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Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis
High densities of nerve cells containing corticotropin-releasing hormone (CRH) are located in the central nucleus of the amygdala (CeA) and paraventricular nucleus (PVN) of the hypothalamus. These brain regions play an important role in activating autonomic, behavioral, and endocrine responses to st...
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Published in: | Brain research 1998-03, Vol.788 (1), p.305-310 |
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description | High densities of nerve cells containing corticotropin-releasing hormone (CRH) are located in the central nucleus of the amygdala (CeA) and paraventricular nucleus (PVN) of the hypothalamus. These brain regions play an important role in activating autonomic, behavioral, and endocrine responses to stress. This study was conducted to provide needed information concerning the acute effects of stress on CeA and PVN CRH mRNA expression. Rats were exposed to restraint stress for 1 h and brains collected after a 1-h post-stress interval. CRH mRNA expression occurring in the CeA and PVN was examined using in situ hybridization techniques. Densitometric analysis revealed that acute restraint stress produced significant increases in CRH mRNA levels in the PVN and in the rostral CeA region. In addition, the area in the rostral CeA encompassing high CRH mRNA signals increased significantly after stress. Results provide clear evidence that CRH neurons in the CeA and PVN exhibit rapid increases in CRH mRNA expression after exposure to stress. |
doi_str_mv | 10.1016/S0006-8993(98)00032-8 |
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These brain regions play an important role in activating autonomic, behavioral, and endocrine responses to stress. This study was conducted to provide needed information concerning the acute effects of stress on CeA and PVN CRH mRNA expression. Rats were exposed to restraint stress for 1 h and brains collected after a 1-h post-stress interval. CRH mRNA expression occurring in the CeA and PVN was examined using in situ hybridization techniques. Densitometric analysis revealed that acute restraint stress produced significant increases in CRH mRNA levels in the PVN and in the rostral CeA region. In addition, the area in the rostral CeA encompassing high CRH mRNA signals increased significantly after stress. Results provide clear evidence that CRH neurons in the CeA and PVN exhibit rapid increases in CRH mRNA expression after exposure to stress.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(98)00032-8</identifier><identifier>PMID: 9555067</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Amygdala ; Amygdala - cytology ; Amygdala - metabolism ; Animals ; Biological and medical sciences ; Central amygdala nucleus ; Corticotropin-releasing hormone ; Corticotropin-Releasing Hormone - genetics ; Fundamental and applied biological sciences. Psychology ; Hormones and neuropeptides. Regulation ; Hypothalamus. Hypophysis. Epiphysis. Urophysis ; In Situ Hybridization ; Male ; mRNA ; Neurons - metabolism ; Neuropeptide ; Paraventricular Hypothalamic Nucleus - cytology ; Paraventricular Hypothalamic Nucleus - metabolism ; Paraventricular nucleus ; Rats ; Rats, Sprague-Dawley ; RNA, Messenger - biosynthesis ; Stress ; Stress, Physiological - metabolism ; Time Factors ; Vertebrates: endocrinology</subject><ispartof>Brain research, 1998-03, Vol.788 (1), p.305-310</ispartof><rights>1998 Elsevier Science B.V.</rights><rights>1998 INIST-CNRS</rights><rights>Copyright 1998 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-1fd4332e854b7a0b6e52b16ebb1eb2cc46234dc7c64ac644580076241f7a73703</citedby><cites>FETCH-LOGICAL-c538t-1fd4332e854b7a0b6e52b16ebb1eb2cc46234dc7c64ac644580076241f7a73703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2224646$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9555067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hsu, David T.</creatorcontrib><creatorcontrib>Chen, Feng-Ling</creatorcontrib><creatorcontrib>Takahashi, Lorey K.</creatorcontrib><creatorcontrib>Kalin, Ned H.</creatorcontrib><title>Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>High densities of nerve cells containing corticotropin-releasing hormone (CRH) are located in the central nucleus of the amygdala (CeA) and paraventricular nucleus (PVN) of the hypothalamus. These brain regions play an important role in activating autonomic, behavioral, and endocrine responses to stress. This study was conducted to provide needed information concerning the acute effects of stress on CeA and PVN CRH mRNA expression. Rats were exposed to restraint stress for 1 h and brains collected after a 1-h post-stress interval. CRH mRNA expression occurring in the CeA and PVN was examined using in situ hybridization techniques. Densitometric analysis revealed that acute restraint stress produced significant increases in CRH mRNA levels in the PVN and in the rostral CeA region. In addition, the area in the rostral CeA encompassing high CRH mRNA signals increased significantly after stress. Results provide clear evidence that CRH neurons in the CeA and PVN exhibit rapid increases in CRH mRNA expression after exposure to stress.</description><subject>Amygdala</subject><subject>Amygdala - cytology</subject><subject>Amygdala - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Central amygdala nucleus</subject><subject>Corticotropin-releasing hormone</subject><subject>Corticotropin-Releasing Hormone - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormones and neuropeptides. Regulation</subject><subject>Hypothalamus. Hypophysis. Epiphysis. Urophysis</subject><subject>In Situ Hybridization</subject><subject>Male</subject><subject>mRNA</subject><subject>Neurons - metabolism</subject><subject>Neuropeptide</subject><subject>Paraventricular Hypothalamic Nucleus - cytology</subject><subject>Paraventricular Hypothalamic Nucleus - metabolism</subject><subject>Paraventricular nucleus</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Stress</subject><subject>Stress, Physiological - metabolism</subject><subject>Time Factors</subject><subject>Vertebrates: endocrinology</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkc-O0zAQxiMEWsrCI6zkA0JwCNhO4jhcVtWKf9IKpAXO1sSebo0SO9hOpfJavCBOW3rdg2XZ32--Gc1XFFeMvmWUiXffKaWilF1Xve7km_yoeCkfFSsmW14KXtPHxeqMPC2exfhrgaqOXhQXXdM0VLSr4u8dTNaQmALGWFpnZo2G4IA7SNa7SKwj2odktU_BT9aVIYsQrbsnWx9G75CMd1_XCxcgEY0uBRgIjPt7AwMQN-sB50jAGbLdTz5t8-9oNZkgwG6hrZ4HCP_B92TtFrNo05wL-mCN_XOYJVvAsI82Pi-ebGCI-OJ0XxY_P374cfO5vP326cvN-rbUTSVTyTamriqOsqn7FmgvsOE9E9j3DHuudS14VRvdalFDPnUjKW3z4timhbZqaXVZvDr6TsH_njEmNdqocRjAoZ-jajvJpOAPg0xwIShvMtgcQR18jAE3agp2hLBXjKolVXVIVS2RqU6qQ6pK5rqrU4O5H9Gcq04xZv3lSYeoYdgEcNrGM8Y5r0UtMnZ9xDBvbWcxqKgtupy4DaiTMt4-MMg_N2XC_w</recordid><startdate>19980330</startdate><enddate>19980330</enddate><creator>Hsu, David T.</creator><creator>Chen, Feng-Ling</creator><creator>Takahashi, Lorey K.</creator><creator>Kalin, Ned H.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19980330</creationdate><title>Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis</title><author>Hsu, David T. ; Chen, Feng-Ling ; Takahashi, Lorey K. ; Kalin, Ned H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-1fd4332e854b7a0b6e52b16ebb1eb2cc46234dc7c64ac644580076241f7a73703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Amygdala</topic><topic>Amygdala - cytology</topic><topic>Amygdala - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Central amygdala nucleus</topic><topic>Corticotropin-releasing hormone</topic><topic>Corticotropin-Releasing Hormone - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormones and neuropeptides. Regulation</topic><topic>Hypothalamus. Hypophysis. Epiphysis. Urophysis</topic><topic>In Situ Hybridization</topic><topic>Male</topic><topic>mRNA</topic><topic>Neurons - metabolism</topic><topic>Neuropeptide</topic><topic>Paraventricular Hypothalamic Nucleus - cytology</topic><topic>Paraventricular Hypothalamic Nucleus - metabolism</topic><topic>Paraventricular nucleus</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Stress</topic><topic>Stress, Physiological - metabolism</topic><topic>Time Factors</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hsu, David T.</creatorcontrib><creatorcontrib>Chen, Feng-Ling</creatorcontrib><creatorcontrib>Takahashi, Lorey K.</creatorcontrib><creatorcontrib>Kalin, Ned H.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hsu, David T.</au><au>Chen, Feng-Ling</au><au>Takahashi, Lorey K.</au><au>Kalin, Ned H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1998-03-30</date><risdate>1998</risdate><volume>788</volume><issue>1</issue><spage>305</spage><epage>310</epage><pages>305-310</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>High densities of nerve cells containing corticotropin-releasing hormone (CRH) are located in the central nucleus of the amygdala (CeA) and paraventricular nucleus (PVN) of the hypothalamus. These brain regions play an important role in activating autonomic, behavioral, and endocrine responses to stress. This study was conducted to provide needed information concerning the acute effects of stress on CeA and PVN CRH mRNA expression. Rats were exposed to restraint stress for 1 h and brains collected after a 1-h post-stress interval. CRH mRNA expression occurring in the CeA and PVN was examined using in situ hybridization techniques. Densitometric analysis revealed that acute restraint stress produced significant increases in CRH mRNA levels in the PVN and in the rostral CeA region. In addition, the area in the rostral CeA encompassing high CRH mRNA signals increased significantly after stress. Results provide clear evidence that CRH neurons in the CeA and PVN exhibit rapid increases in CRH mRNA expression after exposure to stress.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>9555067</pmid><doi>10.1016/S0006-8993(98)00032-8</doi><tpages>6</tpages></addata></record> |
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subjects | Amygdala Amygdala - cytology Amygdala - metabolism Animals Biological and medical sciences Central amygdala nucleus Corticotropin-releasing hormone Corticotropin-Releasing Hormone - genetics Fundamental and applied biological sciences. Psychology Hormones and neuropeptides. Regulation Hypothalamus. Hypophysis. Epiphysis. Urophysis In Situ Hybridization Male mRNA Neurons - metabolism Neuropeptide Paraventricular Hypothalamic Nucleus - cytology Paraventricular Hypothalamic Nucleus - metabolism Paraventricular nucleus Rats Rats, Sprague-Dawley RNA, Messenger - biosynthesis Stress Stress, Physiological - metabolism Time Factors Vertebrates: endocrinology |
title | Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis |
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