Interaction between the aryl hydrocarbon receptor and its antagonists, flavonoids

被引:43
作者
Fukuda, Itsuko
Mukai, Rie
Kawase, Masaya
Yoshida, Ken-ichi
Ashida, Hitoshi
机构
[1] Kobe Univ, Grad Sch Agr Sci, Res Ctr Food Safety & Secur, Kobe, Hyogo 6578501, Japan
[2] Kobe Univ, Grad Sch Agr Sci, Dept Agrobiosci, Kobe, Hyogo 6578501, Japan
[3] Osaka Ohtani Univ, Fac Pharmaceut Sci, Osaka, Japan
基金
日本学术振兴会;
关键词
aryl hydrocarbon receptor; flavonoid; flavone; galangin; eriodictyol; (-)-epigallocatechin gallate; sensor plasmon resonance (SPR) analysis;
D O I
10.1016/j.bbrc.2007.05.199
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 have been reported to be dietary antagonists of an aryl hydrocarbon receptor (AhR). However, little is known about the molecular mechanism on their antagonistic effects. In this study, the inhibitory effect of flavonoids on ligand binding to the AhR and interaction between flavonoids and the AhR complex (AhRc) were investigated in each flavonoid subclass. Flavone, flavonol, and flavanone but not catechin inhibited the specific binding between the AhR and 3-methylcholanthrene dose-dependently, indicating that the former three subclasses possibly act as competitive antagonists of the AhR. However, catechin in addition to the former three subclasses directly interacted with the AhRc by surface plasmon resonance analysis. The dissociation constant values showed an inverse correlation with the suppressive effect on the DNA binding activity. These results suggest that flavone, flavonol, and flavanone act as competitive antagonists of the AhR, while catechin associates with the AhRc and indirectly exhibits its antagonistic effects. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:822 / 827
页数:6
相关论文
共 25 条
[1]   Screening of the inhibitory effect of vegetable constituents on the aryl hydrocarbon receptor-mediated activity induced by 2.3,7,8-tetrachlorodibenzo-p-dioxin [J].
Amakura, Y ;
Tsutsumi, T ;
Sasaki, K ;
Yoshida, T ;
Maitani, T .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2003, 26 (12) :1754-1760
[2]   Flavones and flavonols at dietary levels inhibit a transformation of aryl hydrocarbon receptor induced by dioxin [J].
Ashida, H ;
Fukuda, I ;
Yamashita, T ;
Kanazawa, K .
FEBS LETTERS, 2000, 476 (03) :213-217
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Dietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentially [J].
Ciolino, HP ;
Daschner, PJ ;
Yeh, GC .
BIOCHEMICAL JOURNAL, 1999, 340 :715-722
[5]  
Ciolino HP, 1999, MOL PHARMACOL, V56, P760
[6]   Effect of curcumin on the aryl hydrocarbon receptor and cytochrome P450 1A1 in MCF-7 human breast carcinoma cells [J].
Ciolino, HP ;
Daschner, PJ ;
Wang, TTY ;
Yeh, GC .
BIOCHEMICAL PHARMACOLOGY, 1998, 56 (02) :197-206
[7]  
Denison MS, 1998, TARG ORG T, P3
[8]   Ligand binding and activation of the Ah receptor [J].
Denison, MS ;
Pandini, A ;
Nagy, SR ;
Baldwin, EP ;
Bonati, L .
CHEMICO-BIOLOGICAL INTERACTIONS, 2002, 141 (1-2) :3-24
[9]   Pigments in green tea leaves (Camellia sinensis) suppress transformation of the aryl hydrocarbon receptor induced by dioxin [J].
Fukuda, I ;
Sakane, I ;
Yabushita, Y ;
Kodoi, R ;
Nishiumi, S ;
Kakuda, T ;
Sawamura, SI ;
Kanazawa, K ;
Ashida, H .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (09) :2499-2506
[10]   THE EXAMINATION AND QUANTITATION OF TISSUE CYTOSOLIC RECEPTORS FOR 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN USING HYDROXYLAPATITE [J].
GASIEWICZ, TA ;
NEAL, RA .
ANALYTICAL BIOCHEMISTRY, 1982, 124 (01) :1-11