的重要组成部分。在此,我们报告了在啮齿动物中一种新发现的抑制性突触可塑性形式,称为去极化诱导的抑制增强。在去极化诱导的抑制抑制终止后,这种机制强烈增强了中间神经元到浦肯野细胞的突触传递。它由浦肯野细胞中Ca(2+)升高及随后突触前NMDA受体的逆行激活触发。这些谷氨酸受体促进了Ca(2+)从突触前对ryanodine敏感的Ca(2+)储存库的自发释放。因此,NMDA受体介导的该突触传递促进作用提供了一种调节机制,可动态改变抑制性突触的突触效能。