Absorption, metabolism, and excretion of fermented orange juice (poly)phenols in rats

• Published in: BioFactors (Oxford) Vol. 40; no. 3; pp. 327 - 335
• Main Authors: Escudero-López, Blanca, Calani, Luca, Fernández-Pachón, María-Soledad, Ortega, Ángeles, Brighenti, Furio, Crozier, Alan, Del Rio, Daniele
• Format: Journal Article
• Language: English
• Published: Netherlands Blackwell Publishing Ltd 01.05.2014
• Subjects: Administration, Oral; Animals; Beverages; bioavailability; Citrus; Citrus sinensis - chemistry; colon microbiota; Fermentation; flavanones; Fruit - chemistry; Gastrointestinal Absorption; hydroxycinnamates; Male; orange juice; Plant Extracts - administration & dosage; Plant Extracts - pharmacokinetics; Polyphenols - administration & dosage; Polyphenols - pharmacokinetics; rats; Rats, Wistar; urinary excretion; orange juice; hydroxycinnamates; urinary excretion; bioavailability; colon microbiota; rats; flavanones
• ISSN: 0951-6433; 1872-8081
• DOI: 10.1002/biof.1152

Two milliliters of a fermented, pasteurized orange juice containing ∼1% alcohol and 2.3 μmol of (poly)phenolic compounds was fed to rats by gavage after which plasma and urine collected over a 36 h period were analyzed by UHPLC‐mass spectrometry. The main constituents in the juice were hesperetin and naringenin‐O‐glycosides, apigenin‐6,8‐C‐diglucoside, and ferulic acid‐4′‐O‐glucoside. Plasma contained seven flavanone glucuronides, with the principal metabolites, naringenin‐7‐O‐glucuronide, naringenin‐4′‐O‐glucuronide, and an isosakuranetin‐O‐glucuronide, peaking 6 h after intake at concentrations of ∼10 nmol/L. Urinary excretion of four hesperetin glucuronides was equivalent to 0.28% of intake while that of the two naringenin glucuronides was 2.8% of intake. The plasma and urine data suggest that while some absorption occurred in the small intestine, the main site of uptake was the colon. Urine also contained dihydroferulic acid‐4'‐O‐glucuronide and dihydroferulic acid‐4′‐O‐sulfate which were excreted in quantities corresponding to 48.2% of the ingested ferulic acid‐4′‐glucoside. This indicates that the hydroxycinnamate is much more bioavailable than the flavanones in the rat model. Conversion of the ferulic acid glucoside to the dihydroferulic acid metabolites involves the action of colonic microbial glycosidases and reductases/hydrogenases followed by postabsorption phase II metabolism before renal excretion. © 2013 BioFactors, 40(3):327–335, 2014