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Enhanced odor discrimination learning in aged Bax-KO mice

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dc.contributor.authorKim, Woon Ryoung-
dc.contributor.authorSun, Woong-
dc.date.accessioned2021-09-05T22:36:49Z-
dc.date.available2021-09-05T22:36:49Z-
dc.date.created2021-06-14-
dc.date.issued2013-08-26-
dc.identifier.issn0304-3940-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102424-
dc.description.abstractThroughout life, new neurons are continuously generated from subventricular zone and added to the olfactory bulb (OB). Because a subset of mature OB neurons undergoes spontaneous cell death, adult OB neurogenesis serves for the replacement of this cell loss. Spontaneous cell turnover should alter the neuronal circuits, but the significance of cell turnover on olfactory learning is yet poorly understood. In this study, we explored the olfactory learning behaviors of model mice showing (1) absence of cell death and cell addition (aged Bax-KO mice); (2) absence of cell death but presence of cell addition (young Bax-KO mice); or (3) presence cell death but absence of cell addition (surgical lesion of rostral migratory stream of neuroblasts). Interestingly, aged Bax-KO mice with no cell replacement acquired the ability to discriminate odor differences faster than WT littermates, whereas other model mice exhibited virtually normal learning ability. These results suggest that the cell replacement is necessary for the normal olfactory learning behavior, and the chronic perturbation of cell replacement may result in the imbalance of neural circuits driving unexpected enhancement of olfactory learning ability. (C) 2013 Elsevier Ireland Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectADULT OLFACTORY-BULB-
dc.subjectNEWLY GENERATED NEURONS-
dc.subjectPROGRAMMED CELL-DEATH-
dc.subjectNEWBORN NEURONS-
dc.subjectHIPPOCAMPAL NEUROGENESIS-
dc.subjectMAMMALIAN BRAIN-
dc.subjectTERM SURVIVAL-
dc.subjectMIGRATION-
dc.subjectAUTISM-
dc.subjectPLASTICITY-
dc.titleEnhanced odor discrimination learning in aged Bax-KO mice-
dc.typeArticle-
dc.contributor.affiliatedAuthorSun, Woong-
dc.identifier.doi10.1016/j.neulet.2013.05.017-
dc.identifier.scopusid2-s2.0-84880133224-
dc.identifier.wosid000322092000037-
dc.identifier.bibliographicCitationNEUROSCIENCE LETTERS, v.548, pp.196 - 200-
dc.relation.isPartOfNEUROSCIENCE LETTERS-
dc.citation.titleNEUROSCIENCE LETTERS-
dc.citation.volume548-
dc.citation.startPage196-
dc.citation.endPage200-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusADULT OLFACTORY-BULB-
dc.subject.keywordPlusNEWLY GENERATED NEURONS-
dc.subject.keywordPlusPROGRAMMED CELL-DEATH-
dc.subject.keywordPlusNEWBORN NEURONS-
dc.subject.keywordPlusHIPPOCAMPAL NEUROGENESIS-
dc.subject.keywordPlusMAMMALIAN BRAIN-
dc.subject.keywordPlusTERM SURVIVAL-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusAUTISM-
dc.subject.keywordPlusPLASTICITY-
dc.subject.keywordAuthorCell death-
dc.subject.keywordAuthorAdult neurogenesis-
dc.subject.keywordAuthorOlfactory bulb-
dc.subject.keywordAuthorOdor discrimination learning-
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