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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/74652
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dc.contributor.authorCampos, Kelciane Ferreira Caetano-
dc.contributor.authorAmaral, Vanessa Cristiane Santana-
dc.contributor.authorRico, Javier Leonardo-
dc.contributor.authorMiguel, Tarciso Tadeu-
dc.contributor.authorNunes-de-Souza, Ricardo Luiz-
dc.date.accessioned2014-05-27T11:28:33Z-
dc.date.accessioned2016-10-25T18:44:54Z-
dc.date.available2014-05-27T11:28:33Z-
dc.date.available2016-10-25T18:44:54Z-
dc.date.issued2013-03-01-
dc.identifierhttp://dx.doi.org/10.1016/j.bbr.2012.11.023-
dc.identifier.citationBehavioural Brain Research, v. 240, n. 1, p. 160-170, 2013.-
dc.identifier.issn0166-4328-
dc.identifier.issn1872-7549-
dc.identifier.urihttp://hdl.handle.net/11449/74652-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74652-
dc.description.abstractThe rat exposure test (RET) is a prey (mouse)-predator (rat) situation that activates brain defensive areas and elicits hormonal and defensive behavior in the mouse. Here, we investigated possible correlations between the spatiotemporal [time spent in protected (home chamber and tunnel) and unprotected (surface) compartments and frequency of entries into the three compartments] and ethological [e.g., duration of protected and unprotected stretched-attend postures (SAP), duration of contact with the rat's compartment] measures (Experiment 1). Secondly, we investigated the effects of systemic treatment with pro- or anti-aversive drugs on the behavior that emerged from the factor analysis (Experiment 2). The effects of chronic (21 days) imipramine and fluoxetine on defensive behavior were also investigated (Experiment 3). Exp. 1 revealed that the time in the protected compartment, protected SAP and rat contacts loaded on factor 1 (defensive behavior), while the total entries and unprotected SAP loaded on factor 2 (locomotor activity). Exp. 2 showed that alprazolam (but not diazepam) selectively changed the defensive factor. Caffeine produced a mild proaversive-like effect, whereas yohimbine only decreased locomotor activity (total entries). Fluoxetine (but not imipramine) produced a weak proaversive-like effect. 5-HT1A/5-HT2 receptor ligands did not change any behavioral measure. In Exp. 3, chronic fluoxetine (but not imipramine) attenuated the defensive behavior factor without changing locomotion. Given that the defensive factor was sensitive to drugs known to attenuate (alprazolam and chronic fluoxetine) and induce (caffeine) panic attack, we suggest the RET as a useful test to assess the effects of panicolytic and panicogenic drugs. © 2012 Elsevier B.V.en
dc.format.extent160-170-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectFactor analysis-
dc.subjectMice-
dc.subjectPanicogenic drugs-
dc.subjectPanicolytic drugs-
dc.subjectPrey-predator interaction-
dc.subjectRat exposure test-
dc.subjectalprazolam-
dc.subjectcaffeine-
dc.subjectdiazepam-
dc.subjectfluoxetine-
dc.subjectimipramine-
dc.subjectserotonin 1A receptor-
dc.subjectserotonin 2 receptor-
dc.subjectyohimbine-
dc.subjectacute drug administration-
dc.subjectanimal behavior-
dc.subjectanimal experiment-
dc.subjectattenuation-
dc.subjectaversive behavior-
dc.subjectbehavior change-
dc.subjectbody posture-
dc.subjectchronic drug administration-
dc.subjectclimbing-
dc.subjectcontrolled study-
dc.subjectdefensive behavior-
dc.subjectdose response-
dc.subjectdrug dose comparison-
dc.subjectdrug effect-
dc.subjectdrug potency-
dc.subjectexperimental test-
dc.subjectgrooming-
dc.subjectlocomotion-
dc.subjectlong term exposure-
dc.subjectmale-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectpanic-
dc.subjectpredator avoidance-
dc.subjectpredator prey interaction-
dc.subjectpriority journal-
dc.subjectrat-
dc.subjectrat exposure test-
dc.subjectvalidation process-
dc.subjectAdrenergic alpha-2 Receptor Antagonists-
dc.subjectAlprazolam-
dc.subjectAnimals-
dc.subjectAnti-Anxiety Agents-
dc.subjectAntidepressive Agents-
dc.subjectCaffeine-
dc.subjectCentral Nervous System Stimulants-
dc.subjectDiazepam-
dc.subjectEscape Reaction-
dc.subjectFactor Analysis, Statistical-
dc.subjectFluoxetine-
dc.subjectFood Chain-
dc.subjectImipramine-
dc.subjectMale-
dc.subjectMotor Activity-
dc.subjectPosture-
dc.subjectPredatory Behavior-
dc.subjectRats-
dc.subjectRats, Long-Evans-
dc.subjectTime Factors-
dc.subjectYohimbine-
dc.titleEthopharmacological evaluation of the rat exposure test: A prey-predator interaction testen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Goiás (UEG)-
dc.contributor.institutionFundación Universitaria Konrad Lorenz-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationLaboratory of Pharmacology School of Pharmaceutical Sciences Universidade Estadual Paulista, UNESP, Araraquara, SP 14801-902-
dc.description.affiliationJoint Graduate Program in Physiological Sciences UFSCar UNESP. Rod. Washington Luís, Km 235, São Carlos, SP 13565-905-
dc.description.affiliationUnidade Universitária de Ciências Exatas e Tecnológicas UnUCET-UEG, Br 153 n.3105, CEP: 75132-903 Anápolis, GO-
dc.description.affiliationLaboratory of Animal Behavior Fundación Universitaria Konrad Lorenz, Bogotá-
dc.description.affiliationInstitute for Neuroscience and Behavior-IneC USP, Ribeirão Preto, SP 14040-901-
dc.description.affiliationUnespLaboratory of Pharmacology School of Pharmaceutical Sciences Universidade Estadual Paulista, UNESP, Araraquara, SP 14801-902-
dc.description.affiliationUnespJoint Graduate Program in Physiological Sciences UFSCar UNESP. Rod. Washington Luís, Km 235, São Carlos, SP 13565-905-
dc.identifier.doi10.1016/j.bbr.2012.11.023-
dc.identifier.wosWOS:000319542600021-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofBehavioural Brain Research-
dc.identifier.scopus2-s2.0-84871387916-
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