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dc.contributor.authorJung, Yujung-
dc.contributor.authorCao, Yongkai-
dc.contributor.authorPaudel, Suresh-
dc.contributor.authorYoon, Goo-
dc.contributor.authorCheon, Seung Hoon-
dc.contributor.authorBae, Gyu-Un-
dc.contributor.authorJin, Li Tai-
dc.contributor.authorKim, Yong Kee-
dc.contributor.authorKim, Su-Nam-
dc.date.accessioned2024-01-20T01:33:55Z-
dc.date.available2024-01-20T01:33:55Z-
dc.date.created2021-09-01-
dc.date.issued2017-04-25-
dc.identifier.issn0009-2797-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/122834-
dc.description.abstractIn this study, we aimed to demonstrate the antidiabetic potential of (E)-N-(4-(3-(5-bromo-4-hydroxy-2-methoxyphenyl) acryloyl) phenyl)-4-tert-butylbenzamide (SN158) through peroxisome proliferator-activated receptor (PPAR)-alpha/gamma dual activation. SN158 interacted with both PPAR alpha and PPAR gamma, and increased their transcriptional activities. Simultaneously, SN158 treatment led to an increase in adipogenic differentiation of 3T3-L1 preadipocytes and fatty acid oxidation in hepatocytes. In addition, glucose uptake in myotubes was significantly increased by SN158 treatment. Finally, SN158 significantly lowered the plasma levels of glucose, triglycerides, and free fatty acids in ob/ob mice without severe weight gain and hepatomegaly. These results suggest that SN158 can be useful as a potential therapeutic agent against type 2 diabetes and related metabolic disorders by alleviating glucose and lipid abnormalities. (C) 2017 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.subjectAMERICAN-DIABETES-ASSOCIATION-
dc.subjectRECEPTOR-GAMMA-
dc.subjectEUROPEAN ASSOCIATION-
dc.subjectCONSENSUS STATEMENT-
dc.subjectLIPID-METABOLISM-
dc.subjectALPHA-
dc.subjectHYPERGLYCEMIA-
dc.subjectAGONISTS-
dc.subjectPHOSPHORYLATION-
dc.subjectAMORPHASTILBOL-
dc.titleAntidiabetic effect of SN158 through PPAR alpha/gamma dual activation in ob/ob mice-
dc.typeArticle-
dc.identifier.doi10.1016/j.cbi.2017.02.014-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCHEMICO-BIOLOGICAL INTERACTIONS, v.268, pp.24 - 30-
dc.citation.titleCHEMICO-BIOLOGICAL INTERACTIONS-
dc.citation.volume268-
dc.citation.startPage24-
dc.citation.endPage30-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000400460700003-
dc.identifier.scopusid2-s2.0-85014141435-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.type.docTypeArticle-
dc.subject.keywordPlusAMERICAN-DIABETES-ASSOCIATION-
dc.subject.keywordPlusRECEPTOR-GAMMA-
dc.subject.keywordPlusEUROPEAN ASSOCIATION-
dc.subject.keywordPlusCONSENSUS STATEMENT-
dc.subject.keywordPlusLIPID-METABOLISM-
dc.subject.keywordPlusALPHA-
dc.subject.keywordPlusHYPERGLYCEMIA-
dc.subject.keywordPlusAGONISTS-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusAMORPHASTILBOL-
dc.subject.keywordAuthor(E)-N-(4-(3-(5-bromo-4-hydroxy-2-methoxyphenyl)acryloyl)phenyl)-4-tert-b utylbenzamide-
dc.subject.keywordAuthorSN158-
dc.subject.keywordAuthorPPAR alpha/gamma agonist-
dc.subject.keywordAuthorInsulin sensitivity-
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