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Kainate Receptor–Mediated Inhibition of Glutamate Release Involves Protein Kinase A in the Mouse Hippocampus
Author(s) -
José Vicente NegreteDíaz,
Talvinder S. Sihra,
José M. DelgadoGarcía,
Antonio Rodríguez Moreno
Publication year - 2006
Publication title -
journal of neurophysiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.302
H-Index - 245
eISSN - 1522-1598
pISSN - 0022-3077
DOI - 10.1152/jn.00280.2006
Subject(s) - kainate receptor , neuroscience , chemistry , glutamate receptor , metabotropic glutamate receptor , excitatory postsynaptic potential , postsynaptic potential , adenylyl cyclase , metabotropic receptor , forskolin , protein kinase a , ionotropic effect , stimulation , microbiology and biotechnology , receptor , biology , ampa receptor , inhibitory postsynaptic potential , biochemistry , kinase
The mechanisms involved in the inhibition of glutamate release mediated by the activation of presynaptic kainate receptors (KARs) at the hippocampal mossy fiber-CA3 synapse are not well understood. We have observed a long-lasting inhibition of CA3 evoked excitatory postsynaptic currents (eEPSCs) after a brief application of kainate (KA) at concentrations ranging from 0.3 to 10 muM. The inhibition outlasted the change in holding current caused by the activation of ionotropic KARs in CA3 pyramidal cells, indicating that this action is not contingent on the opening of the receptor channels. The inhibition of the eEPSCs by KA was prevented by G protein and protein kinase A (PKA) inhibitors and was enhanced after stimulation of the adenylyl cyclase (AC) with forskolin. We conclude that KARs present at mossy fiber terminals mediate the inhibition of glutamate release through a metabotropic mechanism that involves the activation of an AC-second messenger cAMP-PKA signaling cascade.

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