Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/11873
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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.identifier.issn9254692
dc.identifier.other2-s2.0-85076098030
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/11873-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85076098030&doi=10.1007%2fs10787-019-00677-3&partnerID=40&md5=10de9e5886bc049b19960a6299016caa
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.subjectacetic acid ethyl ester
dc.subjectanimal extract
dc.subjectantiinflammatory agent
dc.subjectbutanol
dc.subjectcytokine
dc.subjectgallic acid
dc.subjectglycoside
dc.subjecthexane
dc.subjectHolothuria scabra extract
dc.subjectI kappa B
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinducible nitric oxide synthase
dc.subjectinterleukin 1beta
dc.subjectJanus kinase
dc.subjectlipopolysaccharide
dc.subjectmessenger RNA
dc.subjectmitogen activated protein kinase p38
dc.subjectnitric oxide
dc.subjectphenol derivative
dc.subjectprostaglandin E2
dc.subjectSTAT3 protein
dc.subjectterpene
dc.subjecttriterpene
dc.subjecttumor necrosis factor
dc.subjectunclassified drug
dc.subjectanimal cell
dc.subjectantiinflammatory activity
dc.subjectArticle
dc.subjectcell viability assay
dc.subjectcomparative study
dc.subjectcontrolled study
dc.subjectcytokine production
dc.subjectcytokine release
dc.subjectcytotoxicity
dc.subjectdown regulation
dc.subjectdrug megadose
dc.subjectenzyme linked immunosorbent assay
dc.subjectHolothuria
dc.subjectHolothuria scabra
dc.subjectin vitro study
dc.subjectmRNA expression level
dc.subjectMTT assay
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectprotein phosphorylation
dc.subjectproton nuclear magnetic resonance
dc.subjectRAW 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
dc.rights.holderScopus
dc.identifier.bibliograpycitationInflammopharmacology. Vol 28, No.4 (2020), p.1027-1037
dc.identifier.doi10.1007/s10787-019-00677-3
Appears in Collections:Scopus 1983-2021

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