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In vivo biotransformation of (poly)phenols and anthocyanins of red-fleshed apple and identification of intake biomarkers

[Display omitted] •Red-flesh apples as a novel anthocyanin rich food.•Complete metabolic pathways for phenolics from red-flesh apples.•Phloretin glucuronide as specific apple intake biomarker.•Cyanidin galactoside and peonidin galactoside as red-flesh apple intake biomarkers. The aim of this study w...

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Bibliographic Details
Published in:Journal of functional foods 2019-04, Vol.55, p.146-155
Main Authors: Yuste, Silvia, Ludwig, Iziar A., Rubió, Laura, Romero, Maria-Paz, Pedret, Anna, Valls, Rosa-Maria, Solà, Rosa, Motilva, Maria-José, Macià, Alba
Format: Article
Language:English
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Summary:[Display omitted] •Red-flesh apples as a novel anthocyanin rich food.•Complete metabolic pathways for phenolics from red-flesh apples.•Phloretin glucuronide as specific apple intake biomarker.•Cyanidin galactoside and peonidin galactoside as red-flesh apple intake biomarkers. The aim of this study was to investigate comprehensively the metabolic pathways and human bioavailability of anthocyanins and other (poly)phenols in an apple matrix, and to elucidate potential intake biomarkers. After the acute intake of a red-fleshed apple freeze-dried snack, plasma and urine were collected and analyzed by UPLC-MS/MS. A total of 37 phase-II and microbial phenolic metabolites were detected in plasma and urine. Among these, phloretin glucuronide, cyanidin-3-O-galactoside (plasma and urine) and peonidin-3-O-galactoside (urine) were the only metabolites detected in all the volunteers and not detected at basal conditions. The maximum urine excretion was detected at 2–4 h, and the main increase in plasma of phloretin glucuronide and cyanidin-3-O-galactoside was observed at 2 h post-intake (61.0 ± 6.82 and 10.3 ± 1.50 nM, respectively). These metabolites could be selected as the best intake biomarkers of red-fleshed apple and might be useful in human intervention studies when studying its health effects.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2019.02.013