Back to Search Start Over

Quercetin Significantly Inhibits the Metabolism of Caffeine, a Substrate of Cytochrome P450 1A2 Unrelated to CYP1A2*1C (-2964G>A) and *1F (734C>A) Gene Polymorphisms.

Authors :
Jian Xiao
Wei-Hua Huang
Jing-Bo Peng
Zhi-Rong Tan
Dong-Sheng Ou-Yang
Dong-Li Hu
Wei Zhang
Yao Chen
Source :
BioMed Research International; 2014, Vol. 2014, p1-6, 6p
Publication Year :
2014

Abstract

Background. Quercetin is abundant in plants and human diets. Previous studies indicated that quercetin inhibited the activity of CYP1A2, and the combination of quercetin with the substrates of CYP1A2 might produce herb-drug interactions. This research aims to determine the effects of quercetin and the CYP1A2 gene polymorphisms, namely, CYP1A2 *1C (-2964G>A) and *1F (734C>A), on the metabolism of caffeine. Method. The experiment was designed into two treatment phases separated by a 2-week washout period. Six homozygous individuals for the CYP1A2 *1C/ *1F (GG/AA) genotype and 6 heterozygous individuals for the CYP1A2 *1C/ *1F (GA/CA) genotype were enrolled in the study. Quercetin capsules (500mg) were given to each volunteer once daily for 13 consecutive days, and after that, each subject was coadministrated 100 mg caffeine capsules with 500mg quercetin on the 14th day. Then a series of venous blood samples were collected for HPLC analysis. Correlation was determined between pharmacokinetics of caffeine and paraxanthine with caffeine metabolite ratio. Results. Quercetin significantly affected the pharmacokinetics of caffeine and its main metabolite paraxanthine, while no differences were found in the pharmacokinetics of caffeine and paraxanthine between GG/AA and GA/CA genotype groups. Conclusion. Quercetin significantly inhibits the caffeine metabolism, which is unrelated to CYP1A2 *1C (-2964G>A) and *1F (734C>A) gene polymorphisms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23146133
Volume :
2014
Database :
Complementary Index
Journal :
BioMed Research International
Publication Type :
Academic Journal
Accession number :
100579023
Full Text :
https://doi.org/10.1155/2014/405071