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Anti-inflammatory effects of BT-201, an n-butanol extract of Panax notoginseng, observed in vitro and in a collagen-induced arthritis model

DC Field Value Language
dc.contributor.authorChang, Sun-Hwa-
dc.contributor.authorChoi, Youngnim-
dc.contributor.authorPark, Jung-Ae-
dc.contributor.authorJung, Dong-Sik-
dc.contributor.authorShin, Jieun-
dc.contributor.authorYang, Ji-Hyun-
dc.contributor.authorKo, Seon-Yle-
dc.contributor.authorKim, Se-Won-
dc.contributor.authorKim, Jung-Keun-
dc.date.accessioned2023-04-19T07:06:20Z-
dc.date.available2023-04-19T07:06:20Z-
dc.date.created2021-04-14-
dc.date.issued2007-12-
dc.identifier.citationClinical Nutrition, Vol.26 No.6, pp.785-791-
dc.identifier.issn0261-5614-
dc.identifier.urihttps://hdl.handle.net/10371/190791-
dc.description.abstractBackground & aims: Although there has been some success with protein-based anti-tumor necrosis factor alpha (TNF-alpha) therapeutics, the problems associated with protein-based drugs demand alternative approaches. We screened various herbal. extracts for their ability to inhibit TNF-alpha secretions and found that BT-201, an n-butanol extract of Panax notoginseng (Burk.) F. H. Chen (P. notoginseng) has such an ability. Methods: The purpose of this study has been to evaluate the anti-inflammatory and antirheumatic effects of BT-201. The anti-inflammatory effects were evaluated by measuring the effects of BT-201 on the production of TNF-alpha, interleukin (IL)-1 ss, inducible nitric oxide (iNO), and matrix metalloproteinase- 13 (MMP-13), in vitro. The anti-rheumatic effects were evaluated by treating mice with collagen-induced arthritis (CIA) using a daily oral administration of BT-201 at 15 mg/kg/day. In addition, the effects on NF-kappa B and mitogen-activated protein kinase (MAPK) pathways were evaluated by Western blotting using phospho-specific antibodies. Results: BT-201 significantly inhibited all. the inflammatory parameters evaluated in vitro and delayed the onset and progression of CIA. BT-201 inhibited the activation of NF-kappa B, ERK, p38, and JNK pathways. Conclusions: Our results demonstrated that BT-201 can modulate various aspects of inflammation in vitro and that it has disease-modifying, anti-rheumatic effects in vivo,suggesting that it can be a potential alternative to the current anti-TNF-alpha therapeutics for rheumatoid arthritis and other inflammatory disease. (C) 2007 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.-
dc.language영어-
dc.publisherChurchill Livingstone-
dc.titleAnti-inflammatory effects of BT-201, an n-butanol extract of Panax notoginseng, observed in vitro and in a collagen-induced arthritis model-
dc.typeArticle-
dc.identifier.doi10.1016/j.clnu.2007.07.008-
dc.citation.journaltitleClinical Nutrition-
dc.identifier.wosid000251858200015-
dc.identifier.scopusid2-s2.0-36148941379-
dc.citation.endpage791-
dc.citation.number6-
dc.citation.startpage785-
dc.citation.volume26-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorChoi, Youngnim-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusRHEUMATOID-ARTHRITIS-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusTHERAPEUTIC STRATEGIES-
dc.subject.keywordPlusGINSENOSIDE RB-1-
dc.subject.keywordPlusORAL ABSORPTION-
dc.subject.keywordPlusTERMINAL KINASE-
dc.subject.keywordPlusDRUG-THERAPY-
dc.subject.keywordPlusVIVO MODELS-
dc.subject.keywordPlusDESTRUCTION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorPanax notoginseng-
dc.subject.keywordAuthorarthritis-
dc.subject.keywordAuthorTNF-alpha-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorMAPK-
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