Publication:
Protective effect of diarylheptanoids from Curcuma comosa on primary rat hepatocytes against t-butyl hydroperoxide-induced toxicity

dc.contributor.authorKanoknetr Suksenen_US
dc.contributor.authorTumnoon Charaslertrangsien_US
dc.contributor.authorChadanat Nooninen_US
dc.contributor.authorSurawat Jariyawaten_US
dc.contributor.authorWatcharaporn Devakul Na Ayutthayaen_US
dc.contributor.authorApichart Suksamrarnen_US
dc.contributor.authorPatoomratana Tuchindaen_US
dc.contributor.authorPawinee Piyachaturawaten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherRangsit Universityen_US
dc.contributor.otherRamkhamhaeng Universityen_US
dc.date.accessioned2018-12-11T02:15:43Z
dc.date.accessioned2019-03-14T08:04:06Z
dc.date.available2018-12-11T02:15:43Z
dc.date.available2019-03-14T08:04:06Z
dc.date.issued2016-05-03en_US
dc.description.abstract© 2015 Taylor & Francis. Context: Curcuma comosa Roxb. (Zingiberaceae) has traditionally been used as an anti-inflammatory agent in liver, and recent study has shown its hepatoprotective effect against CCl4-induced liver injury in vivo.Objective: This study further assesses the protective effect of C. comosa extracts and its isolated compounds against tert-butyl hydroperoxide (t-BHP)-induced hepatotoxicity in isolated primary rat hepatocytes.Materials and methods: Isolated primary hepatocytes were pretreated with either ethanol (5-50 g/ml) or hexane extract (1-50 g/ml), or two diarylheptanoids (4-35 M): compound D-91 [1-(4-hydroxyphenyl)-7-phenyl-(6E)-6-hepten-3-ol] and compound D-92 [(3S)-1-(3,4-dihydroxyphenyl)-7-phenyl-(6E)-6-hepten-3-ol], from C. comosa for 2 h prior to exposure to 1.5 mM t-BHP for 15 and 30 min. Their hepatoprotective activities were then determined.Results: t-BHP markedly caused the formation of MDA and ALT leakage from the hepatocytes. Pretreatment with the C. comosa ethanol extract showed greater protective effect than the hexane extract, and the effect was concentration related. Treating the hepatocytes with compound D-92 provided greater protective effect than compound D-91. IC50values of compounds D-91, D-92, and silymarin for the protection of ALT leakage at 30 min were 32.7 ± 1.1, 9.8 ± 0.7, and 160 ± 8 M, respectively. Further investigation showed that compound D-92 was more effective in maintaining the intracellular glutathione content in the t-BHP treated group, whereas the reduction in antioxidant enzymes, glutathione peroxidase and glutathione-S-transferase activities, were not improved.Discussion and conclusion: Results suggest that diarylheptanoids are the active principles that provide protection against t-BHP-induced injury. Their ability to maintain intracellular glutathione content is the main mechanisms underlying the protective action.en_US
dc.identifier.citationPharmaceutical Biology. Vol.54, No.5 (2016), 853-862en_US
dc.identifier.doi10.3109/13880209.2015.1088550en_US
dc.identifier.issn17445116en_US
dc.identifier.issn13880209en_US
dc.identifier.other2-s2.0-84960393000en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43039
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84960393000&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleProtective effect of diarylheptanoids from Curcuma comosa on primary rat hepatocytes against t-butyl hydroperoxide-induced toxicityen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84960393000&origin=inwarden_US

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