Abstract
The bioavailability of apigenin and its O-glycosides in humans was investigated with apigenin-4′-glucuronide (Ap-4′-GlcUA), apigenin-7-glucuronide and apigenin-7-sulfate being identified as in vivo metabolites. Apigenin per se was poorly absorbed with metabolites equivalent to 0.5% of intake excreted in urine 0–24 h post-intake. Consumption of a parsley drink containing apigenin-7-O-(2″-O-apiosyl)glucoside resulted in the peak plasma concentration (Cmax) of Ap-4′-GlcUA occurring after 4 h, indicative of absorption in the lower gastrointestinal tract (GIT). Urinary excretion of the three metabolites corresponded to 11.2% of intake. Ingestion of dried powdered parsley leaves with yogurt extended the Cmax of Ap-4′-GlcUA to 6 h. Consumption of chamomile tea containing apigenin-7′-O-glucoside resulted in a 2 h Cmax of Ap-4′-GlcUA, in keeping with absorption in the upper GIT. Urinary excretion was equivalent to 34% of intake. Intake of the parsley drink provided information on intra- and inter-individual variations in the level of excretion of the apigenin metabolites. Clinical trail registration number: This trail was registered at clinicaltrials.gov as NCT03526081.
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Borges, G., Fong, R. Y., Ensunsa, J. L., Kimball, J., Medici, V., Ottaviani, J. I., & Crozier, A. (2022). Absorption, distribution, metabolism and excretion of apigenin and its glycosides in healthy male adults. Free Radical Biology and Medicine, 185, 90–96. https://doi.org/10.1016/j.freeradbiomed.2022.04.007
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