Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/132107
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dc.contributor.authorGenders, S.G.-
dc.contributor.authorScheller, K.J.-
dc.contributor.authorJaehne, E.J.-
dc.contributor.authorTurner, B.J.-
dc.contributor.authorLawrence, A.J.-
dc.contributor.authorBrunner, S.M.-
dc.contributor.authorKofler, B.-
dc.contributor.authorvan den Buuse, M.-
dc.contributor.authorDjouma, E.-
dc.date.issued2019-
dc.identifier.citationAddiction Biology, 2019; 24(5):886-897-
dc.identifier.issn1355-6215-
dc.identifier.issn1369-1600-
dc.identifier.urihttps://hdl.handle.net/2440/132107-
dc.description.abstractGalanin is a neuropeptide which mediates its effects via three G-protein coupled receptors (GAL₃ ). Administration of a GAL₃ antagonist reduces alcohol self-administration in animal models while allelic variation in the GAL₃ gene has been associated with an increased risk of alcohol use disorders in diverse human populations. Based on the association of GAL₃ with alcoholism, we sought to characterize drug-seeking behavior in GAL₃ -deficient mice for the first time. In the two-bottle free choice paradigm, GAL₃ -KO mice consistently showed a significantly increased preference for ethanol over water when compared to wildtype littermates. Furthermore, male GAL₃ -KO mice displayed significantly increased responding for ethanol under operant conditions. These differences in alcohol seeking behavior in GAL₃ -KO mice did not result from altered ethanol metabolism. In contrast to ethanol, GAL₃ -KO mice exhibited similar preference for saccharin and sucrose over water, and a similar preference for a high fat diet over a low fat diet as wildtype littermates. No differences in cognitive and locomotor behaviors were observed in GAL₃ -KO mice to account for increased alcohol seeking behavior. Overall, these findings suggest genetic ablation of GAL₃ in mice increases alcohol consumption.-
dc.description.statementofresponsibilityShannyn G. Genders, Karlene J. Scheller, Emily J. Jaehne, Bradley J. Turner, Andrew J. Lawrence, Susanne M. Brunner ... et al.-
dc.language.isoen-
dc.publisherWiley-
dc.rights© 2018 Society for the Study of Addiction-
dc.source.urihttp://dx.doi.org/10.1111/adb.12641-
dc.subjectAddiction; alcohol; galanin; galanin receptor-3-
dc.subject.meshAnimals-
dc.subject.meshMice, Knockout-
dc.subject.meshHyperkinesis-
dc.subject.meshEthanol-
dc.subject.meshMethamphetamine-
dc.subject.meshApomorphine-
dc.subject.meshDizocilpine Maleate-
dc.subject.meshReceptor, Galanin, Type 3-
dc.subject.meshDopamine Agonists-
dc.subject.meshExcitatory Amino Acid Antagonists-
dc.subject.meshCentral Nervous System Depressants-
dc.subject.meshCentral Nervous System Stimulants-
dc.subject.meshSelf Administration-
dc.subject.meshAlcohol Drinking-
dc.subject.meshMotor Activity-
dc.subject.meshEmotions-
dc.subject.meshFear-
dc.subject.meshInterpersonal Relations-
dc.subject.meshConditioning, Operant-
dc.subject.meshMaze Learning-
dc.subject.meshChoice Behavior-
dc.subject.meshPhenotype-
dc.subject.meshFemale-
dc.subject.meshMale-
dc.subject.meshSensory Gating-
dc.subject.meshDrug-Seeking Behavior-
dc.subject.meshReflex, Startle-
dc.subject.meshSpatial Memory-
dc.titleGAL₃ receptor knockout mice exhibit an alcohol-preferring phenotype-
dc.title.alternativeGAL(3) receptor knockout mice exhibit an alcohol-preferring phenotype-
dc.typeJournal article-
dc.identifier.doi10.1111/adb.12641-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1137024-
pubs.publication-statusPublished-
dc.identifier.orcidJaehne, E.J. [0000-0003-0532-1623]-
Appears in Collections:Biochemistry publications

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