Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21011
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dc.contributor.authorJennes, Lothar-
dc.date.accessioned2021-07-02T13:34:34Z-
dc.date.available2021-07-02T13:34:34Z-
dc.date.issued1998-12-14-
dc.identifier.citationEyigör, Ö. ve Jennes, L. (1998). "Identification of kainate-preferring glutamate receptor subunit G1uR7 mRNA and protein in the rat median eminence". Brain Research, 814(1-2), 231-235.tr_TR
dc.identifier.issn0006-8993-
dc.identifier.urihttps://doi.org/10.1016/S0006-8993(98)01056-7-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0006899398010567-
dc.identifier.urihttp://hdl.handle.net/11452/21011-
dc.description.abstractIn situ hybridization and immunohistochemistry were used to determine the presence of kainate-preferring glutamate receptor subunits GluR6 and GluR7 mRNA and protein in the median eminence of the rat. The results show that most tanycytes lining the ventral third ventricle and many astrocytes within the median eminence contain the GluR7 receptor subunit mRNA but not the GluR5 and GluR6 receptor subunit mRNA. Immunohistochemical stainings show that the GluR6/7 receptor protein was localized to tanycytic cell bodies, their basal processes and to many other astrocytes in different layers of the median eminence. The results suggest that glutamate can act directly on the glial cells in the median eminence by binding to the GluR7 subunit which may be important for the control of the secretion of releasing and inhibiting hormones from axon terminals in the external layer. In order to determine if these receptor subunits are functional, kainic acid was injected and c-fos expression monitored. Results show that kainic acid induced c-Sos synthesis in most of these glial cells.tr_TR
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA NIH National Institute on Aging (NIA) - AG 13444tr_TR
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) - HD24697tr_TR
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA NIH Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD) - R01HD024697tr_TR
dc.description.sponsorshipUnited States Department of Health & Human Services National Institutes of Health (NIH) - USA NIH National Institute on Aging (NIA) - R01AG013444tr_TR
dc.language.isoentr_TR
dc.publisherElseviertr_TR
dc.rightsinfo:eu-repo/semantics/closedAccesstr_TR
dc.subjectNeurosciences & neurologytr_TR
dc.subjectKainic acidtr_TR
dc.subjectTanycytetr_TR
dc.subjectAstrocytetr_TR
dc.subjectIn situ hybridizationtr_TR
dc.subjectImmunocytochemistrytr_TR
dc.subjectC-fostr_TR
dc.subjectHormone-releasing hormonetr_TR
dc.subjectGrowth-factor-alphatr_TR
dc.subjectNeuroendocrine regulationtr_TR
dc.subjectExcitatory transmittertr_TR
dc.subjectCerebrospinal-fluidtr_TR
dc.subjectGlial-cellstr_TR
dc.subjectTanycytestr_TR
dc.subjectSecretiontr_TR
dc.subjectTerminalstr_TR
dc.subjectCloningtr_TR
dc.titleIdentification of kainate-preferring glutamate receptor subunit G1uR7 mRNA and protein in the rat median eminencetr_TR
dc.typeArticletr_TR
dc.identifier.wos000077849300028tr_TR
dc.identifier.scopus2-s2.0-0032517802tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-3463-7483tr_TR
dc.identifier.startpage231tr_TR
dc.identifier.endpage235tr_TR
dc.identifier.volume814tr_TR
dc.identifier.issue1-2tr_TR
dc.relation.journalBrain Researchtr_TR
dc.contributor.buuauthorEyigör, Özhan-
dc.contributor.researcheridABE-5128-2020tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed9838135tr_TR
dc.subject.wosNeurosciencestr_TR
dc.indexed.wosSCIEtr_TR
dc.indexed.scopusScopustr_TR
dc.indexed.pubmedPubmedtr_TR
dc.wos.quartileQ2tr_TR
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