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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.authorKanta Pranweerapaiboonen_US
dc.contributor.authorSomjai Apisawetakanen_US
dc.contributor.authorSaksit Nobsathianen_US
dc.contributor.authorArunporn Itharaten_US
dc.contributor.authorPrasert Sobhonen_US
dc.contributor.authorKulathida Chaithirayanonen_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherBurapha Universityen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.date.accessioned2020-01-27T09:05:40Z
dc.date.available2020-01-27T09:05:40Z
dc.date.issued2019-01-01en_US
dc.description.abstract© 2019, Springer Nature Switzerland AG. Sea 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.en_US
dc.identifier.citationInflammopharmacology. (2019)en_US
dc.identifier.doi10.1007/s10787-019-00677-3en_US
dc.identifier.issn15685608en_US
dc.identifier.issn09254692en_US
dc.identifier.other2-s2.0-85076098030en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51156
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85076098030&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
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 pathwaysen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85076098030&origin=inwarden_US

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