Tea polyphenols inhibit the transport of dietary phenolic acids mediated by the monocarboxylic acid transporter (MCT) in intestinal Caco-2 cell monolayers

被引:67
作者
Konishi, Y
Kobayashi, S
Shimizu, M
机构
[1] Kirin Brewery Co Ltd, Appl Biores Ctr, Dept Res & Dev, Takasaki, Gumma 3701295, Japan
[2] Takasaki Univ Hlth & Welf, Dept Food & Life Sci, Takasaki, Gumma 3700033, Japan
[3] Univ Tokyo, Dept Appl Biol Chem, Grad Sch Agr & Life Sci, Bunkyo Ku, Tokyo 1138657, Japan
关键词
tea polyphenols; catechins; monocarboxylic acid transporter; fluorescein; Caco-2;
D O I
10.1021/jf034894t
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
It was previously reported that a fluorescent marker dye, fluorescein, is transported via the monocarboxylic acid transporter (MCT). Fluorescein transport was competitively inhibited by MCT substrates such as ferulic and salicylic acids. Tea polyphenols, in particular, epigallocatechin gallate (EGCg) and epicatechin gallate (ECg), inhibited the transport of fluorescein. Tea polyphenols also inhibited the transport of salicylic and ferulic acids, suggesting tea polyphenols might be substrates of MCT. However, the transepithelial flux of tea polyphenols was much lower than that of the MCT substrates and was inversely correlated with the paracellular permeability of Caco-2 cell monolayers. These findings suggest that tea polyphenols are not substrates but inhibitors of MCT. Furthermore, the transepithelial transport of these polyphenols is mainly via paracellular diffusion. However, directional transport of ECg and EGCg from the basolateral to the apical side was observed, indicating that the behavior of tea polyphenols in the intestinal epithelium is complex.
引用
收藏
页码:7296 / 7302
页数:7
相关论文
共 30 条
[1]   CORRELATION BETWEEN ORAL-DRUG ABSORPTION IN HUMANS AND APPARENT DRUG PERMEABILITY COEFFICIENTS IN HUMAN INTESTINAL EPITHELIAL (CACO-2) CELLS [J].
ARTURSSON, P ;
KARLSSON, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (03) :880-885
[2]   Characterization of the high-affinity monocarboxylate transporter MCT2 in Xenopus laevis oocytes [J].
Bröer, S ;
Bröer, A ;
Schneider, HP ;
Stegen, C ;
Halestrap, AP ;
Deitmer, JW .
BIOCHEMICAL JOURNAL, 1999, 341 :529-535
[3]   High-performance liquid chromatography coupled with coulometric array detection of electroactive components in fruits and vegetables: Relationship to oxygen radical absorbance capacity [J].
Guo, CJ ;
Cao, GH ;
Sofic, E ;
Prior, RL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (05) :1787-1796
[4]   The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation [J].
Halestrap, AP ;
Price, NT .
BIOCHEMICAL JOURNAL, 1999, 343 :281-299
[5]   Interaction of tea catechins with lipid bilayers investigated with liposome systems [J].
Hashimoto, T ;
Kumazawa, S ;
Nanjo, F ;
Hara, Y ;
Nakayama, T .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1999, 63 (12) :2252-2255
[6]   REDUCTION OF CHRONIC PSYCHOSOCIAL HYPERTENSION IN MICE BY DECAFFEINATED TEA [J].
HENRY, JP ;
STEPHENSLARSON, P .
HYPERTENSION, 1984, 6 (03) :437-444
[7]  
HIDALGO IJ, 1989, GASTROENTEROLOGY, V96, P736
[8]   CACO-2 CELL MONOLAYERS AS A MODEL FOR DRUG TRANSPORT ACROSS THE INTESTINAL-MUCOSA [J].
HILGERS, AR ;
CONRADI, RA ;
BURTON, PS .
PHARMACEUTICAL RESEARCH, 1990, 7 (09) :902-910
[9]   INHIBITION OF RAT SMALL INTESTINAL SUCRASE AND ALPHA-GLUCOSIDASE ACTIVITIES BY TEA POLYPHENOLS [J].
HONDA, M ;
HARA, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1993, 57 (01) :123-124
[10]  
Hong J, 2002, CANCER RES, V62, P7241