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Diurnal Regulation of Glucocorticoid Receptor and Mineralocorticoid Receptor mRNAs in Rat Hippocampus

dc.contributor.authorHerman, James P.en_US
dc.contributor.authorWatson, Stanley J.en_US
dc.contributor.authorChao, Helen M.en_US
dc.contributor.authorCoirini, Hectoren_US
dc.contributor.authorMcEwen, Bruce S.en_US
dc.date.accessioned2006-04-10T15:48:41Z
dc.date.available2006-04-10T15:48:41Z
dc.date.issued1993-04en_US
dc.identifier.citationHerman, James P., Watson, Stanley J., Chao, Helen M., Coirini, Hector, McEwen, Bruce S. (1993/04)."Diurnal Regulation of Glucocorticoid Receptor and Mineralocorticoid Receptor mRNAs in Rat Hippocampus." Molecular and Cellular Neuroscience 4(2): 181-190. <http://hdl.handle.net/2027.42/30866>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WNB-45P68BT-1X/2/f02e7ebe2c20b203d860dfd3f44b11bfen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30866
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19912921&dopt=citationen_US
dc.description.abstractThe present studies were undertaken to determine whether hippocampal glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) biosynthesis, as inferred from mRNA expression, exhibit diurnal patterns of activation which may reflect or predict changes in plasma adrenocorticosteroid levels. Animals received either adrenalectomy (ADX) or sham adrenalectomy and were sacrificed at 4-h intervals throughout the diurnal cycle. Hippocampal and control brain areas were assayed for regional GR and MR mRNA changes via semiquantitative in situ hybridization histochemical analysis. The results indicate subfield-specific significant circadian rhythms in both GR and MR mRNAs. A significant diurnal rhythm in GR mRNA expression was seen in the dentate gyrus (DG), which took the shape of a monotonic curve with a marked trough at 1500 h after lights on (1 h after lights off). A similar pattern was evident in subfield CA1, although the effect fell short of statistical significance. No rhythm was seen in CA3. In response to ADX, GR mRNA was markedly increased in both CA1 and CA3; these increases appeared to be independent of circadian influences. In contrast, ADX effects in DG were quite limited and appeared to eliminate the circadian GR mRNA trough. Bimodal diurnal rhythms in MR mRNA expression were observed in all subfields and commonly exhibited troughs at 1500 h after lights on and 0300 h after lights on. These rhythms appeared to be related to circulating steroids, as ADX eliminated both the 1500 and 0300 h troughs, resulting in flat levels of MR mRNA expression corresponding roughly to the circadian peak. Notably, no diurnal GR or MR mRNA rhythms were observed in frontoparietal cortex, nor were any GR mRNA changes seen in the dorsomedial thalamus or hypothalamic paraventricular nucleus. Indeed, ADX was ineffective in altering adrenocorticosteroid receptor mRNA expression in any extrahippocampal region examined. These results indicate that GR and MR mRNAs exhibit hippocampus-specific diurnal rhythms in expression which are controlled to a greater (MR) or lesser (GR) extent by circulating steroids. The apparent steroid sensitivity of hippocampal adrenocorticosteroid receptor populations may be involved in the expression of rhythmic changes in hippocampal function associated with HPA regulation and information processing.en_US
dc.format.extent758510 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleDiurnal Regulation of Glucocorticoid Receptor and Mineralocorticoid Receptor mRNAs in Rat Hippocampusen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPsychologyen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, 205 Zina Pitcher Place, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationotherDepartment of Anatomy and Neurobiology, University of Kentucky Medical Center, 800 Rose Street, Lexington, Kentucky, USA.en_US
dc.contributor.affiliationotherLaboratory of Neuroendocrinology, Rockefeller University, 1230 York Avenue, New York, New York, USA.en_US
dc.contributor.affiliationotherLaboratory of Neuroendocrinology, Rockefeller University, 1230 York Avenue, New York, New York, USA.en_US
dc.contributor.affiliationotherLaboratory of Neuroendocrinology, Rockefeller University, 1230 York Avenue, New York, New York, USA.en_US
dc.identifier.pmid19912921en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30866/1/0000529.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/mcne.1993.1022en_US
dc.identifier.sourceMolecular and Cellular Neuroscienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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