Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats
•Adolescent stress shapes adult behavior, physiology and neuronal activation to stress.•Effects are different within each sex.•Males had heightened emotional reactivity and reduction of neuronal excitation to stress.•Females developed a passive coping strategy and enhanced HPA axis stress reactivity...
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creator | Cotella, Evelin M. Morano, Rachel L. Wulsin, Aynara C. Martelle, Susan M. Lemen, Paige Fitzgerald, Maureen Packard, Benjamin A. Moloney, Rachel D. Herman, James P. |
description | •Adolescent stress shapes adult behavior, physiology and neuronal activation to stress.•Effects are different within each sex.•Males had heightened emotional reactivity and reduction of neuronal excitation to stress.•Females developed a passive coping strategy and enhanced HPA axis stress reactivity.•The glucocorticoid receptor modulator CORT108297 only prevented some of these effects.
Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively.
Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. In summary, our data suggest that adolescent stress differentially affects emotional behavior and circuit development in males and females, and that GR manipulation during stress can reverse at least some of these effects. |
doi_str_mv | 10.1016/j.psyneuen.2019.104490 |
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Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively.
Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. In summary, our data suggest that adolescent stress differentially affects emotional behavior and circuit development in males and females, and that GR manipulation during stress can reverse at least some of these effects.</description><identifier>ISSN: 0306-4530</identifier><identifier>EISSN: 1873-3360</identifier><identifier>DOI: 10.1016/j.psyneuen.2019.104490</identifier><identifier>PMID: 31786480</identifier><language>eng</language><publisher>OXFORD: Elsevier Ltd</publisher><subject><![CDATA[Adaptation, Psychological - drug effects ; Adaptation, Psychological - physiology ; Adolescence ; Age Factors ; Animals ; Aza Compounds - administration & dosage ; Aza Compounds - pharmacology ; Behavior, Animal - drug effects ; Behavior, Animal - physiology ; Chronic stress ; CORT108297 ; Endocrinology & Metabolism ; Female ; Glucocorticoid receptor ; Heterocyclic Compounds, 4 or More Rings - administration & dosage ; Heterocyclic Compounds, 4 or More Rings - pharmacology ; HPA axis ; Hypothalamo-Hypophyseal System - metabolism ; Hypothalamo-Hypophyseal System - physiopathology ; Life Sciences & Biomedicine ; Male ; Neurosciences ; Neurosciences & Neurology ; Psychiatry ; Rats ; Rats, Sprague-Dawley ; Receptors, Glucocorticoid - drug effects ; Receptors, Glucocorticoid - physiology ; Science & Technology ; Sex Factors ; Signal Transduction - drug effects ; Signal Transduction - physiology ; Stress, Psychological - metabolism ; Stress, Psychological - physiopathology]]></subject><ispartof>Psychoneuroendocrinology, 2020-02, Vol.112, p.104490-104490, Article 104490</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>14</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000509615800016</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c471t-ac99bcbfaed7ba9c0f123cd5723201ed7c156b9e94b15c607449a60f64a3c99d3</citedby><cites>FETCH-LOGICAL-c471t-ac99bcbfaed7ba9c0f123cd5723201ed7c156b9e94b15c607449a60f64a3c99d3</cites><orcidid>0000-0002-1774-0385 ; 0000-0001-7111-3414 ; 0000-0002-4501-6845 ; 0000-0002-7909-4008</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.psyneuen.2019.104490$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,782,786,887,3554,27933,27934,28257,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31786480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cotella, Evelin M.</creatorcontrib><creatorcontrib>Morano, Rachel L.</creatorcontrib><creatorcontrib>Wulsin, Aynara C.</creatorcontrib><creatorcontrib>Martelle, Susan M.</creatorcontrib><creatorcontrib>Lemen, Paige</creatorcontrib><creatorcontrib>Fitzgerald, Maureen</creatorcontrib><creatorcontrib>Packard, Benjamin A.</creatorcontrib><creatorcontrib>Moloney, Rachel D.</creatorcontrib><creatorcontrib>Herman, James P.</creatorcontrib><title>Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats</title><title>Psychoneuroendocrinology</title><addtitle>PSYCHONEUROENDOCRINO</addtitle><addtitle>Psychoneuroendocrinology</addtitle><description>•Adolescent stress shapes adult behavior, physiology and neuronal activation to stress.•Effects are different within each sex.•Males had heightened emotional reactivity and reduction of neuronal excitation to stress.•Females developed a passive coping strategy and enhanced HPA axis stress reactivity.•The glucocorticoid receptor modulator CORT108297 only prevented some of these effects.
Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively.
Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. In summary, our data suggest that adolescent stress differentially affects emotional behavior and circuit development in males and females, and that GR manipulation during stress can reverse at least some of these effects.</description><subject>Adaptation, Psychological - drug effects</subject><subject>Adaptation, Psychological - physiology</subject><subject>Adolescence</subject><subject>Age Factors</subject><subject>Animals</subject><subject>Aza Compounds - administration & dosage</subject><subject>Aza Compounds - pharmacology</subject><subject>Behavior, Animal - drug effects</subject><subject>Behavior, Animal - physiology</subject><subject>Chronic stress</subject><subject>CORT108297</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>Glucocorticoid receptor</subject><subject>Heterocyclic Compounds, 4 or More Rings - administration & dosage</subject><subject>Heterocyclic Compounds, 4 or More Rings - pharmacology</subject><subject>HPA axis</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Hypothalamo-Hypophyseal System - physiopathology</subject><subject>Life Sciences & Biomedicine</subject><subject>Male</subject><subject>Neurosciences</subject><subject>Neurosciences & Neurology</subject><subject>Psychiatry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Glucocorticoid - drug effects</subject><subject>Receptors, Glucocorticoid - physiology</subject><subject>Science & Technology</subject><subject>Sex Factors</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - physiology</subject><subject>Stress, Psychological - metabolism</subject><subject>Stress, Psychological - physiopathology</subject><issn>0306-4530</issn><issn>1873-3360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkctu1DAUhi0EokPhFSovkVCmdpw48QZRRfQiTYXUwtpynJPWo8QebGdQ3x6nmY5gBSsfHf__uX0InVGypoTy8-16F54sTGDXOaEiJYtCkFdoReuKZYxx8hqtCCM8K0pGTtC7ELaEEF7z_C06YbSqeVGTFYobFaKxD_hm3Ckdsetx8-idNRpfdG6AoMFGfB89hICV7fDVMGmnnY9GO9PhO9Cwi87jexhAR7MHfOu6aVDROIuNxbdqgGfjJYxzeKdieI_e9GoI8OHwnqIfl1-_N9fZ5tvVTXOxyXRR0ZgpLUSr215BV7VKaNLTnOmurHKWdk5JTUveChBFS0vNSZVOoDjpeaFYsnbsFH1e6u6mdoRuXsWrQe68GZV_kk4Z-fePNY_ywe1lxQSthEgFPh4KePdzghDlaNJFhkFZcFOQ8yC8yBmpkpQvUu1dCB76YxtK5IxMbuULMjkjkwuyZDz7c8ij7YVREtSL4Be0rg_agNVwlCWoJRGclnWKKG9MfD594yYbk_XT_1uT-suihsRkb8DLg6MzPrGVnTP_WuY32tDPGw</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Cotella, Evelin M.</creator><creator>Morano, Rachel L.</creator><creator>Wulsin, Aynara C.</creator><creator>Martelle, Susan M.</creator><creator>Lemen, Paige</creator><creator>Fitzgerald, Maureen</creator><creator>Packard, Benjamin A.</creator><creator>Moloney, Rachel D.</creator><creator>Herman, James P.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</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>5PM</scope><orcidid>https://orcid.org/0000-0002-1774-0385</orcidid><orcidid>https://orcid.org/0000-0001-7111-3414</orcidid><orcidid>https://orcid.org/0000-0002-4501-6845</orcidid><orcidid>https://orcid.org/0000-0002-7909-4008</orcidid></search><sort><creationdate>20200201</creationdate><title>Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats</title><author>Cotella, Evelin M. ; 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Adolescent animals are vulnerable to the effects of stress on brain development. We hypothesized that long-term effects of adolescent chronic stress are mediated by glucocorticoid receptor (GR) signaling. We used a specific GR modulator (CORT108297) to pharmacologically disrupt GR signaling in adolescent rats during exposure to chronic variable stress (CVS). Male and female rats received 30 mg/kg of drug during a 2-week CVS protocol starting at PND46. Emotional reactivity (open field) and coping behaviors (forced swim test (FST)) were then tested in adulthood, 5 weeks after the end of the CVS protocol. Blood samples were collected two days before FST and serial samples after the onset of the swim test to determine baseline and stress response levels of HPA hormones respectively.
Our results support differential behavioral, physiological and stress circuit reactivity to adolescent chronic stress exposure in males and females, with variable involvement of GR signaling. In response to adolescent stress, males had heightened reactivity to novelty and exhibited marked reduction in neuronal excitation following swim stress in adulthood, whereas females developed a passive coping strategy in the FST and enhanced HPA axis stress reactivity. Only the latter effect was attenuated by treatment with the GR modulator C108297. In summary, our data suggest that adolescent stress differentially affects emotional behavior and circuit development in males and females, and that GR manipulation during stress can reverse at least some of these effects.</abstract><cop>OXFORD</cop><pub>Elsevier Ltd</pub><pmid>31786480</pmid><doi>10.1016/j.psyneuen.2019.104490</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-1774-0385</orcidid><orcidid>https://orcid.org/0000-0001-7111-3414</orcidid><orcidid>https://orcid.org/0000-0002-4501-6845</orcidid><orcidid>https://orcid.org/0000-0002-7909-4008</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation, Psychological - drug effects Adaptation, Psychological - physiology Adolescence Age Factors Animals Aza Compounds - administration & dosage Aza Compounds - pharmacology Behavior, Animal - drug effects Behavior, Animal - physiology Chronic stress CORT108297 Endocrinology & Metabolism Female Glucocorticoid receptor Heterocyclic Compounds, 4 or More Rings - administration & dosage Heterocyclic Compounds, 4 or More Rings - pharmacology HPA axis Hypothalamo-Hypophyseal System - metabolism Hypothalamo-Hypophyseal System - physiopathology Life Sciences & Biomedicine Male Neurosciences Neurosciences & Neurology Psychiatry Rats Rats, Sprague-Dawley Receptors, Glucocorticoid - drug effects Receptors, Glucocorticoid - physiology Science & Technology Sex Factors Signal Transduction - drug effects Signal Transduction - physiology Stress, Psychological - metabolism Stress, Psychological - physiopathology |
title | Lasting Impact of Chronic Adolescent Stress and Glucocorticoid Receptor Selective Modulation in Male and Female Rats |
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