Green tea polyphenol epigallocatechin-3-gallate differentially modulates oxidative stress in PC12 cell compartments

被引:95
作者
Raza, H [1 ]
John, A [1 ]
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Biochem, Al Ain, U Arab Emirates
关键词
tea polyphenol -EGCG; PC12; cells; GSH metabolism; oxidative stress; apoptosis;
D O I
10.1016/j.taap.2005.01.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tea polyphenols have been reported to be potent antioxidants and beneficial in oxidative stress related diseases. Prooxidant effects of tea polyphenols have also been reported in cell culture systems. In the present study, we have studied oxidative stress in the subcellular compartments of PC 12 cells after treatment with different concentrations of the green tea polyphenol, epigallocatechin-3-gallate (EGCG). We have demonstrated that EGCG has differentially affected the production of reactive oxygen species (ROS), glutathione (GSH) metabolism and cytochrome P450 2E1 activity in the different subcellular compartments in PC12 cells. Our results have shown that although the cell survival was not inhibited by EGCG, there was, however, an increased DNA breakdown and activation of apoptotic markers, caspase 3 and poly-(ADP-ribose) polymerase (PARP) at higher concentrations of EGCG treatment. Our results suggest that the differential effects of EGCG might be related to the alterations in oxidative stress, GSH pools and CYP2E1 activity in different cellular compartments. These results may have implications in determining the chemopreventive therapeutic use of tea polyphenols in vivo. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:212 / 220
页数:9
相关论文
共 40 条
[1]   Oral consumption of green tea polyphenols inhibits insulin-like growth factor-i-induced signaling in an autochthonous mouse model of prostate cancer [J].
Adhami, VM ;
Siddiqui, IA ;
Ahmad, N ;
Gupta, S ;
Mukhtar, H .
CANCER RESEARCH, 2004, 64 (23) :8715-8722
[2]   Cell cycle dysregulation by green tea polyphenol epigallocatechin-3-gallate [J].
Ahmad, N ;
Cheng, PY ;
Mukhtar, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 275 (02) :328-334
[3]   Green tea constituent epigallocatechin-3-gallate and induction of apoptosis and cell cycle arrest in human carcinoma cells [J].
Ahmad, N ;
Feyes, DK ;
Nieminen, AL ;
Agarwal, R ;
Mukhtar, H .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (24) :1881-1886
[4]   Differential modulation of growth and glutathione metabolism in cultured rat astrocytes by 4-hydroxynonenal and green tea polyphenol, epigallocatechin-3-gallate [J].
Ahmed, I ;
John, A ;
Vijayasarathy, C ;
Robin, MA ;
Raza, H .
NEUROTOXICOLOGY, 2002, 23 (03) :289-300
[5]   Oxidative stress, toxicology, and pharmacology of CYP2E1 [J].
Caro, AA ;
Cederbaum, AI .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2004, 44 :27-42
[6]   Contribution of hydrogen peroxide to the cytotoxicity of green tea and red wines [J].
Chai, PC ;
Long, LH ;
Halliwell, B .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (04) :650-654
[7]   Specific induction of glutathione S-transferase GSTM2 subunit expression by epigallocatechin gallate in rat liver [J].
Chou, FP ;
Chu, YC ;
Hsu, JD ;
Chiang, HC ;
Wang, CJ .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (05) :643-650
[8]   Dual mechanisms of green tea extract-induced cell survival in human epidermal keratinocytes [J].
Chung, JH ;
Han, JH ;
Hwang, EJ ;
Seo, JY ;
Cho, KH ;
Kim, KH ;
Youn, JI ;
Eun, HC .
FASEB JOURNAL, 2003, 17 (11) :1913-+
[9]   A review of latest research findings on the health promotion properties of tea [J].
Dufresne, CJ ;
Farnworth, ER .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2001, 12 (07) :404-421
[10]   A SELECTIVE PROCEDURE FOR DNA EXTRACTION FROM APOPTOTIC CELLS APPLICABLE FOR GEL-ELECTROPHORESIS AND FLOW-CYTOMETRY [J].
GONG, JP ;
TRAGANOS, F ;
DARZYNKIEWICZ, Z .
ANALYTICAL BIOCHEMISTRY, 1994, 218 (02) :314-319