dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.contributorUniversidade de São Paulo (USP)
dc.creatorSilva, Mariana Santos Carvalho de Faria [UNIFESP]
dc.creatorPereira, Bruno Aranha [UNIFESP]
dc.creatorCéspedes, Isabel Cristina [UNIFESP]
dc.creatorNascimento, Juliana Olivetti Guzman [UNIFESP]
dc.creatorBittencourt, Jackson C.
dc.creatorViana, Milena de Barros [UNIFESP]
dc.date.accessioned2016-01-24T14:37:48Z
dc.date.accessioned2022-10-07T20:32:50Z
dc.date.available2016-01-24T14:37:48Z
dc.date.available2022-10-07T20:32:50Z
dc.date.created2016-01-24T14:37:48Z
dc.date.issued2014-09-01
dc.identifierBehavioural Brain Research. Amsterdam: Elsevier B.V., v. 271, p. 249-257, 2014.
dc.identifier0166-4328
dc.identifierhttps://repositorio.unifesp.br/handle/11600/38156
dc.identifier10.1016/j.bbr.2014.06.018
dc.identifierWOS:000340323000034
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4019287
dc.description.abstractCorticotropin-releasing factor (CRF) plays a critical role in the mediation of physiological and behavioral responses to stressors. in the present study, we investigated the role played by the CRF system within the dorsomedial hypothalamus (DMH) in the modulation of anxiety- and panic-related responses. Male Wistar rats were administered into the DMH with CRF (125 and 250 ng/0.2 mu l, experiment 1) or with the CRFR1 antagonist antalarmin (25 ng/0.2 mu l, experiment 2) and 10 min later tested in the elevated T-maze (ETM) for inhibitory avoidance and escape measurements. in clinical terms, these responses have been respectively related to generalized anxiety and panic disorder. To further verify if the anxiogenic effects of CRF were mediated by CRFR1 activation, we also investigated the effects of the combined treatment with CRF (250 ng/0.2 mu l) and antalarmin (25 ng/0.2 mu l) (experiment 3). All animals were tested in an open field, immediately after the ETM, for locomotor activity assessment. Results showed that 250 ng/0.2 mu l of CRF facilitated ETM avoidance, an anxiogenic response. Antalarmin significantly decreased avoidance latencies, an anxiolytic effect, and was able to counteract the anxiogenic effects of CRF. None of the compounds administered altered escape responses or locomotor activity measurements. These results suggest that CRF in the DMH exerts anxiogenic effects by activating type 1 receptors, which might be of relevance to the physiopathology of generalized anxiety disorder. (C) 2014 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationBehavioural Brain Research
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.rightsAcesso restrito
dc.subjectCorticotropin-releasing factor
dc.subjectCRF
dc.subjectDorsomedial hypothalamus
dc.subjectElevated T-maze
dc.subjectAnxiety
dc.subjectPanic
dc.titleDorsomedial hypothalamus CRF type 1 receptors selectively modulate inhibitory avoidance responses in the elevated T-maze
dc.typeArtigo


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