Marcaggi Païkan, Attwell David
Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.
J Physiol. 2007 Jan 15;578(Pt 2):545-50. doi: 10.1113/jphysiol.2006.115014. Epub 2006 Nov 16.
Cerebellar granule cell to Purkinje cell synapses have been reported to show plasticity when stimulating the parallel fibres, but not when granule cell axons are stimulated in the granular layer. The latter absence of plasticity has been attributed either to the synapses made by ascending granule cell axons lacking some feature needed to evoke plasticity, such as metabotropic glutamate receptors, or to spillover of glutamate between adjacent active synapses being essential for plasticity to occur and having a greater effect for parallel fibre stimulation than for granular layer stimulation. Here we show that both long-term depression (LTD) and endocannabinoid plasticity can depend on interaction between adjacent synapses. These results focus attention on the need to characterize the spatial pattern of parallel fibre activity evoked by physiological stimuli, in order to assess the conditions under which synaptic plasticity will occur in vivo.
据报道,当刺激平行纤维时,小脑颗粒细胞与浦肯野细胞之间的突触会表现出可塑性,但在颗粒层刺激颗粒细胞轴突时则不会。后者缺乏可塑性的原因,要么是上升的颗粒细胞轴突形成的突触缺乏引发可塑性所需的某些特征,如代谢型谷氨酸受体;要么是相邻活跃突触之间谷氨酸的溢出对可塑性的发生至关重要,且对平行纤维刺激的影响比对颗粒层刺激的影响更大。在这里,我们表明长期抑制(LTD)和内源性大麻素可塑性都可能取决于相邻突触之间的相互作用。这些结果将注意力集中在需要表征生理刺激诱发的平行纤维活动的空间模式上,以便评估体内突触可塑性发生的条件。