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Plant sterol guggulsterone inhibits nuclear factor-kappa B signaling in intestinal epithelial cells by blocking I kappa B kinase and ameliorates acute murine colitis

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dc.contributor.authorCheon, Jae Hee-
dc.contributor.authorKim, Joo Sung-
dc.contributor.authorKim, Jung Mogg-
dc.contributor.authorKim, Nayoung-
dc.contributor.authorJung, Hyun Chae-
dc.contributor.authorSong, In Sung-
dc.date.accessioned2022-12-21T09:46:38Z-
dc.date.available2022-12-21T09:46:38Z-
dc.date.created2022-09-16-
dc.date.issued2006-12-
dc.identifier.issn1078-0998-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/180696-
dc.description.abstractBackground/Aims: The plant sterol guggulsterone has been shown to have anti-inflammatory properties. It remains unknown, however, whether guggulsterone is effective for the treatment of inflammatory bowel disease (IBD). Therefore, we investigated anti-inflammatory effects of guggulsterone on intestinal epithelial cells (IEC) and on experimental murine colitis models and elucidated its molecular mechanisms. Methods: Human Caco-2 cells and rat non-transformed IEC-18 cells were stimulated with interleukin (IL)-1 beta or lipopolysaccharide (LPS) with or without guggulsterone. The effects of guggulsterone on nuclear factor (NF)-kappa B signaling in IEC were examined by intercellular adhesion molecule (ICAM)-1 real-time reverse-transcription polymerase chain reaction, NF-kappa B transcriptional activity assay, Western blotting for I kappa B phosphorylation/degradation, electrophoretic mobility shift assay, and in vitro I kappa B kinase (IKK) assay For in vivo study, dextran sulfate sodium (DSS)-treated mice were fed with or without guggulsterone. Colitis was quantified by disease activity index and evaluation of macroscopic and microscopic findings. Phosphorylation Of I kappa B and IKK in colon mucosa was assessed by Western blotting and immunohistochemistry. Results: Guggulsterone significantly inhibited LPS- or IL-1 beta-induced ICAM-1 gene expression, NF-kappa B transcriptional activity, I kappa B phosphorylation/degradation, and NF-kappa B DNA binding activity in IEC. Moreover, guggulsterone strongly blocked IKK activity. Administration of guggulsterone significantly reduced the severity of DSS-induced murine colitis as assessed by clinical disease activity score, colon length, and histology Furthermore, tissue upregulation of I kappa B and IKK phosphorylation induced by DSS was attenuated in guggulsterone-treated mice. Conclusion: Guggulsterone blocks NF-kappa B signaling pathway by targeting IKK complex in IEC and attenuates DSS-induced acute murine colitis, which suggests that guggulsterone could be an attractive therapeutic option in the treatment of IBD.-
dc.language영어-
dc.language.isoen-
dc.publisherOXFORD UNIV PRESS INC-
dc.titlePlant sterol guggulsterone inhibits nuclear factor-kappa B signaling in intestinal epithelial cells by blocking I kappa B kinase and ameliorates acute murine colitis-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jung Mogg-
dc.identifier.doi10.1097/01.mib.0000235830.94057.c6-
dc.identifier.scopusid2-s2.0-33751577977-
dc.identifier.wosid000242391600009-
dc.identifier.bibliographicCitationINFLAMMATORY BOWEL DISEASES, v.12, no.12, pp.1152 - 1161-
dc.relation.isPartOfINFLAMMATORY BOWEL DISEASES-
dc.citation.titleINFLAMMATORY BOWEL DISEASES-
dc.citation.volume12-
dc.citation.number12-
dc.citation.startPage1152-
dc.citation.endPage1161-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusPROINFLAMMATORY GENE-EXPRESSION-
dc.subject.keywordPlusTUMOR-NECROSIS-FACTOR-
dc.subject.keywordPlusINFLAMMATORY RESPONSES-
dc.subject.keywordPlusCOMMIPHORA MUKUL-
dc.subject.keywordPlusIKK-BETA-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusALPHA-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusCHOLESTEROL-
dc.subject.keywordAuthorguggulsterone-
dc.subject.keywordAuthornuclear factor-kappa B-
dc.subject.keywordAuthorI kappa B kinase-
dc.subject.keywordAuthorinflammatory bowel disease-
dc.identifier.urlhttps://academic.oup.com/ibdjournal/article/12/12/1152/4682864-
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