Platelet-Mediated Metabolism of the Common Dietary Flavonoid, Quercetin

被引:37
作者
Wright, Bernice [1 ]
Gibson, Trevor [2 ]
Spencer, Jeremy [3 ]
Lovegrove, Julie A. [3 ]
Gibbins, Jonathan M. [1 ,4 ]
机构
[1] Univ Reading, Sch Biol Sci, Inst Cardiovasc & Metab Res, Reading, Berks, England
[2] Univ Reading, Bioctr Facil, Reading, Berks, England
[3] Univ Reading, Sch Food & Nutr Sci, Reading, Berks, England
[4] King Saud Univ, Blood Transfus Res Grp, Riyadh, Saudi Arabia
来源
PLOS ONE | 2010年 / 5卷 / 03期
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
O-METHYLTRANSFERASE ACTIVITY; ESSENTIAL COMPONENTS; ACTIVATION PATHWAY; SMALL-INTESTINE; IDENTIFICATION; INGESTION; RAT; BIOAVAILABILITY; PROCYANIDINS; FLAVAN-3-OLS;
D O I
10.1371/journal.pone.0009673
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Flavonoid metabolites remain in blood for periods of time potentially long enough to allow interactions with cellular components of this tissue. It is well-established that flavonoids are metabolised within the intestine and liver into methylated, sulphated and glucuronidated counterparts, which inhibit platelet function. Methodology/Principal Findings: We demonstrate evidence suggesting platelets which contain metabolic enzymes, as an alternative location for flavonoid metabolism. Quercetin and a plasma metabolite of this compound, 4'-O-methyl quercetin (tamarixetin) were shown to gain access to the cytosolic compartment of platelets, using confocal microscopy. High performance liquid chromatography (HPLC) and mass spectrometry (MS) showed that quercetin was transformed into a compound with a mass identical to tamarixetin, suggesting that the flavonoid was methylated by catechol-O-methyl transferase (COMT) within platelets. Conclusions/Significance: Platelets potentially mediate a third phase of flavonoid metabolism, which may impact on the regulation of the function of these cells by metabolites of these dietary compounds.
引用
收藏
页数:6
相关论文
共 33 条
[1]   Part of quercetin absorbed in the small intestine is conjugated and further secreted in the intestinal lumen [J].
Crespy, V ;
Morand, C ;
Manach, C ;
Besson, C ;
Demigne, C ;
Remesy, C .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 277 (01) :G120-G126
[2]   Human metabolism of dietary flavonoids: Identification of plasma metabolites of quercetin [J].
Day, AJ ;
Mellon, F ;
Barron, D ;
Sarrazin, G ;
Morgan, MRA ;
Williamson, G .
FREE RADICAL RESEARCH, 2001, 35 (06) :941-952
[3]  
DELUCA G, 1976, ITAL J BIOCHEM, V25, P213
[4]   Investigation of a correlation between monoamine oxidase B and catechol-O-methyltransferase activity in human blood cells [J].
Dingemanse, J ;
Zürcher, G ;
Kettler, R .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2000, 12 (02) :159-163
[5]   Catechin is metabolized by both the small intestine and liver of rats [J].
Donovan, JL ;
Crespy, V ;
Manach, C ;
Morand, C ;
Besson, C ;
Scalbert, A ;
Rémésy, C .
JOURNAL OF NUTRITION, 2001, 131 (06) :1753-1757
[6]   Dietary flavonoids as intracellular substrates for an erythrocyte trans-plasma membrane oxidoreductase activity [J].
Fiorani, M ;
Accorsi, A .
BRITISH JOURNAL OF NUTRITION, 2005, 94 (03) :338-345
[7]   Intracellular flavonoids as electron donors for extracellular ferricyanide reduction in human erythrocytes [J].
Fiorani, M ;
De Sanctis, R ;
De Bellis, R ;
Dachà, M .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (01) :64-72
[8]  
Frame LT, 2000, DRUG METAB DISPOS, V28, P1063
[9]   Tyrosine phosphorylation of the Fc receptor gamma-chain in collagen-stimulated platelets [J].
Gibbins, J ;
Asselin, J ;
Farndale, R ;
Barnes, M ;
Law, CL ;
Watson, SP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (30) :18095-18099
[10]   Platelet adhesion signalling and the regulation of thrombus formation [J].
Gibbins, JM .
JOURNAL OF CELL SCIENCE, 2004, 117 (16) :3415-3425