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Ionotropic glutamate receptor modulation preferentially affects NMDA receptor expression in rat hippocampus

dc.contributor.authorHealy, Daniel J.en_US
dc.contributor.authorMeador-Woodruff, James H.en_US
dc.date.accessioned2006-04-19T14:02:48Z
dc.date.available2006-04-19T14:02:48Z
dc.date.issued2000-12-01en_US
dc.identifier.citationHealy, Daniel J.; Meador-Woodruff, James H. (2000)."Ionotropic glutamate receptor modulation preferentially affects NMDA receptor expression in rat hippocampus." Synapse 38(3): 294-304. <http://hdl.handle.net/2027.42/34990>en_US
dc.identifier.issn0887-4476en_US
dc.identifier.issn1098-2396en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34990
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11020232&dopt=citationen_US
dc.description.abstractElectrophysiological data suggest that alterations in the function of one glutamate receptor subtype may affect the function of other subtypes. Further, previous studies have demonstrated that NMDA receptor antagonists affect NMDA and kainate receptor expression in rat hippocampus. In order to address the mutual regulation of NMDA, AMPA, and kainate receptor expression in rat hippocampus, we conducted two experiments examining the effects of NMDA and non-NMDA glutamate receptor modulators on NMDA, AMPA, and kainate receptor expression using in situ hybridization and receptor autoradiography. NMDA receptor expression was preferentially affected by systemic treatments, as all drugs significantly altered [ 3 H]MK-801 binding, and several drugs increased [ 3 H]ifenprodil binding. GYKI52466 and aniracetam treatments resulted in changes in both [ 3 H]ifenprodil binding and NR2B mRNA levels, consistent with the association of this subunit and binding site in vitro. There were more modest effects on AMPA and kainate receptor expression, even by direct antagonists. Together, these data suggest that ionotropic glutamate receptors interact at the level of expression. These data also suggest that drug regimens targeting one ionotropic glutamate receptor subtype may indirectly affect other subtypes, potentially producing unwanted side effects. Synapse 38:294–304, 2000. © 2000 Wiley-Liss, Inc.en_US
dc.format.extent310941 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherNeuroscience, Neurology and Psychiatryen_US
dc.titleIonotropic glutamate receptor modulation preferentially affects NMDA receptor expression in rat hippocampusen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute and Department of Psychiatry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumMental Health Research Institute and Department of Psychiatry, University of Michigan, Ann Arbor, Michigan ; Mental Health Research Institute, Department of Psychiatry, University of Michigan, 205 Zina Pitcher Place, Ann Arbor, MI 48109-0720en_US
dc.identifier.pmid11020232en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34990/1/8_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1098-2396(20001201)38:3<294::AID-SYN8>3.0.CO;2-Uen_US
dc.identifier.sourceSynapseen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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