Anxiolytic-like effect of way-100635 microinfusions into the median (but not dorsal) raphe nucleus in mice exposed to the plus-maze: influence of prior test experience
dc.contributor.author | Canto-De-Souza, A. | |
dc.contributor.author | Nunes-De-Souza, R. L. | |
dc.contributor.author | Rodgers, R. J. | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Universidade Federal de São Carlos (UFSCar) | |
dc.contributor.institution | Univ Leeds | |
dc.date.accessioned | 2014-05-20T13:24:37Z | |
dc.date.available | 2014-05-20T13:24:37Z | |
dc.date.issued | 2002-02-22 | |
dc.description.abstract | Studies in several laboratories have confirmed the anxiolytic potential of a wide range of 5-HT1A receptor antagonists in rats and mice, with recent evidence pointing to a postsynaptic site of action in the ventral hippocampus. It would, therefore, be predicted that blockade of 5-HT1A somatodendritic autoreceptors in the midbrain raphe nuclei should produce anxiogenic-like effects. To test this hypothesis, we investigated the effects of WAY-100635 microinfusions (0, 1.0 or 3.0 mug in 0.1 mul) into the dorsal (DRN) or median (MRN) raphe nuclei on behaviours displayed by male Swiss-Webster mice in the elevated plus-maze. As this test is sensitive to prior experience. The effects of intra-raphe infusions were examined both in maze-naive and maze-experienced subjects. Sessions, were videotaped and subsequently scored for conventional indices of anxiety (open arm avoidance) and locomotor activity (closed arm entries), as well as a range of ethological measures (e.g. risk assessment). In maze-naive mice, intra-MRN (but not intra-DRN) infusions of WAY-100635 (3.0 mug) increased open arm exploration and reduced risk assessment. Importantly, these effects could not be attributed to a general reduction in locomotor activity. A similar, though somewhat weaker, pattern of behavioural change was observed in maze-experienced animals. This unexpected anxiolytic effect of 5-HT1A autoreceptor blockade in the MRN cannot be accounted fur by a disinhibition of 5-HT release in forebrain targets (e.g. hippocampus and amygdala), where stimulation of postsynaptic 5-HT1A receptors enhances anxiety-like responses. However, as the MRN also projects to the periaqueductal gray matter (PAG), an area known to be sensitive to the anti-aversive effects or 5-HT, it is argued that present results may reflect increased 5-HT release at this crucial midbrain locus within the neural circuitry of defense. (C) 2002 Elsevier B.V. B.V. All rights reserved. | en |
dc.description.affiliation | UNESP, Fac Ciências Farmaceut, Farmacol Lab, BR-14801902 Araraquara, SP, Brazil | |
dc.description.affiliation | Univ Fed Sao Carlos, Dept Psicol, BR-13560 Sao Carlos, SP, Brazil | |
dc.description.affiliation | Univ Leeds, Dept Psychol, Lab Behab Pharmacol, Leeds LS2 9JT, W Yorkshire, England | |
dc.description.affiliationUnesp | UNESP, Fac Ciências Farmaceut, Farmacol Lab, BR-14801902 Araraquara, SP, Brazil | |
dc.format.extent | 50-59 | |
dc.identifier | http://dx.doi.org/10.1016/S0006-8993(01)03354-6 | |
dc.identifier.citation | Brain Research. Amsterdam: Elsevier B.V., v. 928, n. 1-2, p. 50-59, 2002. | |
dc.identifier.doi | 10.1016/S0006-8993(01)03354-6 | |
dc.identifier.issn | 0006-8993 | |
dc.identifier.uri | http://hdl.handle.net/11449/7700 | |
dc.identifier.wos | WOS:000174374800006 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Brain Research | |
dc.relation.ispartofjcr | 3.125 | |
dc.relation.ispartofsjr | 1,404 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Web of Science | |
dc.subject | 5-HT1A receptor | pt |
dc.subject | anxiety | pt |
dc.subject | median raphe nucleus | pt |
dc.subject | dorsal raphe nucleus | pt |
dc.subject | elevated plus-maze | pt |
dc.subject | WAY-100635 | pt |
dc.subject | mice | pt |
dc.title | Anxiolytic-like effect of way-100635 microinfusions into the median (but not dorsal) raphe nucleus in mice exposed to the plus-maze: influence of prior test experience | en |
dc.type | Artigo | |
dcterms.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dcterms.rightsHolder | Elsevier B.V. |
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