Mostrar el registro sencillo

dc.contributor.authorPilar Cuéllar, María Fuencisla 
dc.contributor.authorVidal, Rebeca
dc.contributor.authorDíaz Martínez, Álvaro 
dc.contributor.authorGarro Martínez, Emilio
dc.contributor.authorLinge Méndez, Raquel
dc.contributor.authorCastro Fernández, María Elena 
dc.contributor.authorHaberzettl, Robert
dc.contributor.authorFink, Heidrun
dc.contributor.authorBert, Bettina
dc.contributor.authorBrosda, Jan
dc.contributor.authorRomero Presno, Beatriz
dc.contributor.authorCrespo Facorro, Benedicto 
dc.contributor.authorPazos Carro, Ángel 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2018-05-10T12:47:24Z
dc.date.available2018-11-15T03:45:11Z
dc.date.issued2017-11-15
dc.identifier.issn1948-7193
dc.identifier.otherSAF2011-25020es_ES
dc.identifier.otherSAF2015-67457-Res_ES
dc.identifier.urihttp://hdl.handle.net/10902/13675
dc.description.abstractPostsynaptic 5-HT1A receptors (5-HT1AR) play an important role in anxiety and stress, although their contribution is still controversial. Previous studies report that mice overexpressing postsynaptic 5-HT1ARs show no changes in basal anxiety, though the influence of stress conditions has not been addressed yet. In this study, we used this animal model to evaluate the role of 5-HT1ARs in anxiety response after pre-exposure to an acute stressor. Under basal conditions, 5-HT1AR overexpressing animals presented high corticosterone levels and a lower mineralocorticoid/ glucocorticoid receptor ratio. After pre-exposure to a single stressor, they showed a high anxiety-like response, associated with a blunted increase in corticosterone levels and higher c-Fos activation in the prefrontal cortex. Moreover, these mice also presented a lack of downregulation of hippocampal long-term potentiation after stress exposure. Therefore, higher postsynaptic 5-HT1AR activation might predispose to a high anxious phenotype and an impaired stress coping behavior.es_ES
dc.description.sponsorshipFunding sources: This research was supported by Spanish Ministry of Economy and Competitiveness (SAF2011-25020 and SAF2015-67457-R), Instituto de Salud Carlos III (FIS Grant PI13-00038) co-funded by the European Regional Development Fund (‘A way to buildEurope’) and Centro de Investigacion Biomedica en Red de Salud Mental(CIBERSAM).es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rights© ACS. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS chemical neuroscience, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://dx.doi.org/10.1021/acschemneuro.7b00156es_ES
dc.sourceACS Chem Neurosci. 2017 Nov 15;8(11):2393-2401es_ES
dc.subject.otherHPA axises_ES
dc.subject.otherPostsynaptic 5-HT1A receptores_ES
dc.subject.otheranxietyes_ES
dc.subject.otherbehaviores_ES
dc.subject.otherc-Foses_ES
dc.subject.otherlong-term potentiationes_ES
dc.titleEnhanced Stress Response in 5-HT1AR Overexpressing Mice: Altered HPA Function and Hippocampal Long-Term Potentiationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://dx.doi.org/10.1021/acschemneuro.7b00156es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1021/acschemneuro.7b00156
dc.type.versionacceptedVersiones_ES


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo