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dc.contributor.author Jeong, Jin-Woo -
dc.contributor.author Lee, Hye Hyeon -
dc.contributor.author Han, Min Ho -
dc.contributor.author Kim, Gi-Young -
dc.contributor.author Hong, Su Hyun -
dc.contributor.author Park, Cheol -
dc.contributor.author Choi, Yung Hyun -
dc.date.available 2017-07-11T06:22:37Z -
dc.date.created 2017-04-10 -
dc.date.issued 2014-03 -
dc.identifier.issn 1472-6882 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/3107 -
dc.description.abstract Background: Poria cocos Wolf, a medicinal fungus, is widely used in traditional medicines in East Asian countries owing to its various therapeutic potentials. Although several studies have demonstrated the anti-inflammatory activity of this fungus, its underlying mechanisms have not yet been clearly defined.Methods: In the present study, we have demonstrated the anti-inflammatory effects of ethanol extract of P. cocos (EEPC) in lipopolysaccaride (LPS)-stimulated RAW 264.7 macrophages. As inflammatory parameters, the productions of nitric oxide (NO), prostaglandin E2 (PGE2), interleukin (IL)-1β and tumor necrosis factor (TNF)-α were evaluated. We also examined the EEPC's effect on the nuclear factor-kappaB (NF-κB) signaling pathway.Results: Our results indicated that EEPC exhibits a potent inhibitory effect on NO production and inhibits PGE2 release in LPS-induced macrophages without affecting cell viability. EEPC also significantly attenuated LPS-induced secretion of inflammatory cytokines IL-1β and TNF-α. Additionally, LPS-induced expression of inducible NO synthase (iNOS), cyclooxygenase (COX)-2, IL-1β, and TNF-α was decreased by pre-treatment with EEPC at the transcriptional level. Moreover, EEPC clearly inhibited LPS-induced nuclear translocation of NF-κB p65 subunits, which correlated with EEPC's inhibitory effects on inhibitor kappaB (IκB) degradation. Moreover, EEPC clearly suppressed the LPS-induced DNA-binding activity of NF-κB, as well as the nuclear translocation of the NF-κB p65, which correlated with EEPC's inhibitory effects on inhibitor kappaB (IκB) degradation.Conclusions: Taken together, our data indicates that EEPC targets the inflammatory response of macrophages via inhibition of iNOS, COX-2, IL-1β, and TNF-α through inactivation of the NF-κB signaling pathway, supporting the pharmacological basis of P. cocos as a traditional herbal medicine for treatment of inflammation and its associated disorders. © 2014 Jeong et al.; licensee BioMed Central Ltd. -
dc.language English -
dc.publisher BioMed Central Ltd. -
dc.title Ethanol extract of Poria cocos reduces the production of inflammatory mediators by suppressing the NF-kappaB signaling pathway in lipopolysaccharide-stimulated RAW 264.7 macrophages -
dc.type Article -
dc.identifier.doi 10.1186/1472-6882-14-101 -
dc.identifier.scopusid 2-s2.0-84899135480 -
dc.identifier.bibliographicCitation BMC Complementary and Alternative Medicine, v.14 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor Poria cocos -
dc.subject.keywordAuthor RAW 264.7 cells -
dc.subject.keywordAuthor Anti-inflammation -
dc.subject.keywordAuthor NF-kappa B -
dc.subject.keywordPlus ANTIINFLAMMATORY ACTIVITY -
dc.subject.keywordPlus ANTIOXIDANT ACTIVITIES -
dc.subject.keywordPlus PROSTAGLANDIN E-2 -
dc.subject.keywordPlus CANCER -
dc.subject.keywordPlus CELLS -
dc.subject.keywordPlus CYCLOOXYGENASE-2 -
dc.subject.keywordPlus TRITERPENES -
dc.subject.keywordPlus PROGRESSION -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus DERMATITIS -
dc.citation.title BMC Complementary and Alternative Medicine -
dc.citation.volume 14 -
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