Afficher la notice abrégée

dc.rights.licenseopenen_US
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorVAN WAES, Vincent
hal.structure.identifierNutrition et Neurobiologie intégrée [NutriNeuro]
dc.contributor.authorDARNAUDERY, Muriel
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorMARROCCO, Jordan
hal.structure.identifierKarolinska Institutet [Stockholm]
dc.contributor.authorGRUBER, Samuel H.
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorTALAVERA, Enrique
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorMAIRESSE, Jerome
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorVAN CAMP, Gilles
dc.contributor.authorCASOLLA, Barbara
hal.structure.identifierIstituto Neurologico Mediterraneo [NEUROMED I.R.C.C.S.]
dc.contributor.authorNICOLETTI, Ferdinando
hal.structure.identifierKarolinska Institutet [Stockholm]
dc.contributor.authorMATHE, Aleksander A.
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorMACCARI, Stephania
hal.structure.identifierUnité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
dc.contributor.authorMORLEY-FLETCHER, Sara
dc.date.accessioned2022-03-02T13:55:13Z
dc.date.available2022-03-02T13:55:13Z
dc.date.issued2011-08-01
dc.identifier.issn1872-7549en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/128795
dc.description.abstractEnWe examined the interaction between early life stress and vulnerability to alcohol in female rats exposed to prenatal restraint stress (PRS rats). First we studied the impact of PRS on ethanol preference during adolescence. PRS slightly increased ethanol preference per se, but abolished the effect of social isolation on ethanol preference. We then studied the impact of PRS on short- and long-term responses to ethanol focusing on behavioral and neurochemical parameters related to depression/anxiety. PRS or unstressed adolescent female rats received 10% ethanol in the drinking water for 4 weeks from PND30 to PND60. At PND60, the immobility time in the forced-swim test did not differ between PRS and unstressed rats receiving water alone. Ethanol consumption had no effect in unstressed rats, but significantly reduced the immobility time in PRS rats. In contrast, a marked increase in the immobility time was seen after 5 weeks of ethanol withdrawal only in unstressed rats. Hippocampal levels of neuropeptide Y (NPY) and mGlu1a metabotropic glutamate receptors were increased at the end of ethanol treatment only in unstressed rats. Ethanol treatment had no effect on levels of corticotropin-releasing hormone (CRH) in the hippocampus, striatum, and prefrontal cortex of both groups of rats. After ethanol withdrawal, hippocampal levels of mGlu1 receptors were higher in unstressed rats, but lower in PRS rats, whereas NPY and CRH levels were similar in the two groups of rats. These data indicate that early life stress has a strong impact on the vulnerability and responsiveness to ethanol consumption during adolescence.
dc.language.isoENen_US
dc.subject.enAlcohol Drinking
dc.subject.enAnimals
dc.subject.enChoice Behavior
dc.subject.enCorpus Striatum
dc.subject.enCorticotropin-Releasing Hormone
dc.subject.enEthanol
dc.subject.enFemale
dc.subject.enHippocampus
dc.subject.enImmobility Response
dc.subject.enTonic
dc.subject.enMale
dc.subject.enNeuropeptide Y
dc.subject.enPrefrontal Cortex
dc.subject.enPregnancy
dc.subject.enPrenatal Exposure Delayed Effects
dc.subject.enRats
dc.subject.enRats
dc.subject.enSprague-Dawley
dc.subject.enReceptors
dc.subject.enMetabotropic Glutamate
dc.subject.enSocial Isolation
dc.subject.enStress
dc.subject.enPhysiological
dc.title.enImpact of early life stress on alcohol consumption and on the short- and long-term responses to alcohol in adolescent female rats.
dc.title.alternativeBehav Brain Resen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.bbr.2011.02.033en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed21376087en_US
bordeaux.journalBehavioural Brain Researchen_US
bordeaux.page43-49en_US
bordeaux.volume221en_US
bordeaux.hal.laboratoriesNutriNeurO (Laboratoire de Nutrition et Neurobiologie Intégrée) - UMR 1286en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Behavioural%20Brain%20Research&rft.date=2011-08-01&rft.volume=221&rft.issue=1&rft.spage=43-49&rft.epage=43-49&rft.eissn=1872-7549&rft.issn=1872-7549&rft.au=VAN%20WAES,%20Vincent&DARNAUDERY,%20Muriel&MARROCCO,%20Jordan&GRUBER,%20Samuel%20H.&TALAVERA,%20Enrique&rft.genre=article


Fichier(s) constituant ce document

FichiersTailleFormatVue

Il n'y a pas de fichiers associés à ce document.

Ce document figure dans la(les) collection(s) suivante(s)

Afficher la notice abrégée