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DA-6034, a derivative of flavonoid, prevents and ameliorates dextran sulfate sodium-induced colitis and inhibits colon carcinogenesis

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dc.contributor.authorNam, Su Youn-
dc.contributor.authorKim, Joo Sung-
dc.contributor.authorKim, Jung Mogg-
dc.contributor.authorLee, Jong Yeul-
dc.contributor.authorKim, Nayoung-
dc.contributor.authorJung, Hyun Chae-
dc.contributor.authorSong, In Sung-
dc.date.accessioned2022-10-07T10:39:35Z-
dc.date.available2022-10-07T10:39:35Z-
dc.date.issued2008-02-
dc.identifier.issn1535-3702-
dc.identifier.issn1535-3699-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/172138-
dc.description.abstractPreviously, we have shown that DA-6034, a synthetic derivative of flavonoid eupatilin, inhibited NF-kappa B activation in colon epithelial cells and prevented trinitrobenzene sulfonic acid-induced rat colitis. The aim of this study was to investigate the preventive and therapeutic effect of DA-6034 on dextran sulfate sodium (DSS) - induced colitis and on inflammation-related cancer. C57BL/6 mice were given 4% DSS for 5 days with and without DA-6034 in the acute preventive model. In the acute therapeutic model, mice were given 4% DSS for 5 days followed by rectal administration of DA-6034. Colitis was quantified by body weight, disease activity index (DAI), colon length, and histology. In the inflammation-related cancer model, mice were given a single intraperitoneal injection of azoxymethane, then three cycles of 2% DSS for 5 days, then 2 weeks of free water consumption. Apoptosis was determined by in situ terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling assay, and the expression of Ki-67, phospho-kappa B kinase alpha (IKK alpha), and COX-2 were evaluated by immunohistochemistry. In both the acute preventive and acute therapeutic models, DA-6034 significantly attenuated DSS-induced weight loss, an increase in DAI, and a shortening of colon length. DA-6034 - treated mice maintained crypt architecture and revealed a scanty infiltration of inflammatory cells in both the preventive and therapeutic models. In the inflammation-related cancer model, DA-6034 reduced the number of colon tumors and ameliorated weight loss and shortening of colon length. DA-6034 strongly enhanced apoptosis and inhibited the expression of COX-2 and phospho-IKK alpha in inflammation-related colon cancer models. Our results suggest that DA-6034 prevents acute murine colitis and inhibits inflammation-related colon carcinogenesis. DA-6034 could be a potential therapeutic agent for inflammatory bowel disease.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherSociety for Experimental Biology and Medicine-
dc.titleDA-6034, a derivative of flavonoid, prevents and ameliorates dextran sulfate sodium-induced colitis and inhibits colon carcinogenesis-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.3181/0707-RM-186-
dc.identifier.scopusid2-s2.0-38949148964-
dc.identifier.wosid000252764500010-
dc.identifier.bibliographicCitationExperimental Biology and Medicine, v.233, no.2, pp 180 - 191-
dc.citation.titleExperimental Biology and Medicine-
dc.citation.volume233-
dc.citation.number2-
dc.citation.startPage180-
dc.citation.endPage191-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusULCERATIVE-COLITIS-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusEPITHELIAL-CELLS-
dc.subject.keywordPlusCYCLOOXYGENASE 2-
dc.subject.keywordPlusMURINE COLITIS-
dc.subject.keywordPlusANIMAL-MODELS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusRISK-
dc.subject.keywordAuthorDA-6034-
dc.subject.keywordAuthorinflammatory bowel disease-
dc.subject.keywordAuthorcolon cancer-
dc.identifier.urlhttps://journals.sagepub.com/doi/10.3181/0707-RM-186-
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