Free Radical Research 2002-11-01

The metabolism of dietary polyphenols and the relevance to circulating levels of conjugated metabolites.

Andreas R Rechner, Gunter Kuhnle, Henglong Hu, Andrea Roedig-Penman, Maarten H van den Braak, Kevin P Moore, Catherine A Rice-Evans

Index: Free Radic. Res. 36(11) , 1229-41, (2002)

Full Text: HTML

Abstract

Berry extracts rich in anthocyanins have been linked to protective effects including the modulation of age-related neurological dysfunction and the improvement of the resistance of red blood cells against oxidative stress in vitro. In this study the bioavailability, metabolism and elimination of polyphenols from blackcurrant juice, rich in anthocyanins, flavonols, and hydroxycinnamates, were investigated. The four major native anthocyanidin glycosides of blackcurrant juice, delphinidin-3-glucoside, delphinidin-3-rutinoside, cyanidin-3-glucoside and cyanidin-3-rutinoside, were detected and identified in low amounts by HPLC and LC-MS in plasma and urine post-ingestion. Elimination of the anthocyanins was fast (maximum excretion after 1 h) and plasma levels (0-128.6 nmol/l) and total urinary exretion (0.07-1.35 mg; 0.007-0.133% of the dose ingested) were low. Most significantly, of the hydroxycinnamates, conjugated and free ferulic, isoferulic, p-coumaric, sinapic and vanillic acids were identified in plasma and urine, using GC-MS techniques. Quercetin and kaempferol (as glucuronides) and the proposed colonic metabolite of quercetin, 3-hydroxyphenylacetic acid, were detectable in a minority of subjects. Increased daily urinary hippuric, 4-hydroxyhippuric and 3-hydroxyhippuric acid levels were also observed post-ingestion in all volunteers.

Related Compounds

Structure Name/CAS No. Articles
3-Hydroxyphenylacetic acid Structure 3-Hydroxyphenylacetic acid
CAS:621-37-4
Vanillic acid Structure Vanillic acid
CAS:121-34-6
Delphinidin chloride Structure Delphinidin chloride
CAS:528-53-0
Isoferulic acid Structure Isoferulic acid
CAS:537-73-5