Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-20021-z
Title: Distribution and accumulation of dietary ergothioneine and its metabolites in mouse tissues
Authors: Tang, R.M.Y 
Cheah, I.K.-M 
Yew, T.S.K 
Halliwell, B 
Keywords: antioxidant
thioneine
animal
animal structures
C57BL mouse
chemistry
liquid chromatography
male
oral drug administration
tandem mass spectrometry
Administration, Oral
Animal Structures
Animals
Antioxidants
Chromatography, Liquid
Ergothioneine
Male
Mice, Inbred C57BL
Tandem Mass Spectrometry
Issue Date: 2018
Publisher: Nature Publishing Group
Citation: Tang, 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
Abstract: L-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).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/174344
ISSN: 2045-2322
DOI: 10.1038/s41598-018-20021-z
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