Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-20021-z
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dc.titleDistribution and accumulation of dietary ergothioneine and its metabolites in mouse tissues
dc.contributor.authorTang, R.M.Y
dc.contributor.authorCheah, I.K.-M
dc.contributor.authorYew, T.S.K
dc.contributor.authorHalliwell, B
dc.date.accessioned2020-09-04T02:19:58Z
dc.date.available2020-09-04T02:19:58Z
dc.date.issued2018
dc.identifier.citationTang, R.M.Y, Cheah, I.K.-M, Yew, T.S.K, Halliwell, B (2018). Distribution and accumulation of dietary ergothioneine and its metabolites in mouse tissues. Scientific Reports 8 (1) : 1601. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-20021-z
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174344
dc.description.abstractL-ergothioneine (ET) is a diet-derived amino acid that accumulates at high concentrations in animals and humans. Numerous studies have highlighted its antioxidant abilities in vitro, and possible cytoprotective capabilities in vivo. We investigated the uptake and distribution of ET in various organs by a highly sensitive and specific liquid chromatography coupled tandem mass spectrometry (LC-MS/MS) technique, both before and after oral administration of pure ET (35 and 70 mg/kg/day for 1, 7, and 28 days) to male C57BL6J mice. ET primarily concentrates in the liver and whole blood, and also in spleen, kidney, lung, heart, intestines, eye, and brain tissues. Strong correlations were found between ET and its putative metabolites - hercynine, ET-sulfonate (ET-SO3H), and S-methyl ET. Hercynine accumulates in the brain after prolonged ET administration. This study demonstrates the uptake and distribution of ET and provides a foundation for future studies with ET to target oxidative damage in a range of tissues in human diseases. © 2018 The Author(s).
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.subjectantioxidant
dc.subjectthioneine
dc.subjectanimal
dc.subjectanimal structures
dc.subjectC57BL mouse
dc.subjectchemistry
dc.subjectliquid chromatography
dc.subjectmale
dc.subjectoral drug administration
dc.subjecttandem mass spectrometry
dc.subjectAdministration, Oral
dc.subjectAnimal Structures
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectChromatography, Liquid
dc.subjectErgothioneine
dc.subjectMale
dc.subjectMice, Inbred C57BL
dc.subjectTandem Mass Spectrometry
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1038/s41598-018-20021-z
dc.description.sourcetitleScientific Reports
dc.description.volume8
dc.description.issue1
dc.description.page1601
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