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Identification of bioactive heterocyclic compounds from mulberry and their protective effect against streptozotocin-induced apoptosis in INS-1 cells

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dc.contributor.authorSong, Ji Hoon-
dc.contributor.authorLee, Dahae-
dc.contributor.authorLee, Seoung Rak-
dc.contributor.authorYu, Jae Sik-
dc.contributor.authorJang, Tae Su-
dc.contributor.authorNam, Joo-Won-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorKang, Ki Sung-
dc.date.available2020-02-27T11:41:22Z-
dc.date.created2020-02-07-
dc.date.issued2018-04-
dc.identifier.issn1791-2997-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3924-
dc.description.abstractA phytochemical investigation of the MeOH extracts from mulberries (the fruit of Morus alba L.) led to the identification of six heterocyclic compounds (1-6). These compounds were screened to detect whether they protected pancreatic INS-1 cells from streptozotocin (STZ)-induced cytotoxicity. Compound 3 was the most effective at preventing STZ-induced cytotoxicity and the production of reactive oxygen species (ROS) in INS-1 cells. In addition, compound 3 effectively prevented apoptosis induced by STZ in INS-1 cells. Compound 3 also prevented STZ-mediated cleavage of caspase-8, caspase-3 and poly (ADP-ribose) polymerase and increased the expression of B-cell lymphoma-2 (Bcl-2), an anti-apoptotic Bcl-2 family protein. In conclusion, the results of the present study indicate that compound 3 extracted from the fruit of M. alba was highly effective in preventing type 1 diabetes mellitus and may be a novel treatment option.-
dc.language영어-
dc.language.isoen-
dc.publisherSPANDIDOS PUBL LTD-
dc.relation.isPartOfMOLECULAR MEDICINE REPORTS-
dc.subjectTYPE-2 DIABETES-MELLITUS-
dc.subjectMORUS-ALBA L.-
dc.subjectHIGH-FAT-DIET-
dc.subjectOXIDATIVE STRESS-
dc.subjectBLOOD-GLUCOSE-
dc.subjectFRUIT-
dc.subjectRATS-
dc.subjectPOLYSACCHARIDES-
dc.subjectFLAVONOIDS-
dc.subjectDISEASE-
dc.titleIdentification of bioactive heterocyclic compounds from mulberry and their protective effect against streptozotocin-induced apoptosis in INS-1 cells-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000428672100142-
dc.identifier.doi10.3892/mmr.2018.8582-
dc.identifier.bibliographicCitationMOLECULAR MEDICINE REPORTS, v.17, no.4, pp.5982 - 5987-
dc.identifier.scopusid2-s2.0-85043291634-
dc.citation.endPage5987-
dc.citation.startPage5982-
dc.citation.titleMOLECULAR MEDICINE REPORTS-
dc.citation.volume17-
dc.citation.number4-
dc.contributor.affiliatedAuthorLee, Dahae-
dc.contributor.affiliatedAuthorKang, Ki Sung-
dc.type.docTypeArticle-
dc.subject.keywordAuthorMorus alba-
dc.subject.keywordAuthorstreptozotocin-
dc.subject.keywordAuthortype 1 diabetes mellitus-
dc.subject.keywordAuthorreactive oxygen species-
dc.subject.keywordPlusTYPE-2 DIABETES-MELLITUS-
dc.subject.keywordPlusMORUS-ALBA L.-
dc.subject.keywordPlusHIGH-FAT-DIET-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusBLOOD-GLUCOSE-
dc.subject.keywordPlusFRUIT-
dc.subject.keywordPlusRATS-
dc.subject.keywordPlusPOLYSACCHARIDES-
dc.subject.keywordPlusFLAVONOIDS-
dc.subject.keywordPlusDISEASE-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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