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Evaluation of Anti-Colitic Effect of Chung-Jang-Hwan (C-mix) in Mice

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dc.contributor.authorLee, Hoyong-
dc.contributor.authorAhn, Young-Tae-
dc.contributor.authorPark, Se-Hoon-
dc.contributor.authorAhn, Young Min-
dc.contributor.authorShim, Jae-Jung-
dc.contributor.authorLee, Jung-Hee-
dc.contributor.authorLee, Jeong-Sang-
dc.contributor.authorSurh, Young-Joon-
dc.contributor.authorHuh, Chul-Sung-
dc.contributor.authorKim, Dong-Hyun-
dc.date.accessioned2021-01-31T09:24:12Z-
dc.date.available2021-01-31T09:24:12Z-
dc.date.created2017-11-15-
dc.date.created2017-11-15-
dc.date.issued2011-01-
dc.identifier.citationBiomolecules & Therapeutics, Vol.19 No.1, pp.52-58-
dc.identifier.issn1976-9148-
dc.identifier.other2387-
dc.identifier.urihttps://hdl.handle.net/10371/172643-
dc.description.abstractThe inhibitory effect of Chung-Jang-Hwan (C-mix) consisted of Geranium nepalense subsp. thunbergii, Saururus chinensis, and Rubus coreanus were investigated in dextran sulfate sodium (DSS)-induced colitic mice by microarray analysis. Treatment with C-mix improved colitic symptoms, including colon shortening and myeloperoxidase activity. Treatment with DSS alone upregulated the expression levels of inflammation-related genes, including IL-1 beta, IL-6, CCL2, CCL4, CCL5, CCL7, CCL8, CCL24, CXCL1, CXCL2, CXCL5, CXCL9 and CXCL10, and other colitis-related genes such as COX-2, PAP, MMP family, S100a8, S100a9 and DEFA1 in mice. However, treatment with C-mix inhibited the expression levels of inflammation-associated genes induced by DSS. The increased expression levels of COX-2 and IL-1 beta, representative inflammatory genes, were confirmed by a quantitative real-time polymerase chain reaction analysis. These results indicate that C-mix may ameliorate colitis by the inhibitory regulation of inflammation-associated genes.-
dc.language영어-
dc.publisher한국응용약물학회-
dc.titleEvaluation of Anti-Colitic Effect of Chung-Jang-Hwan (C-mix) in Mice-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.4062/biomolther.2011.19.1.052-
dc.citation.journaltitleBiomolecules & Therapeutics-
dc.identifier.wosid000288108200008-
dc.identifier.scopusid2-s2.0-79851486878-
dc.citation.endpage58-
dc.citation.number1-
dc.citation.startpage52-
dc.citation.volume19-
dc.identifier.sci000288108200008-
dc.identifier.kciidART001522623-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.contributor.affiliatedAuthorHuh, Chul-Sung-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusINFLAMMATORY-BOWEL-DISEASE-
dc.subject.keywordPlusULCERATIVE-COLITIS-
dc.subject.keywordPlusINCREASED EXPRESSION-
dc.subject.keywordPlusANTISENSE OLIGONUCLEOTIDE-
dc.subject.keywordPlusCHEMOKINE EXPRESSION-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusRUBUS-COREANUS-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordPlusCXC-
dc.subject.keywordPlusPROFILES-
dc.subject.keywordAuthorChung-Jang-Hwan-
dc.subject.keywordAuthorC-mix-
dc.subject.keywordAuthorColitis-
dc.subject.keywordAuthorInflammation-
dc.subject.keywordAuthorMicroarray-
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  • Department of Pharmacy
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