Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17299
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dc.contributor.authorChayalak W.
dc.contributor.authorDeachapunya C.
dc.contributor.authorSuksamran S.
dc.contributor.authorPoonyachoti S.
dc.date.accessioned2022-03-10T13:16:46Z-
dc.date.available2022-03-10T13:16:46Z-
dc.date.issued2021
dc.identifier.issn17564646
dc.identifier.other2-s2.0-85117701600
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/17299-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85117701600&doi=10.1016%2fj.jff.2021.104814&partnerID=40&md5=42407813505c997a932a1ea550a5a1ec
dc.description.abstractHydroxyxanthones, the synthetic form of xanthones that predominantly found in mangosteen (Garcinia mangostana), have been indicated as a potent anti-inflammatory action. This study aimed to examine the action of various HDX forms in preventing a tight junction (TJ) barrier disruption induced by TNF-α or IL-1β through the inhibition of p-MLC expression in Caco-2 cell model. TJ barrier function was determined by transepithelial electrical resistance (TER) and flux measurement of fluorescein isothiocyanate-dextran (FD-4). 1-monoHDX or 1,3-diHDX (10 μM) promoted TER but not FD-4 permeability in the absence of cytokines. Pretreatment with 1-monoHDX at 10 μM for 24 h prevented TNF-α or IL-1β effect on TJ permeability. p-MLC protein expression by Western blot analysis, which was induced by IL-1β was inhibited with all HDXs. Tricyclic scaffold as the basic skeleton of all HDXs may be a potential candidate therapeutic for treatment of diseases-related leaky gut. © 2021
dc.languageen
dc.titleHydroxyxanthone ameliorates IL1β-induced epithelial barrier disruption in colonic-like cells by down-regulation of p-MLC expression
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of Functional Foods. Vol 87, No. (2021)
dc.identifier.doi10.1016/j.jff.2021.104814
Appears in Collections:Scopus 1983-2021

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