Frustrated expected reward induces differential transcriptional changes in the mouse brain

dc.contributor.authorMartín-García, E.
dc.contributor.authorFernàndez Castillo, Noèlia
dc.contributor.authorBurokas, A.
dc.contributor.authorGutiérrez-Cuesta, J.
dc.contributor.authorSánchez Mora, Cristina
dc.contributor.authorCasas, M.
dc.contributor.authorRibasés Haro, Marta
dc.contributor.authorCormand Rifà, Bru
dc.contributor.authorMaldonado, Rafael, 1961-
dc.date.accessioned2019-01-31T15:48:00Z
dc.date.available2019-01-31T15:48:00Z
dc.date.issued2015-01
dc.date.updated2019-01-31T15:48:00Z
dc.description.abstractFrustration represents a particular aspect of the addictive process that is related to loss of control when the expected reward is not obtained. We aim to study the consequences of frustrated expected reward on gene expression in the mouse brain. For this purpose, we used an operant model of frustration using palatable food as reward combined with microarrays. Transcriptomic profiles of frontal cortex, ventral striatum and hippocampus were analysed in five groups of mice: (1) positive control receiving palatable food and the cue light as conditioned stimulus; (2) frustrated group only receiving the cue light; (3) extinction learning group that did not receive palatable food nor the light; (4) negative control that never received the reinforcer nor the light during the whole experiment; and (5) yoked that received palatable food passively. Gene expression changes produced by frustration were revealed in the frontal cortex and ventral striatum, but not in the hippocampus. Most of the changes, such as the modification of the dopamine-DARPP-32 signalling pathway, were common in both areas and estimated to have neuronal origin. Extinction learning induced transcriptional changes only in the ventral striatum, with most genes showing down-regulation and without alteration in the dopamine-DARPP-32 signalling pathway. Active palatable food-seeking behaviour induced changes in gene expression in ventral striatum mainly affecting cell communication. In conclusion, frustration behaviour-induced changes in frontal cortex and ventral striatum mainly related to dopamine-DARPP-32 signalling that could play an important role in the loss of behavioural control during the addictive processes.
dc.format.extent16 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec643616
dc.identifier.issn1355-6215
dc.identifier.pmid25288320
dc.identifier.urihttps://hdl.handle.net/2445/127788
dc.language.isoeng
dc.publisherWiley
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1111/adb.12188
dc.relation.ispartofAddiction Biology, 2015, vol. 20, num. 1, p. 22-37
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/602805/EU//AGGRESSOTYPE
dc.relation.urihttps://doi.org/10.1111/adb.12188
dc.rights(c) Society for the Study of Addiction, 2015
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Genètica, Microbiologia i Estadística)
dc.subject.classificationExpressió gènica
dc.subject.classificationCervell
dc.subject.classificationFrustració
dc.subject.classificationRates (Animals de laboratori)
dc.subject.otherGene expression
dc.subject.otherBrain
dc.subject.otherFrustration
dc.subject.otherRats as laboratory animals
dc.titleFrustrated expected reward induces differential transcriptional changes in the mouse brain
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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