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pubmed-article:7901328pubmed:abstractTextRecent reports have suggested that a major proportion of [3H]kainate binding in goldfish brain is to a novel form of G-protein-linked glutamate receptor. Here we confirm that guanine nucleotides decrease [3H]kainate binding in goldfish brain membranes, but that binding is also reduced to a similar extent under conditions where G-protein modulation should be minimised. Inclusion of GTP gamma S resulted in an approximately twofold decrease in the affinity of [3H]kainate binding and a 50% reduction in the apparent Bmax values in both Mg2+/Na+ and Mg2+/Na(+)-free buffer when assayed at 0 degrees C. The pharmacology of [3H]kainate binding is similar to that of well-characterised ionotropic kainate receptors but unlike that of known metabotropic glutamate receptors, with neither 1S,3R-amino-1,3-cyclopentanedicarboxylic acid (1S,3R-ACPD) nor ibotenic acid being effective competitors. The molecular mass of the [3H]kainate binding protein, as determined by radiation inactivation, was 40 kDa, similar to the subunit sizes of other lower vertebrate kainate binding proteins that are believed to comprise ligand-gated ion channels. Furthermore, GTP gamma S also inhibited the binding of the non-NMDA receptor-selective antagonist 6-[3H]cyano-7-nitroquinoxaline-2,3-dione. These data strongly suggest that the regulatory interaction between guanine nucleotides and [3H]kainate and 6-[3H]cyano-7-nitroquinoxaline-2,3-dione binding is complex and involves competition at the agonist/antagonist binding site in addition to any G-protein-mediated modulation.lld:pubmed
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pubmed-article:7901328pubmed:authorpubmed-author:MurphyP APAlld:pubmed
pubmed-article:7901328pubmed:authorpubmed-author:BarnesJ MJMlld:pubmed
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pubmed-article:7901328pubmed:pagination1685-91lld:pubmed
pubmed-article:7901328pubmed:dateRevised2009-9-29lld:pubmed
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pubmed-article:7901328pubmed:articleTitleInteraction of guanine nucleotides with [3H]kainate and 6-[3H]cyano-7-nitroquinoxaline-2,3-dione binding in goldfish brain.lld:pubmed
pubmed-article:7901328pubmed:affiliationDepartment of Pharmacology, Medical School, University of Birmingham, England.lld:pubmed
pubmed-article:7901328pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7901328pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed