SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat
•Chronic social defeat during adolescence increases depressive-like behaviors in male rats.•Chronic fluoxetine attenuates the behavioral effects of chronic social defeat but also reduces body weight gain over development.•The CRF1 receptor antagonist GSK876008 attenuates the behavioral effects of ch...
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Veröffentlicht in: | Behavioural brain research 2014-08, Vol.270, p.295-299 |
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description | •Chronic social defeat during adolescence increases depressive-like behaviors in male rats.•Chronic fluoxetine attenuates the behavioral effects of chronic social defeat but also reduces body weight gain over development.•The CRF1 receptor antagonist GSK876008 attenuates the behavioral effects of chronic social defeat without causing alterations in weight gain.
Depression and anxiety during adolescence are complex disorders due to persistent effects on physiology and behavior. Selective-serotonin reuptake inhibitors (SSRI) are currently the most widely used pharmacological intervention for depression. Corticotropin-releasing factor one (CRF1) receptor antagonists represent a novel class of compounds that may have efficacy for depressive and anxiety disorders. This study used an animal model of chronic adolescent stress to determine the efficacy of the SSRI fluoxetine, and a novel CRF1 receptor antagonist, GSK876008, on prevention of the behavioral effects of chronic adolescent stress. Male rats were exposed to chronic social defeat stress, fluoxetine, and/or GSK876008 from postnatal day 28-50. Chronic stress-induced depressive-like behaviors were partially attenuated by either concurrent fluoxetine or GSK876008. Fluoxetine blunted body mass gain in the adolescents exposed to chronic stress. The collective data demonstrate similar efficacy between a SSRI and a CRF1 receptor antagonist in the attenuation of stress-induced anhedonia but fewer side effects were observed in those rats treated with the CRF1 receptor antagonist. These data suggest that CRF1 receptor antagonists may be a viable alternative for treatment of depressive behaviors in adolescents. |
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Depression and anxiety during adolescence are complex disorders due to persistent effects on physiology and behavior. Selective-serotonin reuptake inhibitors (SSRI) are currently the most widely used pharmacological intervention for depression. Corticotropin-releasing factor one (CRF1) receptor antagonists represent a novel class of compounds that may have efficacy for depressive and anxiety disorders. This study used an animal model of chronic adolescent stress to determine the efficacy of the SSRI fluoxetine, and a novel CRF1 receptor antagonist, GSK876008, on prevention of the behavioral effects of chronic adolescent stress. Male rats were exposed to chronic social defeat stress, fluoxetine, and/or GSK876008 from postnatal day 28-50. Chronic stress-induced depressive-like behaviors were partially attenuated by either concurrent fluoxetine or GSK876008. Fluoxetine blunted body mass gain in the adolescents exposed to chronic stress. The collective data demonstrate similar efficacy between a SSRI and a CRF1 receptor antagonist in the attenuation of stress-induced anhedonia but fewer side effects were observed in those rats treated with the CRF1 receptor antagonist. These data suggest that CRF1 receptor antagonists may be a viable alternative for treatment of depressive behaviors in adolescents.</description><identifier>ISSN: 0166-4328</identifier><identifier>EISSN: 1872-7549</identifier><identifier>DOI: 10.1016/j.bbr.2014.05.035</identifier><identifier>PMID: 24867331</identifier><identifier>CODEN: BBREDI</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>Adolescence ; Adult and adolescent clinical studies ; Aging - drug effects ; Aging - psychology ; Animals ; Behavior, Animal - drug effects ; Biological and medical sciences ; CRF ; Depression ; Depression - prevention & control ; Depression - psychology ; Fluoxetine - pharmacology ; Fundamental and applied biological sciences. Psychology ; Male ; Medical sciences ; Methylcellulose - analogs & derivatives ; Methylcellulose - pharmacology ; Mood disorders ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Rats ; Rats, Wistar ; Receptors, Corticotropin-Releasing Hormone - antagonists & inhibitors ; Serotonin Uptake Inhibitors - pharmacology ; Social Behavior ; SSRI ; Stress ; Stress, Psychological - complications ; Stress, Psychological - drug therapy ; Vertebrates: nervous system and sense organs</subject><ispartof>Behavioural brain research, 2014-08, Vol.270, p.295-299</ispartof><rights>2014 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-a01e7e944a488784ed55862fd71208f27108529f26bba297f36aabb08512445d3</citedby><cites>FETCH-LOGICAL-c482t-a01e7e944a488784ed55862fd71208f27108529f26bba297f36aabb08512445d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0166432814003362$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28583120$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24867331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bourke, Chase H.</creatorcontrib><creatorcontrib>Glasper, Erica R.</creatorcontrib><creatorcontrib>Neigh, Gretchen N.</creatorcontrib><title>SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat</title><title>Behavioural brain research</title><addtitle>Behav Brain Res</addtitle><description>•Chronic social defeat during adolescence increases depressive-like behaviors in male rats.•Chronic fluoxetine attenuates the behavioral effects of chronic social defeat but also reduces body weight gain over development.•The CRF1 receptor antagonist GSK876008 attenuates the behavioral effects of chronic social defeat without causing alterations in weight gain.
Depression and anxiety during adolescence are complex disorders due to persistent effects on physiology and behavior. Selective-serotonin reuptake inhibitors (SSRI) are currently the most widely used pharmacological intervention for depression. Corticotropin-releasing factor one (CRF1) receptor antagonists represent a novel class of compounds that may have efficacy for depressive and anxiety disorders. This study used an animal model of chronic adolescent stress to determine the efficacy of the SSRI fluoxetine, and a novel CRF1 receptor antagonist, GSK876008, on prevention of the behavioral effects of chronic adolescent stress. Male rats were exposed to chronic social defeat stress, fluoxetine, and/or GSK876008 from postnatal day 28-50. Chronic stress-induced depressive-like behaviors were partially attenuated by either concurrent fluoxetine or GSK876008. Fluoxetine blunted body mass gain in the adolescents exposed to chronic stress. The collective data demonstrate similar efficacy between a SSRI and a CRF1 receptor antagonist in the attenuation of stress-induced anhedonia but fewer side effects were observed in those rats treated with the CRF1 receptor antagonist. These data suggest that CRF1 receptor antagonists may be a viable alternative for treatment of depressive behaviors in adolescents.</description><subject>Adolescence</subject><subject>Adult and adolescent clinical studies</subject><subject>Aging - drug effects</subject><subject>Aging - psychology</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Biological and medical sciences</subject><subject>CRF</subject><subject>Depression</subject><subject>Depression - prevention & control</subject><subject>Depression - psychology</subject><subject>Fluoxetine - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methylcellulose - analogs & derivatives</subject><subject>Methylcellulose - pharmacology</subject><subject>Mood disorders</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Corticotropin-Releasing Hormone - antagonists & inhibitors</subject><subject>Serotonin Uptake Inhibitors - pharmacology</subject><subject>Social Behavior</subject><subject>SSRI</subject><subject>Stress</subject><subject>Stress, Psychological - complications</subject><subject>Stress, Psychological - drug therapy</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0166-4328</issn><issn>1872-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGKFDEQhoMo7rj6AF4kF8FLt0k66aTxJIOrCwvCrp5DdbqiGbs7Y5IZ2Lc3y4x600sVVH1_UVU_IS85aznj_dtdO46pFYzLlqmWdeoR2XCjRaOVHB6TTWX6RnbCXJBnOe8YY5Ip_pRcCGl63XV8Q9zd3e01jYlub68orAW-xTXkhe4hlQDzfE9hwTnEBAXphPuEOYcjNnP4gXTE73CsPQq-YI1TnDE7XAvN0VV1FXiE8pw88TBnfHHOl-Tr1Ycv20_NzeeP19v3N42TRpQGGEeNg5QgjdFG4qSU6YWfNBfMeKE5M0oMXvTjCGLQvusBxrEWuZBSTd0leXOau0_x5wFzsUuo68wzrBgP2fJe6EErzvX_USW73ihpWEX5CXUp5pzQ230KC6R7y5l9sMHubLXBPthgmbLVhqp5dR5_GBec_ih-_70Cr88AZAezT7C6kP9yRpmuXl25dycO69-OAZPNLuDqcAoJXbFTDP9Y4xeEu6Px</recordid><startdate>20140815</startdate><enddate>20140815</enddate><creator>Bourke, Chase H.</creator><creator>Glasper, Erica R.</creator><creator>Neigh, Gretchen N.</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>7X8</scope><scope>7QG</scope><scope>7TK</scope></search><sort><creationdate>20140815</creationdate><title>SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat</title><author>Bourke, Chase H. ; Glasper, Erica R. ; Neigh, Gretchen N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-a01e7e944a488784ed55862fd71208f27108529f26bba297f36aabb08512445d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescence</topic><topic>Adult and adolescent clinical studies</topic><topic>Aging - drug effects</topic><topic>Aging - psychology</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>CRF</topic><topic>Depression</topic><topic>Depression - prevention & control</topic><topic>Depression - psychology</topic><topic>Fluoxetine - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methylcellulose - analogs & derivatives</topic><topic>Methylcellulose - pharmacology</topic><topic>Mood disorders</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Corticotropin-Releasing Hormone - antagonists & inhibitors</topic><topic>Serotonin Uptake Inhibitors - pharmacology</topic><topic>Social Behavior</topic><topic>SSRI</topic><topic>Stress</topic><topic>Stress, Psychological - complications</topic><topic>Stress, Psychological - drug therapy</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bourke, Chase H.</creatorcontrib><creatorcontrib>Glasper, Erica R.</creatorcontrib><creatorcontrib>Neigh, Gretchen N.</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>MEDLINE - Academic</collection><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Behavioural brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bourke, Chase H.</au><au>Glasper, Erica R.</au><au>Neigh, Gretchen N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat</atitle><jtitle>Behavioural brain research</jtitle><addtitle>Behav Brain Res</addtitle><date>2014-08-15</date><risdate>2014</risdate><volume>270</volume><spage>295</spage><epage>299</epage><pages>295-299</pages><issn>0166-4328</issn><eissn>1872-7549</eissn><coden>BBREDI</coden><abstract>•Chronic social defeat during adolescence increases depressive-like behaviors in male rats.•Chronic fluoxetine attenuates the behavioral effects of chronic social defeat but also reduces body weight gain over development.•The CRF1 receptor antagonist GSK876008 attenuates the behavioral effects of chronic social defeat without causing alterations in weight gain.
Depression and anxiety during adolescence are complex disorders due to persistent effects on physiology and behavior. Selective-serotonin reuptake inhibitors (SSRI) are currently the most widely used pharmacological intervention for depression. Corticotropin-releasing factor one (CRF1) receptor antagonists represent a novel class of compounds that may have efficacy for depressive and anxiety disorders. This study used an animal model of chronic adolescent stress to determine the efficacy of the SSRI fluoxetine, and a novel CRF1 receptor antagonist, GSK876008, on prevention of the behavioral effects of chronic adolescent stress. Male rats were exposed to chronic social defeat stress, fluoxetine, and/or GSK876008 from postnatal day 28-50. Chronic stress-induced depressive-like behaviors were partially attenuated by either concurrent fluoxetine or GSK876008. Fluoxetine blunted body mass gain in the adolescents exposed to chronic stress. The collective data demonstrate similar efficacy between a SSRI and a CRF1 receptor antagonist in the attenuation of stress-induced anhedonia but fewer side effects were observed in those rats treated with the CRF1 receptor antagonist. These data suggest that CRF1 receptor antagonists may be a viable alternative for treatment of depressive behaviors in adolescents.</abstract><cop>Shannon</cop><pub>Elsevier B.V</pub><pmid>24867331</pmid><doi>10.1016/j.bbr.2014.05.035</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescence Adult and adolescent clinical studies Aging - drug effects Aging - psychology Animals Behavior, Animal - drug effects Biological and medical sciences CRF Depression Depression - prevention & control Depression - psychology Fluoxetine - pharmacology Fundamental and applied biological sciences. Psychology Male Medical sciences Methylcellulose - analogs & derivatives Methylcellulose - pharmacology Mood disorders Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Rats Rats, Wistar Receptors, Corticotropin-Releasing Hormone - antagonists & inhibitors Serotonin Uptake Inhibitors - pharmacology Social Behavior SSRI Stress Stress, Psychological - complications Stress, Psychological - drug therapy Vertebrates: nervous system and sense organs |
title | SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat |
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