Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice

The corticotropin-releasing hormone (CRH) and its cognate receptors have been implicated in the pathophysiology of stress-related disorders. Hypersecretion of central CRH and elevated glucocorticoid levels, as a consequence of impaired feedback control, have been shown to accompany mood and anxiety...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cellular and molecular neurobiology 2012-07, Vol.32 (5), p.815-828
Hauptverfasser: Dedic, Nina, Touma, Chadi, Romanowski, Cristoph P., Schieven, Marcel, Kühne, Claudia, Ableitner, Martin, Lu, Ailing, Holsboer, Florian, Wurst, Wolfgang, Kimura, Mayumi, Deussing, Jan M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 828
container_issue 5
container_start_page 815
container_title Cellular and molecular neurobiology
container_volume 32
creator Dedic, Nina
Touma, Chadi
Romanowski, Cristoph P.
Schieven, Marcel
Kühne, Claudia
Ableitner, Martin
Lu, Ailing
Holsboer, Florian
Wurst, Wolfgang
Kimura, Mayumi
Deussing, Jan M.
description The corticotropin-releasing hormone (CRH) and its cognate receptors have been implicated in the pathophysiology of stress-related disorders. Hypersecretion of central CRH and elevated glucocorticoid levels, as a consequence of impaired feedback control, have been shown to accompany mood and anxiety disorders. However, a clear discrimination of direct effects of centrally hypersecreted CRH from those resulting from HPA axis activation has been difficult. Applying a conditional strategy, we have generated two conditional CRH-overexpressing mouse lines: CRH - COE Del mice overexpress CRH throughout the body, while CRH - COE APit mice selectively overexpress CRH in the anterior and intermediate lobe of the pituitary. Both mouse lines show increased basal plasma corticosterone levels and consequently develop signs of Cushing’s syndrome. However, while mice ubiquitously overexpressing CRH exhibited increased anxiety-related behaviour, overexpression of CRH in the pituitary did not produce alterations in emotional behaviour. These results suggest that chronic hypercorticosteroidism alone is not sufficient to alter anxiety-related behaviour but rather that central CRH hyperdrive on its own or in combination with elevated glucocorticoids is responsible for the increase in anxiety-related behaviour. In conclusion, the generated mouse lines represent valuable animal models to study the consequences of chronic CRH overproduction and HPA axis activation.
doi_str_mv 10.1007/s10571-011-9784-0
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1021256889</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1021256889</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-9c6576ea58c88576c5cfd4ce18a89231904945a620b1f28fe0ffe6f2c29178f43</originalsourceid><addsrcrecordid>eNp9kE1PAyEQhonRaP34AV7MHr2gAwu7cFw3ak00GqNnghQU0-5WZtvov5fa6tHTMOF530weQo4ZnDGA-hwZyJpRYIzqWgkKW2TEZF3SSpWwTUbAa05FKWCP7CO-A4AGkLtkj3OmlZT1iIQG0SPG7rW48G92GftFstPiMgTvBiz6ULRvqe-iK8YPTdF8RiwaN8SlHWLfFc8_wbbvJnG152D7OKb3S5_85zxteu-i84dkJ9gp-qPNPCDPV5dP7Zje3l_ftM0tdaUQA9WuknXlrVROqfxy0oWJcJ4pqzQvmQahhbQVhxcWuAoe8p1V4I5rVqsgygNyuu6dp_5j4XEws4jOT6e28_0CDQPOuKyU0hlla9SlHjH5YOYpzmz6ypBZ6TVrvSbrNSu9BnLmZFO_eJn5yV_i12cG-BrA_NW9-mTes9AsBv9p_QaqXYUD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1021256889</pqid></control><display><type>article</type><title>Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice</title><source>MEDLINE</source><source>SpringerLink (Online service)</source><creator>Dedic, Nina ; Touma, Chadi ; Romanowski, Cristoph P. ; Schieven, Marcel ; Kühne, Claudia ; Ableitner, Martin ; Lu, Ailing ; Holsboer, Florian ; Wurst, Wolfgang ; Kimura, Mayumi ; Deussing, Jan M.</creator><creatorcontrib>Dedic, Nina ; Touma, Chadi ; Romanowski, Cristoph P. ; Schieven, Marcel ; Kühne, Claudia ; Ableitner, Martin ; Lu, Ailing ; Holsboer, Florian ; Wurst, Wolfgang ; Kimura, Mayumi ; Deussing, Jan M.</creatorcontrib><description>The corticotropin-releasing hormone (CRH) and its cognate receptors have been implicated in the pathophysiology of stress-related disorders. Hypersecretion of central CRH and elevated glucocorticoid levels, as a consequence of impaired feedback control, have been shown to accompany mood and anxiety disorders. However, a clear discrimination of direct effects of centrally hypersecreted CRH from those resulting from HPA axis activation has been difficult. Applying a conditional strategy, we have generated two conditional CRH-overexpressing mouse lines: CRH - COE Del mice overexpress CRH throughout the body, while CRH - COE APit mice selectively overexpress CRH in the anterior and intermediate lobe of the pituitary. Both mouse lines show increased basal plasma corticosterone levels and consequently develop signs of Cushing’s syndrome. However, while mice ubiquitously overexpressing CRH exhibited increased anxiety-related behaviour, overexpression of CRH in the pituitary did not produce alterations in emotional behaviour. These results suggest that chronic hypercorticosteroidism alone is not sufficient to alter anxiety-related behaviour but rather that central CRH hyperdrive on its own or in combination with elevated glucocorticoids is responsible for the increase in anxiety-related behaviour. In conclusion, the generated mouse lines represent valuable animal models to study the consequences of chronic CRH overproduction and HPA axis activation.</description><identifier>ISSN: 0272-4340</identifier><identifier>ISSN: 1573-6830</identifier><identifier>EISSN: 1573-6830</identifier><identifier>DOI: 10.1007/s10571-011-9784-0</identifier><identifier>PMID: 22198557</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Anxiety - metabolism ; Anxiety - pathology ; Behavior, Animal - physiology ; Biomedical and Life Sciences ; Biomedicine ; Cell Biology ; Corticotropin-Releasing Hormone - metabolism ; Female ; Hypothalamo-Hypophyseal System - metabolism ; Hypothalamo-Hypophyseal System - pathology ; Male ; Mice ; Mice, Transgenic ; Neurobiology ; Neurosciences ; Organ Specificity ; Original Paper ; Pituitary Gland - metabolism ; Pituitary-Adrenal System - metabolism ; Pituitary-Adrenal System - pathology ; Sleep, REM</subject><ispartof>Cellular and molecular neurobiology, 2012-07, Vol.32 (5), p.815-828</ispartof><rights>Springer Science+Business Media, LLC 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-9c6576ea58c88576c5cfd4ce18a89231904945a620b1f28fe0ffe6f2c29178f43</citedby><cites>FETCH-LOGICAL-c344t-9c6576ea58c88576c5cfd4ce18a89231904945a620b1f28fe0ffe6f2c29178f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10571-011-9784-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10571-011-9784-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22198557$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dedic, Nina</creatorcontrib><creatorcontrib>Touma, Chadi</creatorcontrib><creatorcontrib>Romanowski, Cristoph P.</creatorcontrib><creatorcontrib>Schieven, Marcel</creatorcontrib><creatorcontrib>Kühne, Claudia</creatorcontrib><creatorcontrib>Ableitner, Martin</creatorcontrib><creatorcontrib>Lu, Ailing</creatorcontrib><creatorcontrib>Holsboer, Florian</creatorcontrib><creatorcontrib>Wurst, Wolfgang</creatorcontrib><creatorcontrib>Kimura, Mayumi</creatorcontrib><creatorcontrib>Deussing, Jan M.</creatorcontrib><title>Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice</title><title>Cellular and molecular neurobiology</title><addtitle>Cell Mol Neurobiol</addtitle><addtitle>Cell Mol Neurobiol</addtitle><description>The corticotropin-releasing hormone (CRH) and its cognate receptors have been implicated in the pathophysiology of stress-related disorders. Hypersecretion of central CRH and elevated glucocorticoid levels, as a consequence of impaired feedback control, have been shown to accompany mood and anxiety disorders. However, a clear discrimination of direct effects of centrally hypersecreted CRH from those resulting from HPA axis activation has been difficult. Applying a conditional strategy, we have generated two conditional CRH-overexpressing mouse lines: CRH - COE Del mice overexpress CRH throughout the body, while CRH - COE APit mice selectively overexpress CRH in the anterior and intermediate lobe of the pituitary. Both mouse lines show increased basal plasma corticosterone levels and consequently develop signs of Cushing’s syndrome. However, while mice ubiquitously overexpressing CRH exhibited increased anxiety-related behaviour, overexpression of CRH in the pituitary did not produce alterations in emotional behaviour. These results suggest that chronic hypercorticosteroidism alone is not sufficient to alter anxiety-related behaviour but rather that central CRH hyperdrive on its own or in combination with elevated glucocorticoids is responsible for the increase in anxiety-related behaviour. In conclusion, the generated mouse lines represent valuable animal models to study the consequences of chronic CRH overproduction and HPA axis activation.</description><subject>Animals</subject><subject>Anxiety - metabolism</subject><subject>Anxiety - pathology</subject><subject>Behavior, Animal - physiology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Biology</subject><subject>Corticotropin-Releasing Hormone - metabolism</subject><subject>Female</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Hypothalamo-Hypophyseal System - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Neurobiology</subject><subject>Neurosciences</subject><subject>Organ Specificity</subject><subject>Original Paper</subject><subject>Pituitary Gland - metabolism</subject><subject>Pituitary-Adrenal System - metabolism</subject><subject>Pituitary-Adrenal System - pathology</subject><subject>Sleep, REM</subject><issn>0272-4340</issn><issn>1573-6830</issn><issn>1573-6830</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PAyEQhonRaP34AV7MHr2gAwu7cFw3ak00GqNnghQU0-5WZtvov5fa6tHTMOF530weQo4ZnDGA-hwZyJpRYIzqWgkKW2TEZF3SSpWwTUbAa05FKWCP7CO-A4AGkLtkj3OmlZT1iIQG0SPG7rW48G92GftFstPiMgTvBiz6ULRvqe-iK8YPTdF8RiwaN8SlHWLfFc8_wbbvJnG152D7OKb3S5_85zxteu-i84dkJ9gp-qPNPCDPV5dP7Zje3l_ftM0tdaUQA9WuknXlrVROqfxy0oWJcJ4pqzQvmQahhbQVhxcWuAoe8p1V4I5rVqsgygNyuu6dp_5j4XEws4jOT6e28_0CDQPOuKyU0hlla9SlHjH5YOYpzmz6ypBZ6TVrvSbrNSu9BnLmZFO_eJn5yV_i12cG-BrA_NW9-mTes9AsBv9p_QaqXYUD</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Dedic, Nina</creator><creator>Touma, Chadi</creator><creator>Romanowski, Cristoph P.</creator><creator>Schieven, Marcel</creator><creator>Kühne, Claudia</creator><creator>Ableitner, Martin</creator><creator>Lu, Ailing</creator><creator>Holsboer, Florian</creator><creator>Wurst, Wolfgang</creator><creator>Kimura, Mayumi</creator><creator>Deussing, Jan M.</creator><general>Springer US</general><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>7X8</scope></search><sort><creationdate>20120701</creationdate><title>Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice</title><author>Dedic, Nina ; Touma, Chadi ; Romanowski, Cristoph P. ; Schieven, Marcel ; Kühne, Claudia ; Ableitner, Martin ; Lu, Ailing ; Holsboer, Florian ; Wurst, Wolfgang ; Kimura, Mayumi ; Deussing, Jan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-9c6576ea58c88576c5cfd4ce18a89231904945a620b1f28fe0ffe6f2c29178f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Anxiety - metabolism</topic><topic>Anxiety - pathology</topic><topic>Behavior, Animal - physiology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Biology</topic><topic>Corticotropin-Releasing Hormone - metabolism</topic><topic>Female</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Hypothalamo-Hypophyseal System - pathology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Neurobiology</topic><topic>Neurosciences</topic><topic>Organ Specificity</topic><topic>Original Paper</topic><topic>Pituitary Gland - metabolism</topic><topic>Pituitary-Adrenal System - metabolism</topic><topic>Pituitary-Adrenal System - pathology</topic><topic>Sleep, REM</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dedic, Nina</creatorcontrib><creatorcontrib>Touma, Chadi</creatorcontrib><creatorcontrib>Romanowski, Cristoph P.</creatorcontrib><creatorcontrib>Schieven, Marcel</creatorcontrib><creatorcontrib>Kühne, Claudia</creatorcontrib><creatorcontrib>Ableitner, Martin</creatorcontrib><creatorcontrib>Lu, Ailing</creatorcontrib><creatorcontrib>Holsboer, Florian</creatorcontrib><creatorcontrib>Wurst, Wolfgang</creatorcontrib><creatorcontrib>Kimura, Mayumi</creatorcontrib><creatorcontrib>Deussing, Jan M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular and molecular neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dedic, Nina</au><au>Touma, Chadi</au><au>Romanowski, Cristoph P.</au><au>Schieven, Marcel</au><au>Kühne, Claudia</au><au>Ableitner, Martin</au><au>Lu, Ailing</au><au>Holsboer, Florian</au><au>Wurst, Wolfgang</au><au>Kimura, Mayumi</au><au>Deussing, Jan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice</atitle><jtitle>Cellular and molecular neurobiology</jtitle><stitle>Cell Mol Neurobiol</stitle><addtitle>Cell Mol Neurobiol</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>32</volume><issue>5</issue><spage>815</spage><epage>828</epage><pages>815-828</pages><issn>0272-4340</issn><issn>1573-6830</issn><eissn>1573-6830</eissn><abstract>The corticotropin-releasing hormone (CRH) and its cognate receptors have been implicated in the pathophysiology of stress-related disorders. Hypersecretion of central CRH and elevated glucocorticoid levels, as a consequence of impaired feedback control, have been shown to accompany mood and anxiety disorders. However, a clear discrimination of direct effects of centrally hypersecreted CRH from those resulting from HPA axis activation has been difficult. Applying a conditional strategy, we have generated two conditional CRH-overexpressing mouse lines: CRH - COE Del mice overexpress CRH throughout the body, while CRH - COE APit mice selectively overexpress CRH in the anterior and intermediate lobe of the pituitary. Both mouse lines show increased basal plasma corticosterone levels and consequently develop signs of Cushing’s syndrome. However, while mice ubiquitously overexpressing CRH exhibited increased anxiety-related behaviour, overexpression of CRH in the pituitary did not produce alterations in emotional behaviour. These results suggest that chronic hypercorticosteroidism alone is not sufficient to alter anxiety-related behaviour but rather that central CRH hyperdrive on its own or in combination with elevated glucocorticoids is responsible for the increase in anxiety-related behaviour. In conclusion, the generated mouse lines represent valuable animal models to study the consequences of chronic CRH overproduction and HPA axis activation.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>22198557</pmid><doi>10.1007/s10571-011-9784-0</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0272-4340
ispartof Cellular and molecular neurobiology, 2012-07, Vol.32 (5), p.815-828
issn 0272-4340
1573-6830
1573-6830
language eng
recordid cdi_proquest_miscellaneous_1021256889
source MEDLINE; SpringerLink (Online service)
subjects Animals
Anxiety - metabolism
Anxiety - pathology
Behavior, Animal - physiology
Biomedical and Life Sciences
Biomedicine
Cell Biology
Corticotropin-Releasing Hormone - metabolism
Female
Hypothalamo-Hypophyseal System - metabolism
Hypothalamo-Hypophyseal System - pathology
Male
Mice
Mice, Transgenic
Neurobiology
Neurosciences
Organ Specificity
Original Paper
Pituitary Gland - metabolism
Pituitary-Adrenal System - metabolism
Pituitary-Adrenal System - pathology
Sleep, REM
title Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T08%3A07%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Assessing%20Behavioural%20Effects%20of%20Chronic%20HPA%20Axis%20Activation%20Using%20Conditional%20CRH-Overexpressing%20Mice&rft.jtitle=Cellular%20and%20molecular%20neurobiology&rft.au=Dedic,%20Nina&rft.date=2012-07-01&rft.volume=32&rft.issue=5&rft.spage=815&rft.epage=828&rft.pages=815-828&rft.issn=0272-4340&rft.eissn=1573-6830&rft_id=info:doi/10.1007/s10571-011-9784-0&rft_dat=%3Cproquest_cross%3E1021256889%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1021256889&rft_id=info:pmid/22198557&rfr_iscdi=true