Presynaptic AMPA and kainate receptors increase the size of GABAergic terminals and enhance GABA release

Mónica L. Fiszman, Ferenc Erdélyi, Gábor Szabó, Stefano Vicini

Research output: Contribution to journalArticle

4 Citations (Scopus)


In the developing cerebellum, NMDA receptors promote the maturation of axonal terminals of inhibitory interneurons. We compared the effects of AMPA/kainate receptor agonists in cultured cerebellar cells from GAD65-eGFP mice. Both AMPA and kainate augmented granule cell survival without affecting interneurons. The action of kainate was blocked by an AMPA but not by a NMDA receptor antagonist, suggesting AMPA receptor involvement. AMPA and kainate increased the size of the GABAergic terminals and the action of kainate was insensitive to NMDA blockers. Whole cell recordings in granule neurons revealed that chronic treatment for 5 days with kainate as well as NMDA decreased AMPA receptor expression while interneuronal kainate receptors were depressed by kainate treatment. Acute kainate application increased mIPSCs frequency in both granule neurons and interneurons and this effect was only partially blocked by an AMPA receptor antagonist. In contrast to what was reported for NMDA, chronic treatment with kainate induced a significant decrease of the basal mIPSCs frequency but increased the acute action of kainate on mIPSCs. Direct recordings from presynaptic GABAergic terminals suggest that AMPA and kainate receptors are present in developing GABAergic terminals and their activation affects the size of GABAergic terminals and spontaneous GABA release.

Original languageEnglish
Pages (from-to)1631-1640
Number of pages10
Issue number8
Publication statusPublished - Jun 1 2007


  • Cerebellum
  • Interneuron
  • Patch-clamp
  • Survival
  • Synapses
  • eGFP

ASJC Scopus subject areas

  • Pharmacology
  • Cellular and Molecular Neuroscience

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