DC Field | Value | Language |
---|---|---|
dc.contributor.author | X Q Liu | - |
dc.contributor.author | Q P Zou | - |
dc.contributor.author | J J Huang | - |
dc.contributor.author | C S Yook | - |
dc.contributor.author | W K Whang | - |
dc.contributor.author | Hyeong Kyu Lee | - |
dc.contributor.author | Ok-Kyoung Kwon | - |
dc.date.accessioned | 2017-08-29 | - |
dc.date.available | 2017-08-29 | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0916-8451 | - |
dc.identifier.uri | 10.1080/09168451.2017.1301803 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/17214 | - |
dc.description.abstract | We 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.publisher | T&F (Taylor & Francis) | - |
dc.title | 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 | - |
dc.title.alternative | 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 | - |
dc.type | Article | - |
dc.citation.title | Bioscience Biotechnology and Biochemistry | - |
dc.citation.number | 7 | - |
dc.citation.endPage | 1313 | - |
dc.citation.startPage | 1305 | - |
dc.citation.volume | 81 | - |
dc.contributor.affiliatedAuthor | Hyeong Kyu Lee | - |
dc.contributor.affiliatedAuthor | Ok-Kyoung Kwon | - |
dc.contributor.alternativeName | Liu | - |
dc.contributor.alternativeName | Zou | - |
dc.contributor.alternativeName | Huang | - |
dc.contributor.alternativeName | 육창수 | - |
dc.contributor.alternativeName | 황완균 | - |
dc.contributor.alternativeName | 이형규 | - |
dc.contributor.alternativeName | 권옥경 | - |
dc.identifier.bibliographicCitation | Bioscience Biotechnology and Biochemistry, vol. 81, no. 7, pp. 1305-1313 | - |
dc.identifier.doi | 10.1080/09168451.2017.1301803 | - |
dc.subject.keyword | 3α-hydroxy-lup-20(29)-en-23,28-dioic acid | - |
dc.subject.keyword | Anti-inflammatory | - |
dc.subject.keyword | HMGB1 | - |
dc.subject.keyword | IL-1β | - |
dc.subject.keyword | TNF-α | - |
dc.subject.local | 3α-hydroxy-lup-20(29)-en-23,28-dioic acid | - |
dc.subject.local | Anti-inflammatory | - |
dc.subject.local | anti-inflammatory | - |
dc.subject.local | HMGB1 | - |
dc.subject.local | high mobility group box 1 (HMGB1) | - |
dc.subject.local | IL-1β | - |
dc.subject.local | Il-1β | - |
dc.subject.local | TNF-a | - |
dc.subject.local | TNF-alpha | - |
dc.subject.local | TNF-α | - |
dc.subject.local | TNFa | - |
dc.subject.local | TNFα | - |
dc.subject.local | Tnf-α | - |
dc.subject.local | Tumor necrosis fa tor-α | - |
dc.subject.local | Tumor necrosis factor (TNF)-α | - |
dc.subject.local | Tumor necrosis factor alpha | - |
dc.subject.local | Tumor necrosis factor-alpha | - |
dc.subject.local | Tumor necrosis factor-α | - |
dc.subject.local | tumor necrosis factor-alpha | - |
dc.subject.local | tumor necrosis factor-α | - |
dc.description.journalClass | Y | - |
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