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Anti-inflammatory potential of peat moss extracts in lipopolysaccharide-stimulated RAW 264.7 macrophages

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dc.contributor.authorChoi, Woo-Suk-
dc.contributor.authorJeong, Jin-Woo-
dc.contributor.authorKim, Sung Ok-
dc.contributor.authorKim, Gi-Young-
dc.contributor.authorKim, Byung-Woo-
dc.contributor.authorKim, Cheol Min-
dc.contributor.authorSeo, Yong-Bae-
dc.contributor.authorKim, Woe-Yeon-
dc.contributor.authorLee, Sang-Yeol-
dc.contributor.authorJo, Kwon-Ho-
dc.contributor.authorChoi, Young Ju-
dc.contributor.authorChoi, Yung Hyun-
dc.contributor.authorKim, Gun-Do-
dc.date.accessioned2022-12-26T22:51:37Z-
dc.date.available2022-12-26T22:51:37Z-
dc.date.issued2014-10-
dc.identifier.issn1107-3756-
dc.identifier.issn1791-244X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18727-
dc.description.abstractThe aim of the present study was to identify the anti-inflammatory and anti-oxidative effects of peat moss aqueous extract (PME) on lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. To demonstrate the anti-inflammatory and antioxidant effects of PME, the levels of nitric oxide (NO) and cytokines were measured using Griess reagent and cytokine ELISA kits, respectively. Reverse transcriptase-polymerase chain reaction (RT-PCR) and western blot analysis were conducted to evaluate the expression of genes and proteins. Immunofluorescence was used to measure the expression and translocation of transcription factors. Pre-treatment with PME inhibited the production of prostaglandin E-2 and NO by suppressing the gene expression of cyclooxygenase-2 and inducible NO synthase, respectively. The LPS-stimulated gene expression and the production of tumor necrosis factor-alpha and interleukin-1 beta were significantly reduced by PME. In the LPS-stimulated RAW 264.7 cells, nuclear factor-kappa B (NF-kappa B) translocated from the cytosol to the nucleus, while pre-treatment with PME induced the sequestration of NF-kappa B in the cytosol through the inhibition of I kappa B alpha degradation. In the same manner, PME contributed to the inhibition of the activation of mitogen-activated protein kinases. In addition, the PME-treated RAW 264.7 cells facilitated the activation of nuclear factor-like 2 (Nrf2), and in turn, enhanced heme oxygenase-1 (HO-1) expression. These results indicate that PME exerts anti-inflammatory and antioxidant effects, and suggest that PME may neutralize inflammation and prevent cellular damage by oxidative stress.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherSPANDIDOS PUBL LTD-
dc.titleAnti-inflammatory potential of peat moss extracts in lipopolysaccharide-stimulated RAW 264.7 macrophages-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.doi10.3892/ijmm.2014.1881-
dc.identifier.scopusid2-s2.0-84907468566-
dc.identifier.wosid000342734500024-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, v.34, no.4, pp 1101 - 1109-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE-
dc.citation.volume34-
dc.citation.number4-
dc.citation.startPage1101-
dc.citation.endPage1109-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusHEME OXYGENASE-1-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusPOTASSIUM HUMATE-
dc.subject.keywordPlusINFLAMMATORY RESPONSES-
dc.subject.keywordPlusENDOTHELIAL-CELLS-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusMAP KINASES-
dc.subject.keywordAuthorpeat moss-
dc.subject.keywordAuthoranti-inflammation-
dc.subject.keywordAuthornuclear factor-kappa B-
dc.subject.keywordAuthormitogen-activated protein kinase-
dc.subject.keywordAuthornuclear factor-like 2/heme oxygenase-1-
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