Inhibitory effects of 3α-hydroxy-lup-20(29)-en-23, 28-dioic acid on lipopolysaccharide-induced TNF-α, IL-1β, and the high mobility group box 1 release in macrophages

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dc.contributor.authorX Q Liu-
dc.contributor.authorQ P Zou-
dc.contributor.authorJ J Huang-
dc.contributor.authorC S Yook-
dc.contributor.authorW K Whang-
dc.contributor.authorHyeong Kyu Lee-
dc.contributor.authorOk-Kyoung Kwon-
dc.date.accessioned2017-08-29-
dc.date.available2017-08-29-
dc.date.issued2017-
dc.identifier.issn0916-8451-
dc.identifier.uri10.1080/09168451.2017.1301803ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17214-
dc.description.abstractWe investigated the anti-inflammatory effects of 3α-hydroxy-lup-20(29)-en-23, 28-dioic acid (HLEDA) - a lupane-type triterpene isolated from leaves of Acanthopanax gracilistylus W. W. Smith (AGS), as well as the underlying molecular mechanisms in lipopolysaccharide (LPS)-induced RAW264.7 cells. Our results demonstrated that HLEDA concentration-dependently reduced the production of nitric oxide (NO), significantly suppressed LPS-induced expression of TNF-α and IL-1β at the mRNA and protein levels in RAW264.7 cells. Further analysis revealed that HLEDA could reduce the secretion of High Mobility Group Box 1 (HMGB1). Additionally, the results showed that HLEDA efficiently decreased nuclear factor-kappaB (NF-κB) activation by inhibiting the degradation and phosphorylation of IκBα. These results suggest that HLEDA exerts anti-inflammatory properties in LPS-induced macrophages, possibly through inhibition of the NF-κB signaling pathway, which mediates the expression of pro-inflammatory cytokines. These results warrant further studies that would concern candidate therapy for diseases, such as fulminant hepatitis and rheumatology of triterpenoids in AGS.-
dc.publisherT&F (Taylor & Francis)-
dc.titleInhibitory effects of 3α-hydroxy-lup-20(29)-en-23, 28-dioic acid on lipopolysaccharide-induced TNF-α, IL-1β, and the high mobility group box 1 release in macrophages-
dc.title.alternativeInhibitory effects of 3α-hydroxy-lup-20(29)-en-23, 28-dioic acid on lipopolysaccharide-induced TNF-α, IL-1β, and the high mobility group box 1 release in macrophages-
dc.typeArticle-
dc.citation.titleBioscience Biotechnology and Biochemistry-
dc.citation.number7-
dc.citation.endPage1313-
dc.citation.startPage1305-
dc.citation.volume81-
dc.contributor.affiliatedAuthorHyeong Kyu Lee-
dc.contributor.affiliatedAuthorOk-Kyoung Kwon-
dc.contributor.alternativeNameLiu-
dc.contributor.alternativeNameZou-
dc.contributor.alternativeNameHuang-
dc.contributor.alternativeName육창수-
dc.contributor.alternativeName황완균-
dc.contributor.alternativeName이형규-
dc.contributor.alternativeName권옥경-
dc.identifier.bibliographicCitationBioscience Biotechnology and Biochemistry, vol. 81, no. 7, pp. 1305-1313-
dc.identifier.doi10.1080/09168451.2017.1301803-
dc.subject.keyword3α-hydroxy-lup-20(29)-en-23,28-dioic acid-
dc.subject.keywordAnti-inflammatory-
dc.subject.keywordHMGB1-
dc.subject.keywordIL-1β-
dc.subject.keywordTNF-α-
dc.subject.local3α-hydroxy-lup-20(29)-en-23,28-dioic acid-
dc.subject.localAnti-inflammatory-
dc.subject.localanti-inflammatory-
dc.subject.localHMGB1-
dc.subject.localhigh mobility group box 1 (HMGB1)-
dc.subject.localIL-1β-
dc.subject.localIl-1β-
dc.subject.localTNF-a-
dc.subject.localTNF-alpha-
dc.subject.localTNF-α-
dc.subject.localTNFa-
dc.subject.localTNFα-
dc.subject.localTnf-α-
dc.subject.localTumor necrosis fa tor-α-
dc.subject.localTumor necrosis factor (TNF)-α-
dc.subject.localTumor necrosis factor alpha-
dc.subject.localTumor necrosis factor-alpha-
dc.subject.localTumor necrosis factor-α-
dc.subject.localtumor necrosis factor-alpha-
dc.subject.localtumor necrosis factor-α-
dc.description.journalClassY-
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Ochang Branch Institute > Division of National Bio-Infrastructure > Bio-Resource Central Bank > 1. Journal Articles
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