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Epicatechin elicits MyoD-dependent myoblast differentiation and myogenic conversion of fibroblasts

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dc.contributor.authorLee, Sang-Jin-
dc.contributor.authorLeem, Young-Eun-
dc.contributor.authorGo, Ga-Yeon-
dc.contributor.authorChoi, Younhee-
dc.contributor.authorSong, Yoo Jin-
dc.contributor.authorKim, Insol-
dc.contributor.authorKim, Do Yoon-
dc.contributor.authorKim, Yong Kee-
dc.contributor.authorSeo, Dong-Wan-
dc.contributor.authorKang, Jong-Sun-
dc.contributor.authorBae, Gyu-Un-
dc.date.available2021-02-22T11:15:22Z-
dc.date.issued2017-04-
dc.identifier.issn1932-6203-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/8588-
dc.description.abstractPrevention of age-associated reduction in muscle mass and function is required to manage a healthy life. Supplemental (-)-Epicatechin (EC) appears to act as a potential regulator for muscle growth and strength. However, its cellular and molecular mechanisms as a potential muscle growth agent have not been studied well. In the current study, we investigated a role of EC in differentiation of muscle progenitors to gain the molecular insight into how EC regulates muscle growth. EC enhanced myogenic differentiation in a dose-dependent manner through stimulation of promyogenic signaling pathways, p38MAPK and Akt. EC treatment elevated MyoD activity by enhancing its heterodimerization with E protein. Consistently, EC also positively regulated myogenic conversion and differentiation of fibroblasts. In conclusion, EC has a potential as a therapeutic or nutraceutical remedy to treat degenerative muscle diseases or age-related muscle weakness.-
dc.language영어-
dc.language.isoENG-
dc.publisherPUBLIC LIBRARY SCIENCE-
dc.titleEpicatechin elicits MyoD-dependent myoblast differentiation and myogenic conversion of fibroblasts-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1371/journal.pone.0175271-
dc.identifier.scopusid2-s2.0-85017146187-
dc.identifier.wosid000399371900144-
dc.identifier.bibliographicCitationPLOS ONE, v.12, no.4-
dc.citation.titlePLOS ONE-
dc.citation.volume12-
dc.citation.number4-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusSKELETAL-MUSCLE-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlus(-)-EPICATECHIN-
dc.subject.keywordPlusRESTRICTION-
dc.subject.keywordPlusSARCOPENIA-
dc.subject.keywordPlusPROMOTER-
dc.subject.keywordPlusTEA-
dc.identifier.urlhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0175271-
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