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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75537
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dc.contributor.authorNagai, Michelly M.-
dc.contributor.authorGomes, Felipe V.-
dc.contributor.authorCrestani, Carlos Cesar-
dc.contributor.authorResstel, Leonardo B.M.-
dc.contributor.authorJoca, Sâmia R.L.-
dc.date.accessioned2014-05-27T11:29:35Z-
dc.date.accessioned2016-10-25T18:48:59Z-
dc.date.available2014-05-27T11:29:35Z-
dc.date.available2016-10-25T18:48:59Z-
dc.date.issued2013-06-01-
dc.identifierhttp://dx.doi.org/10.1097/FBP.0b013e3283618ae4-
dc.identifier.citationBehavioural Pharmacology, v. 24, n. 3, p. 214-221, 2013.-
dc.identifier.issn0955-8810-
dc.identifier.issn1473-5849-
dc.identifier.urihttp://hdl.handle.net/11449/75537-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75537-
dc.description.abstractThe bed nucleus of the stria terminalis (BNST) is a limbic structure that has a direct influence on the autonomic, neuroendocrine, and behavioral responses to stress. It was recently reported that reversible inactivation of synaptic transmission within this structure causes antidepressant-like effects, indicating that activation of the BNST during stressful situations would facilitate the development of behavioral changes related to the neurobiology of depression. Moreover, noradrenergic neurotransmission is abundant in the BNST and has an important role in the regulation of emotional processes related to the stress response. Thus, this study aimed to test the hypothesis that activation of adrenoceptors within the BNST facilitates the development of behavioral consequences of stress. To investigate this hypothesis, male Wistar rats were stressed (forced swimming, 15 min) and 24 h later received intra-BNST injections of vehicle, WB4101, RX821002, CGP20712, or ICI118,551, which are selective α1, α2, β1, and β2 adrenoceptor antagonists, respectively, 10 min before a 5-min forced swimming test. It was observed that administration of WB4101 (10 and 15 nmol), CGP20712 (5 and 10 nmol), or ICI118,551 (5 nmol) into the BNST reduced the immobility time of rats subjected to forced swimming test, indicating an antidepressant-like effect. These findings suggest that activation of α1, β1, and β2 adrenoceptors in the BNST could be involved in the development of the behavioral consequences of stress. © 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins.en
dc.format.extent214-221-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectadrenoceptors-
dc.subjectbed nucleus of the stria terminalis-
dc.subjectforced swimming test-
dc.subjectnoradrenaline-
dc.subjectrat-
dc.subjectstress-
dc.subject2 (2 methoxy 1,4 benzodioxan 2 yl) 2 imidazoline-
dc.subject2 [[2 (2,6 dimethoxyphenoxy)ethyl]aminomethyl] 1,4 benzodioxan-
dc.subject3 isopropylamino 1 (7 methyl 4 indanyloxy) 2 butanol-
dc.subject5 [2 [[2 hydroxy 3 [4 (1 methyl 4 trifluoromethyl 2 imidazolyl)phenoxy]propyl]amino]ethoxy]salicylamide-
dc.subjectbeta 1 adrenergic receptor-
dc.subjectbeta 2 adrenergic receptor-
dc.subjectanimal experiment-
dc.subjectanimal tissue-
dc.subjectantidepressant activity-
dc.subjectbehavior change-
dc.subjectcontrolled study-
dc.subjectimmobilization-
dc.subjectlimbic system-
dc.subjectlocomotion-
dc.subjectmale-
dc.subjectneurotransmission-
dc.subjectnonhuman-
dc.subjectnoradrenergic system-
dc.subjectopen field test-
dc.subjectstria terminalis-
dc.titleNoradrenergic neurotransmission within the bed nucleus of the stria terminalis modulates the retention of immobility in the rat forced swimming testen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Physics and Chemistry School of Pharmaceutical Sciences University of São Paulo, 14040-903, Ribeirão Preto, São Paulo-
dc.description.affiliationDepartment of Pharmacology School of Medicine University of São Paulo, Ribeirão Preto-
dc.description.affiliationLaboratory of Pharmacology Department of Natural Active Principles and Toxicology São Paulo State University, Araraquara, São Paulo-
dc.description.affiliationUnespLaboratory of Pharmacology Department of Natural Active Principles and Toxicology São Paulo State University, Araraquara, São Paulo-
dc.identifier.doi10.1097/FBP.0b013e3283618ae4-
dc.identifier.wosWOS:000318267400007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBehavioural Pharmacology-
dc.identifier.scopus2-s2.0-84876996238-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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