Publication:
An ethyl-acetate fraction of Holothuria scabra modulates inflammation in vitro through inhibiting the production of nitric oxide and pro-inflammatory cytokines via NF-κB and JNK pathways

dc.contributor.authorPranweerapaiboon K.
dc.contributor.authorApisawetakan S.
dc.contributor.authorNobsathian S.
dc.contributor.authorItharat A.
dc.contributor.authorSobhon P.
dc.contributor.authorChaithirayanon K.
dc.date.accessioned2021-04-05T03:01:20Z
dc.date.available2021-04-05T03:01:20Z
dc.date.issued2020
dc.date.issuedBE2563
dc.description.abstractSea cucumber, Holothuria scabra, is an echinoderm marine animal that has long been used as a traditional therapeutic in various diseases due to its chemical composition and protein enrichment. Many researchers have extensively studied the efficacy of sea cucumber extracts for many health benefits in recent years. Inflammation is a complex process involved in pro-/anti-inflammatory cytokine products. However, the role of the H. scabra extracts in anti-inflammation and its molecular regulations has not been apparently elucidated yet. In this study, we investigated the anti-inflammatory effect of H. scabra extracts by using lipopolysaccharide (LPS) from E. coli to induce an inflammatory response in RAW264.7 macrophage. It was found that ethyl acetate fraction of H. scabra extracts (EAHS) inhibited pro-inflammatory cytokines synthesis at both the transcriptional and translational levels, notably nitric oxide (NO), inducible nitric oxide synthase (iNOS), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and prostaglandin E2 (PGE2). In addition, EAHS was able to downregulate IκB/NF-κB, and JNK expressions. These effects may be influenced by high contents of phenolic compound and triterpene glycosides in EAHS. Therefore, EAHS might have the potential to be developed as a natural anti-inflammatory agent. © 2019, Springer Nature Switzerland AG.
dc.format.mimetypeapplication/pdf
dc.identifier.citationInflammopharmacology. Vol 28, No.4 (2020), p.1027-1037
dc.identifier.doi10.1007/s10787-019-00677-3
dc.identifier.issn9254692
dc.identifier.other2-s2.0-85076098030
dc.identifier.urihttps://swu-dspace2.eval.plus/handle/123456789/4461
dc.rights.holderScopus
dc.subject.otherAcetic acid ethyl ester
dc.subject.otherAnimal extract
dc.subject.otherAntiinflammatory agent
dc.subject.otherButanol
dc.subject.otherCytokine
dc.subject.otherGallic acid
dc.subject.otherGlycoside
dc.subject.otherHexane
dc.subject.otherHolothuria scabra extract
dc.subject.otherI kappa B
dc.subject.otherImmunoglobulin enhancer binding protein
dc.subject.otherInducible nitric oxide synthase
dc.subject.otherInterleukin 1beta
dc.subject.otherJanus kinase
dc.subject.otherLipopolysaccharide
dc.subject.otherMessenger RNA
dc.subject.otherMitogen activated protein kinase p38
dc.subject.otherNitric oxide
dc.subject.otherPhenol derivative
dc.subject.otherProstaglandin E2
dc.subject.otherSTAT3 protein
dc.subject.otherTerpene
dc.subject.otherTriterpene
dc.subject.otherTumor necrosis factor
dc.subject.otherUnclassified drug
dc.subject.otherAnimal cell
dc.subject.otherAntiinflammatory activity
dc.subject.otherArticle
dc.subject.otherCell viability assay
dc.subject.otherComparative study
dc.subject.otherControlled study
dc.subject.otherCytokine production
dc.subject.otherCytokine release
dc.subject.otherCytotoxicity
dc.subject.otherDown regulation
dc.subject.otherDrug megadose
dc.subject.otherEnzyme linked immunosorbent assay
dc.subject.otherHolothuria
dc.subject.otherHolothuria scabra
dc.subject.otherIn vitro study
dc.subject.otherMRNA expression level
dc.subject.otherMTT assay
dc.subject.otherNonhuman
dc.subject.otherPriority journal
dc.subject.otherProtein expression
dc.subject.otherProtein phosphorylation
dc.subject.otherProton nuclear magnetic resonance
dc.subject.otherRAW 264.7 cell line
dc.titleAn ethyl-acetate fraction of Holothuria scabra modulates inflammation in vitro through inhibiting the production of nitric oxide and pro-inflammatory cytokines via NF-κB and JNK pathways
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85076098030&doi=10.1007%2fs10787-019-00677-3&partnerID=40&md5=10de9e5886bc049b19960a6299016caa

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