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Inhibitory Effect of Standardized Curcuma xanthorrhiza Supercritical Extract on LPS-Induced Periodontitis in Rats

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dc.contributor.authorKook, Kyo Eun-
dc.contributor.authorKim, Changhee-
dc.contributor.authorKang, Wonku-
dc.contributor.authorHwang, Jae-Kwan-
dc.date.available2019-01-22T12:37:49Z-
dc.date.issued2018-10-
dc.identifier.issn1017-7825-
dc.identifier.issn1738-8872-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/747-
dc.description.abstractPeriodontitis, which is a severe inflammatory disease caused by endotoxins secreted from oral pathogens, destructs gingival tissue and alveolar bone. Curcuma xanthorrhiza, commonly called Java turmeric, has been shown to possess anti-bacterial and anti-inflammatory activities. The present study evaluated the inhibitory effect of C. xanthorrhiza supercritical extract (CXS) standardized with xanthorrhizol on lipopolysaccharide (LPS)-induced periodontitis in an animal model. LPS was topically injected into the periodontium of Sprague-Dawley rats to induce periodontitis and CXS (30 and 100 mg.kg(-1).day(-1)) was orally administered after day 12. Histologically, CXS inhibited the collapse of gingival tissue by preventing cell infiltration. CXS significantly downregulated the expression of matrix metalloproteases (MMPs) and inflammation-related biomarkers, such as nuclear factor-kappa B (NF-kappa B) and interleukin-1 beta (IL-1 beta) in gingival tissue. CXS also improved bone remodeling by downregulating osteoclastic transcription factors, such as nuclear factor of activated T-cells c1 (NFATc1), tartrate-resistant acid phosphatase (TRAP), and cathepsin K. In addition, CXS upregulated osteoblast differentiation-related markers, alkaline phosphate (ALP) and collagen type I alpha (COLA1). Thus, CXS can ameliorate periodontitis by inhibiting inflammation and improving bone remodeling.-
dc.format.extent12-
dc.publisherKOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY-
dc.titleInhibitory Effect of Standardized Curcuma xanthorrhiza Supercritical Extract on LPS-Induced Periodontitis in Rats-
dc.typeArticle-
dc.identifier.doi10.4014/jmb.1808.08052-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.28, no.10, pp 1614 - 1625-
dc.identifier.kciidART002397940-
dc.description.isOpenAccessN-
dc.identifier.wosid000448398800004-
dc.identifier.scopusid2-s2.0-85065180574-
dc.citation.endPage1625-
dc.citation.number10-
dc.citation.startPage1614-
dc.citation.titleJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.volume28-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorCurcuma xanthorrhiza-
dc.subject.keywordAuthorosteoblastogenesis-
dc.subject.keywordAuthorosteoclastogenesis-
dc.subject.keywordAuthorperiodontitis-
dc.subject.keywordAuthorperiodontal inflammation-
dc.subject.keywordPlusHUMAN GINGIVAL FIBROBLASTS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusLIPOPOLYSACCHARIDE-
dc.subject.keywordPlusDIFFERENTIATION-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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