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Curcumin Stimulates Glucose Uptake Through AMPK-p38 MAPK Pathways in L6 Myotube Cells

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dc.contributor.authorKim, Ji Hae-
dc.contributor.authorPark, Ji Man-
dc.contributor.authorKim, Eung-Kyun-
dc.contributor.authorLee, Jung Ok-
dc.contributor.authorLee, Soo Kyung-
dc.contributor.authorJung, Jin Hee-
dc.contributor.authorYou, Ga Young-
dc.contributor.authorPark, Sun Hwa-
dc.contributor.authorSuh, Pann-Ghill-
dc.contributor.authorKim, Hyeon Soo-
dc.date.accessioned2021-09-08T02:40:46Z-
dc.date.available2021-09-08T02:40:46Z-
dc.date.created2021-06-11-
dc.date.issued2010-06-
dc.identifier.issn0021-9541-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/116316-
dc.description.abstractCurcumin has been shown to exert a variety of beneficial human health effects. However, mechanisms by which curcumin acts are poorly understood. In this study, we report that curcumin activated AMP-activated protein kinase (AMPK) and increased glucose uptake in rat L6 myotubes. In addition, curcumin activated the mitogen-activated protein kinase kinase (MEK)3/6-p38 mitogen-activated protein kinase (MAPK) signaling pathways in the downstream of the AMPK cascade. Moreover, inhibition of either AMPK or p38 MAPK resulted in blockage of curcumin-induced glucose uptake. Furthermore, the administration of curcumin to mice increased AMPK phosphorylation in the skeletal muscles. Taken together, these results indicate that the beneficial health effect of curcumin can be explained by its ability to activate AMPK-p38 MAPK pathways in skeletal muscles. J. Cell. Physiol. 223: 771-778, 2010. (C) 2010 Wiley-Liss, Inc.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectACTIVATED PROTEIN-KINASE-
dc.subjectSKELETAL-MUSCLE-
dc.subjectGLUT4 TRANSLOCATION-
dc.subjectANTIINFLAMMATORY AGENT-
dc.subjectLIPID-PEROXIDATION-
dc.subject3T3-L1 ADIPOCYTES-
dc.subjectRAT-LIVER-
dc.subjectTRANSPORT-
dc.subjectINSULIN-
dc.subjectALPHA-
dc.titleCurcumin Stimulates Glucose Uptake Through AMPK-p38 MAPK Pathways in L6 Myotube Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Sun Hwa-
dc.contributor.affiliatedAuthorKim, Hyeon Soo-
dc.identifier.doi10.1002/jcp.22093-
dc.identifier.scopusid2-s2.0-77951244999-
dc.identifier.wosid000277482900026-
dc.identifier.bibliographicCitationJOURNAL OF CELLULAR PHYSIOLOGY, v.223, no.3, pp.771 - 778-
dc.relation.isPartOfJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.titleJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.volume223-
dc.citation.number3-
dc.citation.startPage771-
dc.citation.endPage778-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusACTIVATED PROTEIN-KINASE-
dc.subject.keywordPlusSKELETAL-MUSCLE-
dc.subject.keywordPlusGLUT4 TRANSLOCATION-
dc.subject.keywordPlusANTIINFLAMMATORY AGENT-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlus3T3-L1 ADIPOCYTES-
dc.subject.keywordPlusRAT-LIVER-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusINSULIN-
dc.subject.keywordPlusALPHA-
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