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Cited 51 time in webofscience Cited 14 time in scopus
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dc.contributor.authorLee, JS-
dc.contributor.authorPark, AH-
dc.contributor.authorLee, SH-
dc.contributor.authorLee, SH-
dc.contributor.authorKim, JH-
dc.contributor.authorYang, SJ-
dc.contributor.authorIl Yeom, Y-
dc.contributor.authorKwak, TH-
dc.contributor.authorLee, D-
dc.contributor.authorLee, SJ-
dc.contributor.authorLee, CH-
dc.contributor.authorKim, JM-
dc.contributor.authorKim, D-
dc.date.accessioned2015-06-25T03:24:21Z-
dc.date.available2015-06-25T03:24:21Z-
dc.date.created2016-02-15-
dc.date.issued2012-10-11-
dc.identifier.issn1932-6203-
dc.identifier.other2015-OAK-0000026256en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/12667-
dc.description.abstractNADH-quinone oxidoreductase 1 (NQO1) modulates cellular NAD(+)/NADH ratio which has been associated with the aging and anti-aging mechanisms of calorie restriction (CR). Here, we demonstrate that the facilitation of NQO1 activity by feeding beta-lapachone (beta L), an exogenous NQO1 co-substrate, prevented age-dependent decline of motor and cognitive function in aged mice. beta L-fed mice did not alter their food-intake or locomotor activity but did increase their energy expenditure as measured by oxygen consumption and heat generation. Mitochondrial structure and numbers were disorganized and decreased in the muscles of control diet group but those defects were less severe in beta L-fed aged mice. Furthermore, for a subset of genes associated with energy metabolism, mice fed the beta L-diet showed similar changes in gene expression to the CR group (fed 70% of the control diet). These results support the potentiation of NQO1 activity by a beta L diet and could be an option for preventing age-related decline of muscle and brain functions.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherPublic Library of Science-
dc.relation.isPartOfPLOS ONE-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleBeta-Lapachone, a Modulator of NAD Metabolism, Prevents Health Declines in Aged Mice-
dc.typeArticle-
dc.contributor.college정보전자융합공학부en_US
dc.identifier.doi10.1371/JOURNAL.PONE-
dc.author.googleLee, JSen_US
dc.author.googlePark, AHen_US
dc.author.googleKim, Den_US
dc.author.googleKim, JMen_US
dc.author.googleLee, CHen_US
dc.author.googleLee, SJen_US
dc.author.googleLee, Den_US
dc.author.googleKwak, THen_US
dc.author.googleIl Yeom, Yen_US
dc.author.googleYang, SJen_US
dc.author.googleKim, JHen_US
dc.author.googleLee, SHen_US
dc.relation.volume7en_US
dc.relation.issue10en_US
dc.contributor.id10201212en_US
dc.relation.journalPLOS ONEen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationPLOS ONE, v.7, no.10-
dc.identifier.wosid000309807700055-
dc.date.tcdate2019-01-01-
dc.citation.number10-
dc.citation.titlePLOS ONE-
dc.citation.volume7-
dc.contributor.affiliatedAuthorLee, SJ-
dc.identifier.scopusid2-s2.0-84992324005-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc24-
dc.description.scptc3*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusGENE-EXPRESSION PROFILE-
dc.subject.keywordPlusCALORIE RESTRICTION-
dc.subject.keywordPlusLIFE-SPAN-
dc.subject.keywordPlusSKELETAL-MUSCLE-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusCANCER-CELLS-
dc.subject.keywordPlusEXTENDS LIFE-
dc.subject.keywordPlusMITOCHONDRIAL-
dc.subject.keywordPlusYEAST-
dc.subject.keywordPlusANTIOXIDANT-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-

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이승재LEE, SEUNG JAE
Dept of Life Sciences
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