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Chronic electroconvulsive shock treatment elicits up-regulation of CRF and AVP mRNA in select populations of neuroendocrine neurons

dc.contributor.authorHerman, James P.en_US
dc.contributor.authorSchafer, Martin K.-H.en_US
dc.contributor.authorSladek, Celia D.en_US
dc.contributor.authorDay, Roberten_US
dc.contributor.authorYoung, Elizabeth A.en_US
dc.contributor.authorAkil, Hudaen_US
dc.contributor.authorWatson, Stanley J.en_US
dc.date.accessioned2006-04-07T20:39:10Z
dc.date.available2006-04-07T20:39:10Z
dc.date.issued1989-11-06en_US
dc.identifier.citationHerman, James P., Schafer, Martin K. -H., Sladek, Celia D., Day, Robert, Young, Elizabeth A., Akil, Huda, Watson, Stanley J. (1989/11/06)."Chronic electroconvulsive shock treatment elicits up-regulation of CRF and AVP mRNA in select populations of neuroendocrine neurons." Brain Research 501(2): 235-246. <http://hdl.handle.net/2027.42/27688>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6SYR-4840J6F-5P/2/b814e95c70173d46a0f984fc3dc82130en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27688
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2819439&dopt=citationen_US
dc.description.abstractThe effects of repeated electroconvulsive seizures (ECS) on expression of mRNAs coding for corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) in neuroendocrine neurons of the hypothalamo-pituitary-adrenocortical (HPA) axis and hypothalamo-neurohypophysial system (HNS) were assessed via semi-quantitative in situ hybridization histochemical analysis. Measures of mRNA content were accompanied by measurement of peptide- and hormone-expression in the relevant neuroendocrine systems. Following 7 daily ECS treatments, CRF mRNA was significantly increased in the medial parvocellular paraventricular nucleus (PVN) of treated rats relative to controls. CRF peptide content of whole PVN homogenates was decreased to 50% of control levels. Changes in CRF message and peptide levels were accompanied by increases in pituitary ACTH content and by elevated plasma corticosterone, suggesting ECS elicits long-term up-regulation of the HPA axis. AVP mRNA in the medial parvocellular PVN, which is known to up-regulate in response to HPA challenge by adrenalectomy, was not increased by ECS. Chronic ECS causes a clear up-regulation of HNS neurons of the supraoptic nucleus, characterized by increased AVP mRNA content, decreased AVP peptide content, and depletion of neurohypophysial AVP. However, no changes were observed in magnocellular vasopressinergic neurons of the PVN, indicating that magnocellular SON and PVN neurons respond differentially to stimulation by ECS. The data indicate that ECS is a potent stimulus for activation of select components of both the HPA axis and the HNS. As such, ECS provides a useful tool for examining mechanism underlying neuroendocrine processes.en_US
dc.format.extent1028626 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleChronic electroconvulsive shock treatment elicits up-regulation of CRF and AVP mRNA in select populations of neuroendocrine neuronsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationumMental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.en_US
dc.contributor.affiliationotherDepartment of Neurobiology and Anatomy, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, U.S.A.en_US
dc.identifier.pmid2819439en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27688/1/0000072.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0006-8993(89)90641-0en_US
dc.identifier.sourceBrain Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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