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Cited 3 time in webofscience Cited 5 time in scopus
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HD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies

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dc.contributor.authorKim, SoRa-
dc.contributor.authorKim, Dae Hoon-
dc.contributor.authorKim, Young-Seok-
dc.contributor.authorHa, Tae-Young-
dc.contributor.authorYang, Jin-
dc.contributor.authorPark, Soo Hyun-
dc.contributor.authorJeong, Kwang Won-
dc.contributor.authorRhee, Jae-Keol-
dc.date.available2020-02-28T16:42:44Z-
dc.date.created2020-02-06-
dc.date.issued2014-09-30-
dc.identifier.issn1976-9148-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12276-
dc.description.abstractG-protein coupled receptor 119 (GPR119) has emerged as a novel target for the treatment of type 2 diabetes mellitus. GPR119 is involved in glucose-stimulated insulin secretion (GSIS) from the pancreatic beta-cells and intestinal cells. In this study, we identified a novel small-molecule GPR119 agonist, HD047703, which raises intracellular cAMP concentrations in pancreatic beta-cells and can be expected to potentiate glucose-stimulated insulin secretion from human GPR119 receptor stably expressing cells (CHO cells). We evaluated the acute efficacy of HD047703 by the oral glucose tolerance test (OGTT) in normal C57BL/6J mice. Then, chronic administrations of HD047703 were performed to determine its efficacy in various diabetic rodent models. Single administration of HD047703 caused improved glycemic control during OGTT in a dose-dependent manner in normal mice, and the plasma GLP-1 level was also increased. With respect to chronic efficacy, we observed a decline in blood glucose levels in db/db, ob/ob and DIO mice. These results suggest that HD047703 may be a potentially promising anti-diabetic agent.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.relation.isPartOfBIOMOLECULES & THERAPEUTICS-
dc.subjectTYPE-2 DIABETES-MELLITUS-
dc.subjectINCRETIN-BASED THERAPIES-
dc.subjectGPR119 AGONISTS-
dc.subjectBODY-WEIGHT-
dc.subjectAGENTS-
dc.subjectNIDDM-
dc.subjectMOUSE-
dc.titleHD047703, a New Promising Anti-Diabetic Drug Candidate: In Vivo Preclinical Studies-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000342856200004-
dc.identifier.doi10.4062/biomolther.2014.035-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.22, no.5, pp.400 - 405-
dc.identifier.kciidART001915268-
dc.identifier.scopusid2-s2.0-84908042479-
dc.citation.endPage405-
dc.citation.startPage400-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume22-
dc.citation.number5-
dc.contributor.affiliatedAuthorJeong, Kwang Won-
dc.type.docTypeArticle-
dc.subject.keywordAuthorGPR119 agonist-
dc.subject.keywordAuthorType 2 diabetes-
dc.subject.keywordAuthorGLP-1-
dc.subject.keywordPlusTYPE-2 DIABETES-MELLITUS-
dc.subject.keywordPlusINCRETIN-BASED THERAPIES-
dc.subject.keywordPlusGPR119 AGONISTS-
dc.subject.keywordPlusBODY-WEIGHT-
dc.subject.keywordPlusAGENTS-
dc.subject.keywordPlusNIDDM-
dc.subject.keywordPlusMOUSE-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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