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dc.contributor.authorShin, Ji Min-
dc.contributor.authorSon, Yang-Ju-
dc.contributor.authorHa, In Jin-
dc.contributor.authorErdenebileg, Saruul-
dc.contributor.authorJung, Da Seul-
dc.contributor.authorSong, Dae-geun-
dc.contributor.authorKim, Young Sik-
dc.contributor.authorKim, Sang Min-
dc.contributor.authorNho, Chu Won-
dc.date.accessioned2024-01-19T12:32:16Z-
dc.date.available2024-01-19T12:32:16Z-
dc.date.created2022-04-03-
dc.date.issued2022-03-
dc.identifier.issn2662-7671-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/115574-
dc.description.abstractBackground The incidence of inflammatory bowel disease (IBD), an inflammatory disorder of the gastrointestinal system has increased. IBD, characterized by aberrant immune responses against antigens, is thought to be caused by the invasion of enterobacteria. The pathogenesis of IBD is complicated, hence novel effective therapeutic agents are warranted. Therefore, this study evaluates the potential of Artemisia argyi, a medicinal herb, in alleviating IBD. Methods The effectiveness of the A. argyi ethanol extract was verified both in vitro and in vivo. Inflammation was induced in RAW 264.7 cells by 1 mu g/mL of lipopolysaccharide (LPS) and by 3% dextran sodium sulfate (DSS) in a DSS-induced colitis mouse model. During the ten-day colitis induction, 200 mg/kg of A. argyi ethanol extract was orally administered to the treatment group. Levels of inflammation-related proteins and genes were analyzed in the colon, serum, and lymphoid tissues, i.e., Peyer's patches (PPs) and spleen. The chemical constituent of the A. argyi ethanol extract was identified using an ultra-high performance liquid chromatography mass spectrometry (UPLC-MS/MS) analysis. Results A. argyi ethanol extract treatment ameliorated IBD symptoms and reduced the expression of inflammation-related proteins and genes in the colon and serum samples. Furthermore, A. argyi treatment induced the activation of anti-oxidative associated proteins, such as nuclear factor-erythroid factor 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1); and the treatment have also inhibited nuclear factor-kappa B (NF-kappa B), a central mediator of inflammatory responses. A. argyi enhanced the immunomodulatory effects in the PPs and spleen, which may stem from interleukin-10 (IL-10) upregulation. Chemical analysis identified a total of 28 chemical compounds, several of which have been reported to exert anti-inflammatory effects. Conclusions The effectiveness of the A. argyi ethanol extract in alleviating IBD was demonstrated; application of the extract successfully mitigated IBD symptoms, and enhanced immunomodulatory responses in lymphoid tissues. These findings suggest A. argyi as a promising herbal medicine for IBD treatment.-
dc.languageEnglish-
dc.publisherBMC-
dc.titleArtemisia argyi extract alleviates inflammation in a DSS-induced colitis mouse model and enhances immunomodulatory effects in lymphoid tissues-
dc.typeArticle-
dc.identifier.doi10.1186/s12906-022-03536-x-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBmc Complementary Medicine and Therapies, v.22, no.1-
dc.citation.titleBmc Complementary Medicine and Therapies-
dc.citation.volume22-
dc.citation.number1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000767799800002-
dc.identifier.scopusid2-s2.0-85126265082-
dc.relation.journalWebOfScienceCategoryIntegrative & Complementary Medicine-
dc.relation.journalResearchAreaIntegrative & Complementary Medicine-
dc.type.docTypeArticle-
dc.subject.keywordPlusBOWEL-DISEASE-
dc.subject.keywordPlusTHERAPEUTIC TARGETS-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusCYTOKINES-
dc.subject.keywordPlusSPLEEN-
dc.subject.keywordPlusINTERLEUKIN-10-
dc.subject.keywordPlusEPIDEMIOLOGY-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordAuthorInflammatory bowel diseases-
dc.subject.keywordAuthorArtemisia argyi-
dc.subject.keywordAuthorNatural products-
dc.subject.keywordAuthorSpleen-
dc.subject.keywordAuthorUPLC-MS-
dc.subject.keywordAuthorMS-
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