Effect of dietary flavonoids on pathways involved in drug metabolism

被引:68
作者
Cermak, Rainer [1 ]
机构
[1] Univ Leipzig, Inst Vet Physiol, D-04103 Leipzig, Germany
关键词
drug transporters; flavonoids; phase I metabolism; phase II metabolism;
D O I
10.1517/17425255.4.1.17
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Flavonoids are a large group of plant polyphenols with presumed beneficial effects on several common diseases. The use of dietary supplements enriched with flavonoids is becoming increasingly popular. These polyphenols are substrates of enzymes like cytochrome P450 monooxygenases and phase 11 conjugation enzymes, as well as of drug transporters involved in drug excretion. Thus, they share the same metabolic pathways with many therapeutic drugs. A number of studies have demonstrated inhibition of various cytochrome P450 monooxygenases and drug transporters by flavonoids. Flavonoid-induced effects on drug bioavailability were also shown. This raises concerns about the safe use of flavonoid supplements and flavonoid-containing remedies which are not subject to legal regulations. The challenge is to find a suitable way to predict harmful drug-flavonoid interactions.
引用
收藏
页码:17 / 35
页数:19
相关论文
共 152 条
[1]   Inhibitory effect of naringin on the micronuclei induced by ifosfamide in mouse, and evaluation of its modulatory effect on the Cyp3a subfamily [J].
Alvarez-González, I ;
Madrigal-Bujaidar, E ;
Dorado, V ;
Espinosa-Aguirre, JJ .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 480 :171-178
[2]   Soy induces phase II enzymes but does not inhibit dimethylbenz[a]anthracene-induced carcinogenesis in female rats [J].
Appelt, LC ;
Reicks, MM .
JOURNAL OF NUTRITION, 1999, 129 (10) :1820-1826
[3]   Quercetin derivatives are deconjugated and converted to hydroxyphenylacetic acids but not methylated by human fecal flora in vitro [J].
Aura, AM ;
O'Leary, KA ;
Williamson, G ;
Ojala, M ;
Bailey, M ;
Puupponen-Pimiä, R ;
Nuutila, AM ;
Oksman-Caldentey, KM ;
Poutanen, K .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2002, 50 (06) :1725-1730
[4]   Lack of correlation between in vitro and in vivo studies on the effects of tangeretin and tangerine juice on midazolam hydroxylation [J].
Backman, JT ;
Mäenpää, J ;
Belle, DJ ;
Wrighton, SA ;
Kivistö, KT ;
Neuvonen, PJ .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 67 (04) :382-390
[5]   Naringin is a major and selective clinical inhibitor of organic anion-transporting polypeptide 1A2 (OATP1A2) in grapefruit juice [J].
Bailey, D. G. ;
Dresser, G. K. ;
Leake, B. F. ;
Kim, R. B. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 81 (04) :495-502
[6]   Transformation of flavonoids by intestinal microorganisms [J].
Blaut, M ;
Schoefer, L ;
Braune, A .
INTERNATIONAL JOURNAL FOR VITAMIN AND NUTRITION RESEARCH, 2003, 73 (02) :79-87
[7]   Coordinate induction by antioxidants of UDP-glucuronosyltransferase UGT1A6 and the apical conjugate export pump MRP2 (multidrug resistance protein 2) in Caco-2 cells [J].
Bock, KW ;
Eckle, T ;
Ouzzine, M ;
Fournel-Gigleux, S .
BIOCHEMICAL PHARMACOLOGY, 2000, 59 (05) :467-470
[8]   Regioselectivity of phase 11 metabolism of luteolin and quercetin by UDP-glucuronosyl transferases [J].
Boersma, MG ;
van der Woude, H ;
Bogaards, J ;
Boeren, S ;
Vervoort, J ;
Cnubben, NHP ;
van Iersel, MLPS ;
van Bladeren, PJ ;
Rietjens, IMCM .
CHEMICAL RESEARCH IN TOXICOLOGY, 2002, 15 (05) :662-670
[9]   The role of chrysin and the Ah receptor in induction of the human UGT1A1 gene in vitro and in Transgenic UGT1 mice [J].
Bonzo, Jessica A. ;
Belanger, Alain ;
Tukey, Robert H. .
HEPATOLOGY, 2007, 45 (02) :349-360
[10]   Genetic polymorphisms of drug-metabolising enzymes and drug transporters in the chemotherapeutic treatment of cancer [J].
Bosch, TM ;
Meijerman, I ;
Beijnen, JH ;
Schellens, JHM .
CLINICAL PHARMACOKINETICS, 2006, 45 (03) :253-285