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...
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Veröffentlicht in: | Cellular and molecular neurobiology 2012-07, Vol.32 (5), p.815-828 |
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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 |
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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> |
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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 |
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