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dc.contributor.authorWachiraporn Luerangen_US
dc.contributor.authorThongchai Khammeeen_US
dc.contributor.authorWatinee Kumpumen_US
dc.contributor.authorSunit Suksamrarnen_US
dc.contributor.authorVaranuj Chatsudthipongen_US
dc.contributor.authorChatchai Muanprasaten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherGraduate Program in Toxicologyen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.date.accessioned2018-06-11T04:36:06Z-
dc.date.available2018-06-11T04:36:06Z-
dc.date.issued2012-06-27en_US
dc.identifier.citationLife Sciences. Vol.90, No.25-26 (2012), 988-994en_US
dc.identifier.issn18790631en_US
dc.identifier.issn00243205en_US
dc.identifier.other2-s2.0-84863314622en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84863314622&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/13692-
dc.description.abstractAims: Previous investigation showed that polyphenols abundantly found in many plants could inhibit Cl - secretion. The present study was aimed to investigate the effect of phenol containing xanthone derivatives on cAMP-activated intestinal Cl - secretion and evaluate potential benefits of these compounds in the treatment of cholera. Main methods: Four hydroxy xanthones were synthesized via oxidative coupling reaction of the corresponding ortho-hydroxybenzoic acids and hydroxyphenols. Short-circuit current and apical Cl - current measurements across monolayers of human intestinal epithelial (T84) cell and Fisher rat thyroid cells transfected with human CFTR (FRT-hCFTR cell) were performed to determine the effect of hydroxyxanthones on cAMP-activated Cl - secretion. Intracellular cAMP was measured by immunoassay methods. Anti-diarrheal efficacy was evaluated using closed loop model of cholera. Key findings: Among the tested xanthones, 1,3,6-trihydroxyxanthone (THX-001) was found to be the most potent derivative in the inhibition of cAMP-activated Cl - secretion across T84 cell monolayers (IC 50 ~ 100 μM). Electrophysiological analysis of T84 cells and FRT-hCFTR cells revealed that THX-001 targeted two distinct cAMP-activated Cl - channels in the apical membrane of T84 cells, namely, CFTR and inward rectifying Cl - channel (IRC). In contrast, THX-001 had no effect on intracellular cAMP levels in these cells. Importantly, THX-001 completely abolished cholera toxin-induced Cl - secretion across T84 cell monolayers and significantly inhibited cholera toxin-induced intestinal fluid secretion in mouse closed loop models. Significance: This study revealed that hydroxyxanthone represents another chemical class of polyphenolic compounds that may hold promise as anti-secretory therapy for cholera. © 2012 Elsevier Inc.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84863314622&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleHydroxyxanthone as an inhibitor of cAMP-activated apical chloride channel in human intestinal epithelial cellen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.lfs.2012.05.001en_US
Appears in Collections:Scopus 2011-2015

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