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dc.contributor.authorCastro, Elena-
dc.contributor.authorAmigó, Josep-
dc.contributor.authorVidal, Rebeca-
dc.contributor.authorPilar-Cuéllar, Fuencisla-
dc.contributor.authorMartín, Alicia-
dc.contributor.authorValdizán, Elsa M.-
dc.contributor.authorPazos, Ángel-
dc.contributor.authorDíaz, Álvaro-
dc.date.accessioned2016-03-31T10:49:20Z-
dc.date.available2016-03-31T10:49:20Z-
dc.date.issued2014-
dc.identifier.citation9th FENS Forum (2014)-
dc.identifier.urihttp://hdl.handle.net/10261/130662-
dc.descriptionResumen del póster presentado al 9th FENS: Forum of Neuroscience, celebrado en Milan (Italia) del 5 al 9 de julio de 2014.-
dc.description.abstractNew pharmacological strategiesfor treating depression include 5-HT4 receptor agonists since theyare reported to have a faster onset of antidepressant actions versusconventional antidepressants. We have evaluated the anxiolytic profile of the5-HT4 receptor agonist RS67,333 (1.5, 3 and 6 mg/kg/day, i.p.) in C57/BL6mice after acute (30 min) and subchronic administration (3 days). Acute RS67,333induced a dose-dependent anxiolytic effect as evidenced by an increased centralactivity in the open field test: a) entries=23±4.5 (p<0.01); 31±4.3 (p<0.001) and 32±2.9 (p<0.001) for 1.5, 3 and 6 mg/kgof RS67,333 respectively vs 10±1.6for vehicle group, b) distance=3.0±0.4 (p<0.01); 4.3±0.6 (p<0.001) and 3.9±0.6 (p<0.001) for 1.5, 3 and 6 mg/kg of RS67,333 vs 1.1±0.2 for vehicle group, and c)time (s)= 25.8±4.6; 44.6±9.6 (p<0.05)and 57.0±9.0 (p<0.01) for 1.5, 3 and 6 mg/kg of RS67333 vs 20.8±3.0 for vehicle group. Interestingly, the anxiolyticprofile of RS67,333 is also observed 24 hours after 3-day subchronic administrationas evidenced by a significant reductionin the latency to feed in the novelty suppressed feeding (NSF), reaching themaximal effect with the dose of 6 mg/kg/day (% reduction= 59.9±3.1, p<0.05).Moreover, a clear dose-dependent anxiolytic effect of RS67,333 in the NSF was alsopresent following its administration for 7 days. In conclusion, our study demonstratenot only the immediate anxiolytic effect of RS67,333 but also its rapid onsetof action in the behavioural paradigm (NSF), a predictive test ofantidepressants.-
dc.description.sponsorshipSupported by: Ministerio de Ciencia (SAF07-61862) y Ministerio de Economía y Competitividad (SAF2011-25020).-
dc.rightsclosedAccess-
dc.titleAnxiolytic-like effect after acute and subchronic administration of the selective 5-HT4 receptor partial agonist RS67,333-
dc.typepóster de congreso-
dc.date.updated2016-03-31T10:49:20Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
Appears in Collections:(IBBTEC) Comunicaciones congresos
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