Effect of commercially available green and black tea beverages on drug-metabolizing enzymes and oxidative stress in Wistar rats

被引:22
作者
Yao, Hsien-Tsung [1 ]
Hsu, Ya-Ru [1 ]
Lii, Chong-Kuei [1 ,2 ]
Lin, Ai-Hsuan [1 ]
Chang, Keng-Hao [1 ]
Yang, Hui-Ting [1 ]
机构
[1] China Med Univ, Dept Nutr, Taichung 404, Taiwan
[2] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung 413, Taiwan
关键词
Green tea; Black tea; Drug-metabolizing enzymes; Oxidative stress; Rats; PHASE-II ENZYMES; INDUCTION; POLYPHENOLS; LIVER; TRANSFORMATION; GLUTATHIONE; INHIBITION; RECEPTOR; CYSTEINE; INFLAMMATION;
D O I
10.1016/j.fct.2014.04.043
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The effect of commercially available green tea (GT) and black tea (BT) drinks on drugmetabolizing enzymes (DME) and oxidative stress in rats was investigated. Male Wistar rats were fed a laboratory chow diet and GT or BT drink for 5 weeks. Control rats received de-ionized water instead of the tea drinks. Rats received the GT and BT drinks treatment for 5 weeks showed a significant increase in hepatic microsomal cytochrome P450 (CYP) 1A1 and CYP1A2, and a significant decrease in CYP2C, CYP2E1 and CYP3A enzyme activities. Results of immunoblot analyses of enzyme protein contents showed the same trend with enzyme activity. Significant increase in UDP-glucuronosyltransferase activity and reduced glutathione content in liver and lungs were observed in rats treated with both tea drinks. A lower lipid peroxide level in lungs was observed in rats treated with GT drink. Electrophoretic mobility shift assay revealed that both tea drinks decreased pregnane X receptor binding to DNA and increased nuclear factor-erythroid 2 p45-related factor 2 binding to DNA. These results suggest that feeding of both tea drinks to rats modulated DME activities and reduced oxidative stress in liver and lungs. GT drink is more effective on reducing oxidative stress than BT drink. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:120 / 127
页数:8
相关论文
共 54 条
  • [1] Emerging role of Nrf2 in protecting against hepatic and gastrointestinal disease
    Aleksunes, Lauren M.
    Manautou, Jose E.
    [J]. TOXICOLOGIC PATHOLOGY, 2007, 35 (04) : 459 - 473
  • [2] ALI SF, 1992, NEUROTOXICOLOGY, V13, P637
  • [3] The aryl hydrocarbon receptor complex and the control of gene expression
    Beischlag, Timothy V.
    Morales, J. Luis
    Hollingshead, Brett D.
    Perdew, Gary H.
    [J]. CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2008, 18 (03): : 207 - 250
  • [4] BuAbbas A, 1997, J SCI FOOD AGR, V75, P453, DOI 10.1002/(SICI)1097-0010(199712)75:4<453::AID-JSFA897>3.0.CO
  • [5] 2-3
  • [6] Human and Rat Primary Hepatocyte CYP1A1 and 1A2 Induction with 2,3,7,8-Tetrachlorodibenzo-p-dioxin, 2,3,7,8-Tetrachlorodibenzofuran, and 2,3,4,7,8-Pentachlorodibenzofuran
    Budinsky, Robert A.
    LeCluyse, Edward L.
    Ferguson, Stephen S.
    Rowlands, J. Craig
    Simon, Ted
    [J]. TOXICOLOGICAL SCIENCES, 2010, 118 (01) : 224 - 235
  • [7] SENSITIVE ENZYMATIC METHOD FOR DETERMINATION OF FREE AND ESTERIFIED TISSUE CHOLESTEROL
    CARLSON, SE
    GOLDFARB, S
    [J]. CLINICA CHIMICA ACTA, 1977, 79 (03) : 575 - 582
  • [8] Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
    Chen, Haw-Wen
    Huang, Chin-Shiu
    Liu, Pei-Fen
    Li, Chien-Chun
    Chen, Chiung-Tong
    Liu, Cheng-Tzu
    Chiang, Jia-Rong
    Yao, Hsien-Tsung
    Lii, Chong-Kuei
    [J]. EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2013, 2013
  • [9] Chen LS, 1996, DRUG METAB DISPOS, V24, P529
  • [10] Protective effect of tea polyphenols against paracetamol-induced hepatotoxicity in mice is significanly correlated with cytochrome P450 suppression
    Chen, Xia
    Sun, Chang-Kai
    Han, Guo-Zhu
    Peng, Jin-Yong
    Li, Ying
    Liu, Yan-Xia
    Lv, Yuan-Yuan
    Liu, Ke-Xin
    Zhou, Qin
    Sun, Hui-Jun
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (15) : 1829 - 1835