Flavonoids-potent and versatile biologically active compounds interacting with cytochromes P450

被引:479
作者
Hodek, P
Trefil, P
Stiborová, M
机构
[1] Charles Univ Prague, Dept Biochem, CZ-12840 Prague, Czech Republic
[2] Biopharm, Res Inst Biopharm & Vet Drugs, CZ-25449 Jilove, Czech Republic
关键词
flavonoids; cytochrome P450; induction; inhibition; aromatase; cancer;
D O I
10.1016/S0009-2797(01)00285-X
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 represent a group of phytochemicals exhibiting a wide range of biological activities arising mainly from their antioxidant properties and ability to modulate several enzymes or cell receptors. Flavonoids have been recognized to exert anti-bacterial and anti-viral activity, anti-inflammatory, anti-angionic, analgesic, anti-allergic effects, hepatoprotective, cytostatic, apoptotic, estrogenic and anti-estrogenic properties. However, not all flavonoids and their actions are necessarily beneficial. Some flavonoids have mutagenic and/or prooxidant effects and can also interfere with essential biochemical pathways. Among the proteins that interact with flavonoids, cytochromes P450 (CYPs), monooxygenases metabolizing xenobiotics (e.g. drugs, carcinogens) and endogenous substrates (e.g. steroids), play a prominent role. Flavonoid compounds influence these enzymes in several ways: flavonoids induce the expression of several CYPs and modulate (inhibit or stimulate) their metabolic activity. In addition, some CYPs participate in metabolism of flavonoids. Flavonoids enhance activation of carcinogens and/or influence the metabolism of drugs via induction of specific CYPs, On the other hand, inhibition of CYPs involved in carcinogen activation and scavenging reactive species formed from carcinogens by CYP-mediated reactions can be beneficial properties of various flavonoids. Flavonoids show an estrogenic or anti-estrogenic activity owing to the Structural similarity with the estrogen skeleton. Mimicking natural estrogens, they bind to estrogen receptor and modulate its activity. They also block CYP19, a crucial enzyme involved in estrogen biosynthesis. Flavonoids ill human diet may reduce the risk of various cancers, especially hormone-dependent breast and prostate cancers. as well preventing menopausal symptoms. For these reasons the structure-function relationship of flavonoids is extensively studied to provide an inspiration for a rational drug and/or chemopreventive agent design Of future pharmaceuticals. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 21
页数:21
相关论文
共 96 条
[41]   Inhibition of aromatase activity by flavonoids [J].
Jeong, HJ ;
Shin, YG ;
Kim, IH ;
Pezzuto, JM .
ARCHIVES OF PHARMACAL RESEARCH, 1999, 22 (03) :309-312
[42]   Quercetin inhibits benzo[a]pyrene-induced DNA adducts in human Hep G2 cells by altering cytochrome P-450 1A1 gene expression [J].
Kang, ZC ;
Tsai, SJ ;
Lee, H .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 35 (02) :175-179
[43]   Molecular basis of the inhibition of human aromatase (estrogen synthetase) by flavone and isoflavone phytoestrogens: A site-directed mutagenesis study [J].
Kao, YC ;
Zhou, CB ;
Sherman, M ;
Laughton, CA ;
Chen, S .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1998, 106 (02) :85-92
[44]   INHIBITION OF HUMAN ESTROGEN SYNTHETASE (AROMATASE) BY FLAVONES [J].
KELLIS, JT ;
VICKERY, LE .
SCIENCE, 1984, 225 (4666) :1032-1034
[45]   INHIBITION OF AROMATASE CYTOCHROME-P-450 (ESTROGEN SYNTHETASE) BY DERIVATIVES OF ALPHA-NAPHTHOFLAVONE [J].
KELLIS, JT ;
NESNOW, S ;
VICKERY, LE .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (17) :2887-2891
[46]   Flavonoids suppress androgen-independent human prostate tumor proliferation [J].
Knowles, LM ;
Zigrossi, DA ;
Tauber, RA ;
Hightower, C ;
Milner, JA .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2000, 38 (01) :116-122
[47]   Physiological modeling of a proposed mechanism of enzyme induction by TCDD [J].
Kohn, MC ;
Walker, NJ ;
Kim, AH ;
Portier, CJ .
TOXICOLOGY, 2001, 162 (03) :193-208
[48]   Estrogenic effects of silymarin in ovariectomized rats [J].
Kummer, V ;
Masková, J ;
Canderle, J ;
Zraly, Z ;
Neca, J ;
Machala, M .
VETERINARNI MEDICINA, 2001, 46 (01) :17-23
[49]   Structure-related inhibition of human hepatic caffeine N3-demethylation by naturally occurring flavonoids [J].
Lee, H ;
Yeom, H ;
Kim, YG ;
Yoon, CN ;
Jin, CB ;
Choi, JS ;
Kim, BR ;
Kim, DH .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (09) :1369-1375
[50]   Grapefruit juice and its flavonoids inhibit 11 beta-hydroxysteroid dehydrogenase [J].
Lee, YS ;
Lorenzo, BJ ;
Koufis, T ;
Reidenberg, MM .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 59 (01) :62-71