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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/129403
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dc.contributor.authorDuarte, Josiane O.-
dc.contributor.authorCruz, Fabio C.-
dc.contributor.authorLeao, Rodrigo M.-
dc.contributor.authorPlaneta, Cleopatra S.-
dc.contributor.authorCrestani, Carlos C.-
dc.date.accessioned2015-10-21T21:01:23Z-
dc.date.accessioned2016-10-25T21:09:06Z-
dc.date.available2015-10-21T21:01:23Z-
dc.date.available2016-10-25T21:09:06Z-
dc.date.issued2015-02-01-
dc.identifierhttp://journals.lww.com/psychosomaticmedicine/pages/articleviewer.aspx?year=2015&issue=02000&article=00010&type=abstract-
dc.identifier.citationPsychosomatic Medicine. Philadelphia: Lippincott Williams &wilkins, v. 77, n. 2, p. 186-199, 2015.-
dc.identifier.issn0033-3174-
dc.identifier.urihttp://hdl.handle.net/11449/129403-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/129403-
dc.description.abstractObjective This study investigated the physiological and somatic changes evoked by daily exposure to the same type of stressor (homotypic) or different aversive stressor stimuli (heterotypic) in adolescent and adult rats, with a focus on cardiovascular function. The long-term effects of stress exposure during adolescence were also investigated longitudinally.Methods Male Wistar rats were exposed to repeated restraint stress (RRS, homotypic) or chronic variable stress (CVS, heterotypic).Results Adrenal hypertrophy, thymus involution, and elevated plasma glucocorticoid were observed only in adolescent animals, whereas reduction in body weight was caused by both stress regimens in adults. CVS increased mean arterial pressure (adolescent: p = .001; adult: p = .005) and heart rate (HR; adolescent: p = .020; adult: p = .011) regardless of the age, whereas RRS increased blood pressure selectively in adults (p = .001). Rest tachycardia evoked by CVS was associated with increased cardiac sympathetic activity in adults, whereas a decreased cardiac parasympathetic activity was observed in adolescent animals. Changes in cardiovascular function and cardiac autonomic activity evoked by both CVS and RRS were followed by alterations in baroreflex activity and vascular reactivity to vasoconstrictor and vasodilator agents in adolescent adult animals. Except for the circulating glucocorticoid change, all alterations observed during adolescence were reversed in adulthood.Conclusions These findings suggest a stress vulnerability of adolescents to somatic and neuroendocrine effects regardless of stress regimen. Our results indicated an age-stress type-specific influence in stress-evoked cardiovascular/autonomic changes. Data suggest minimal consequences in adulthood of stress during adolescence.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipPADC-FCF UNESP-
dc.format.extent186-199-
dc.language.isoeng-
dc.publisherLippincott Williams &wilkins-
dc.sourceWeb of Science-
dc.subjectUnpredictable stressen
dc.subjectRestrainten
dc.subjectAutonomicen
dc.subjectBaroreflexen
dc.subjectVascularen
dc.subjectGlucocorticoidsen
dc.titleStress vulnerability during adolescence: comparison of chronic stressors in adolescent and adult ratsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionNIDA-
dc.description.affiliationUniv Estadual Paulista UNESP, Pharmacol Lab, Sch Pharmaceut Sci, Araraquara, SP, Brazil-
dc.description.affiliationJoint UFSCar UNESP Grad Program Physiol Sci, Sao Carlos, SP, Brazil-
dc.description.affiliationNIDA, Behav Neurosci Branch, Intramural Res Program, US Natl Inst Hlth,Dept Hlth &Human Serv, Baltimore, MD USA-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Faculdade de Ciências Farmacêuticas de Araraquara, Departamento de Princípios Ativos Naturais e Toxicologia, Pharmacol Lab, Sch Pharmaceut Sci, Araraquara, SP, Brazil-
dc.description.affiliationUnespJoint UFSCar UNESP Grad Program Physiol Sci, Sao Carlos, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 2012/14376-0-
dc.description.sponsorshipIdFAPESP: 2012/50549-6-
dc.identifier.doihttp://dx.doi.org/10.1097/PSY.0000000000000141-
dc.identifier.wosWOS:000350051500009-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPsychosomatic Medicine-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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