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Expression patterns of corticotropin-releasing factor, arginine vasopressin, histidine decarboxylase, melanin-concentrating hormone, and orexin genes in the human hypothalamus

dc.contributor.authorKrolewski, David M.en_US
dc.contributor.authorMedina, Adrianaen_US
dc.contributor.authorKerman, Ilan A.en_US
dc.contributor.authorBernard, Reneen_US
dc.contributor.authorBurke, Sharonen_US
dc.contributor.authorThompson, Robert C.en_US
dc.contributor.authorBunney, William E.en_US
dc.contributor.authorSchatzberg, Alan F.en_US
dc.contributor.authorMyers, Richard M.en_US
dc.contributor.authorAkil, Hudaen_US
dc.contributor.authorJones, Edward G.en_US
dc.contributor.authorWatson, Stanley J.en_US
dc.date.accessioned2010-10-06T14:57:20Z
dc.date.available2011-03-01T16:26:44Zen_US
dc.date.issued2010-11-15en_US
dc.identifier.citationKrolewski, David M.; Medina, Adriana; Kerman, Ilan A.; Bernard, Rene; Burke, Sharon; Thompson, Robert C.; Bunney, William E.; Schatzberg, Alan F.; Myers, Richard M.; Akil, Huda; Jones, Edward G.; Watson, Stanley J. (2010). "Expression patterns of corticotropin-releasing factor, arginine vasopressin, histidine decarboxylase, melanin-concentrating hormone, and orexin genes in the human hypothalamus." The Journal of Comparative Neurology 518(22): 4591-4611. <http://hdl.handle.net/2027.42/78077>en_US
dc.identifier.issn0021-9967en_US
dc.identifier.issn1096-9861en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78077
dc.description.abstractThe hypothalamus regulates numerous autonomic responses and behaviors. The neuroactive substances corticotropin-releasing factor (CRF), arginine-vasopressin (AVP), histidine decarboxylase (HDC), melanin-concentrating hormone (MCH), and orexin/hypocretins (ORX) produced in the hypothalamus mediate a subset of these processes. Although the expression patterns of these genes have been well studied in rodents, less is known about them in humans. We combined classical histological techniques with in situ hybridization histochemistry to produce both 2D and 3D images and to visually align and quantify expression of the genes for these substances in nuclei of the human hypothalamus. The hypothalamus was arbitrarily divided into rostral, intermediate, and caudal regions. The rostral region, containing the paraventricular nucleus (PVN), was defined by discrete localization of CRF- and AVP-expressing neurons, whereas distinct relationships between HDC, MCH, and ORX mRNA-expressing neurons delineated specific levels within the intermediate and caudal regions. Quantitative mRNA signal intensity measurements revealed no significant differences in overall CRF or AVP expression at any rostrocaudal level of the PVN. HDC mRNA expression was highest at the level of the premammillary area, which included the dorsomedial and tuberomammillary nuclei as well as the dorsolateral hypothalamic area. In addition, the overall intensity of hybridization signal exhibited by both MCH and ORX mRNA-expressing neurons peaked in distinct intermediate and caudal hypothalamic regions. These results suggest that human hypothalamic neurons involved in the regulation of the HPA axis display distinct neurochemical patterns that may encompass multiple local nuclei. J. Comp. Neurol. 518:4591–4611, 2010. © 2010 Wiley-Liss, Inc.en_US
dc.format.extent1685527 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherNeuroscience, Neurology and Psychiatryen_US
dc.titleExpression patterns of corticotropin-releasing factor, arginine vasopressin, histidine decarboxylase, melanin-concentrating hormone, and orexin genes in the human hypothalamusen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNeurosciencesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109 ; Department of Psychiatry, University of California, Irvine, California 92697en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumMolecular & Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationotherDepartment of Psychiatry, University of California, Irvine, California 92697en_US
dc.contributor.affiliationotherPsychiatry Department, Stanford University School of Medicine, Stanford, California 94305en_US
dc.contributor.affiliationotherHudsonAlpha Institute for Biotechnology, Huntsville, Alabama 35806en_US
dc.contributor.affiliationotherCenter for Neuroscience, University of California, Davis, California 956108 ; Center for Neuroscience, 1544 Newton Court, Davis, CA 95618en_US
dc.identifier.pmid20886624en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78077/1/22480_ftp.pdf
dc.identifier.doi10.1002/cne.22480en_US
dc.identifier.sourceThe Journal of Comparative Neurologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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