Preventive effect of epicatechin and ginsenoside Rb2 on the inhibition of gap junctional intercellular communication by TPA and H2O2

被引:97
作者
Kang, KS
Kang, BC
Lee, BJ
Che, JH
Li, GX
Trosko, JE
Lee, YS
机构
[1] Seoul Natl Univ, Coll Vet Med, Dept Vet Publ Hlth, Suwon 441744, South Korea
[2] Michigan State Univ, Natl Food Safety & Toxicol Ctr, Dept Pediat & Human Dev, E Lansing, MI 48824 USA
关键词
green tea; ginseng; catechins; ginsenosides; gap junctional intercellular communication; connexin; 43;
D O I
10.1016/S0304-3835(99)00438-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The anticarcinogenic effects of epicatechin (EC) and ginsenoside Rb-2 (Rb-2), which are major components of green tea and Korea ginseng, respectively, were investigated using a model system of gap junctional intercellular communication (GJIC) in WB-F344 rat liver epithelial cells. 12-O-tetradecanoylphorbol-13-acetate (TPA) and hydrogen peroxide, known as cancer promoters, inhibited GJIC in the epithelial cells as determined by the scrape loading/dye transfer assay, fluorescence redistribution assay after photobleaching, and immunofluorescent staining of connexin 43 using a laser confocal microscope. The inhibition of GJIC by TPA and H2O2 was prevented with treatment of Rbl or EC. The effect of EC on GJIC was stronger in TPA-treated cells than in H2O2-treated cells, while the effect of Rb-2 was opposite to that of EC. EC, at the concentration of 27.8 mug/ml, prevented the TPA-induced GJIC inhibition by about 60%. Rb-2 at the concentration of 277 mug/ml, recovered the H2O2-induced GJIC inhibition by about 60%. These results suggest that Rb-2 and EC may prevent human cancers by preventing the down-regulation of GJIC during the cancer promotion phase and that the anticancer effect of green tea and Korea ginseng may come from the major respective components, EC and Rb-2. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:97 / 106
页数:10
相关论文
共 35 条
[1]
Consumption of green tea causes rapid increase in plasma antioxidant power in humans [J].
Benzie, IFF ;
Szeto, YT ;
Strain, JJ ;
Tomlinson, B .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1999, 34 (01) :83-87
[2]
BERTHOUD VM, 1993, EUR J CELL BIOL, V62, P384
[3]
TOXICITY DETERMINED INVITRO BY MORPHOLOGICAL ALTERATIONS AND NEUTRAL RED ABSORPTION [J].
BORENFREUND, E ;
PUERNER, JA .
TOXICOLOGY LETTERS, 1985, 24 (2-3) :119-124
[4]
Green tea and cancer in humans: A review of the literature [J].
Bushman, JL .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1998, 31 (03) :151-159
[5]
PROOXIDANT STATES AND TUMOR PROMOTION [J].
CERUTTI, PA .
SCIENCE, 1985, 227 (4685) :375-381
[6]
Cancer chemopreventive and therapeutic activities of red ginseng [J].
Chen, XG ;
Liu, HY ;
Lei, XH ;
Fu, ZD ;
Li, Y ;
Tao, LH ;
Han, R .
JOURNAL OF ETHNOPHARMACOLOGY, 1998, 60 (01) :71-78
[7]
Ginsenoside-Rg1 down-regulates glucocorticoid receptor and displays synergistic effects with cAMP [J].
Chung, E ;
Lee, KY ;
Lee, YJ ;
Lee, YH ;
Lee, SK .
STEROIDS, 1998, 63 (7-8) :421-424
[8]
SCRAPE-LOADING AND DYE TRANSFER - A RAPID AND SIMPLE TECHNIQUE TO STUDY GAP JUNCTIONAL INTERCELLULAR COMMUNICATION [J].
ELFOULY, MH ;
TROSKO, JE ;
CHANG, CC .
EXPERIMENTAL CELL RESEARCH, 1987, 168 (02) :422-430
[9]
IN-VITRO GROWTH-INHIBITION OF NEOPLASTICALLY TRANSFORMED-CELLS BY NONTRANSFORMED CELLS - REQUIREMENT FOR GAP JUNCTIONAL INTERCELLULAR COMMUNICATION [J].
ESINDUY, CB ;
CHANG, CC ;
TROSKO, JE ;
RUCH, RJ .
CARCINOGENESIS, 1995, 16 (04) :915-921
[10]
Mechanistic findings of green tea as cancer preventive for humans [J].
Fujiki, H ;
Suganuma, M ;
Okabe, S ;
Sueoka, E ;
Suga, K ;
Imai, K ;
Nakachi, K ;
Kimura, S .
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1999, 220 (04) :225-228