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PMID: 9517417 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The synaptic activation of the GluR5 subtype of kainate receptor in area CA3 of the rat hippocampus.

Neuropharmacology ·Vol. 36 ·No. 11-12 ·1997-00-00 ·Pages 1477-81

Vignes M, Bleakman D, Lodge D, Collingridge GL

Abstract

Two new compounds (LY293558 and LY294486), that antagonize homomeric human GluR5 receptors, were examined against responses mediated by kainate receptors in the CA3 region of rat hippocampal slices. Both compounds (applied at a concentration of 10 microM) antagonized reversibly currents induced by 200 nM kainate. They also antagonized reversibly the synaptic activation of kainate receptors, evoked by high-frequency stimulation of mossy fibres, in the presence of NMDA and AMPA receptor antagonists. These results show that GluR5 subunits are likely to contribute to a kainate receptor on CA3 neurones that mediates responses to both kainate and synaptically-released L-glutamate.

MeSH Terms
Animals Excitatory Amino Acid Antagonists/pharmacology Hippocampus/metabolism,physiology In Vitro Techniques Isoquinolines/pharmacology Male Rats Rats, Wistar Receptors, AMPA/antagonists & inhibitors Receptors, Glutamate/metabolism,physiology Receptors, Kainic Acid/antagonists & inhibitors,metabolism,physiology Synapses/physiology Tetrazoles/pharmacology
Chemicals
Excitatory Amino Acid Antagonists Isoquinolines LY 294486 Receptors, AMPA Receptors, Glutamate Receptors, Kainic Acid Tetrazoles tezampanel
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Vignes M
Department of Anatomy, University of Bristol, UK.
Bleakman D
Lodge D
Collingridge G L
Article Info
Journal
Neuropharmacology
Abbr.
Neuropharmacology
ISSN
0028-3908
Published
1997-00-00
Pages
1477-81
Language
English
Region
England
NLM ID
0236217
Subset
IM
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