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Maternal separation stress in male mice: long-term increases in alcohol intake

dc.contributor.authorCruz, Fabio C. [UNESP]
dc.contributor.authorQuadros, Isabel M.
dc.contributor.authorPlaneta, Cleopatra da Silva [UNESP]
dc.contributor.authorMiczek, Klaus A.
dc.contributor.institutionTufts Univ
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:25:34Z
dc.date.available2014-05-20T13:25:34Z
dc.date.issued2008-12-01
dc.description.abstractIn rodents, prolonged maternal separation has been used as a model of developmentally early environmental stress to influence adult drug intake.The aim of the present study was to evaluate the long-term effects of prolonged maternal separation on alcohol consumption using two different self-administration procedures in mice: operant alcohol self-administration vs. three-bottle choice.From postnatal day (PND) 1 to 14, pups were separated from the dam (maternal separation, MS) daily for 180 min or were left undisturbed, only handled during cage cleaning (animal facility rearing, AFR). on PND 60, they were assigned to one of two experimental manipulations: either a three-bottle choice or operant oral alcohol self-administration. In the three-bottle choice procedure, mice were given access to 6% or 10% alcohol or 0.05% saccharin solution for 2 h/day for 10 days. In the second experiment, mice were reinforced for nose poking by delivery of oral alcohol (6% or 10% in saccharin) or 0.05% saccharin solutions during daily 30-min sessions. Following the acquisition phase, break points were determined. Later, mice were allowed 1 h access to the reinforcing solution with no dosage limitation.In the three-bottle choice procedure, MS mice showed higher alcohol intake than AFR at the 10% alcohol concentration. In the operant alcohol self-administration, MS mice achieved higher alcohol intake than AFR at the concentrations 6% and 10% during the 1-h session.The results demonstrate the long-term consequences of MS on alcohol intake in male mice, suggesting early life stress as a risk factor for alcohol consumption and abuse.en
dc.description.affiliationTufts Univ, Dept Psychol, Medford, MA 02155 USA
dc.description.affiliationTufts Univ, Dept Psychiat, Medford, MA 02155 USA
dc.description.affiliationTufts Univ, Dept Pharmacol & Expt Therapeut, Medford, MA 02155 USA
dc.description.affiliationTufts Univ, Dept Neurosci, Medford, MA 02155 USA
dc.description.affiliationUniversidade Federal de São Carlos (UFSCar), Grad Program Physiol Sci, BR-13560 São Carlos, SP, Brazil
dc.description.affiliationSão Paulo State Univ, UNESP, Sch Pharmaceut Sci, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, UNESP, Sch Pharmaceut Sci, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipNIAAA
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdNIAAA: LambdaLambda0013983
dc.format.extent459-468
dc.identifierhttp://dx.doi.org/10.1007/s00213-008-1307-4
dc.identifier.citationPsychopharmacology. New York: Springer, v. 201, n. 3, p. 459-468, 2008.
dc.identifier.doi10.1007/s00213-008-1307-4
dc.identifier.issn0033-3158
dc.identifier.lattes2514762545280942
dc.identifier.orcid0000-0002-1378-6327
dc.identifier.urihttp://hdl.handle.net/11449/8117
dc.identifier.wosWOS:000261037300014
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofPsychopharmacology
dc.relation.ispartofjcr3.222
dc.relation.ispartofsjr1,494
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectMaternal separationen
dc.subjectAlcoholen
dc.subjectEthanolen
dc.subjectMiceen
dc.subjectOperant conditioningen
dc.subjectThree-bottle choiceen
dc.subjectSelf-administrationen
dc.titleMaternal separation stress in male mice: long-term increases in alcohol intakeen
dc.typeArtigopt
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes2514762545280942[3]
unesp.author.orcid0000-0002-1378-6327[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt

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