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研究生:王志偉
研究生(外文):David Ong
論文名稱:茶葉兒茶素之生理活性
論文名稱(外文):The Physiological Activities of Tea Catechins
指導教授:蔡國珍
學位類別:碩士
校院名稱:國立臺灣海洋大學
系所名稱:食品科學系
學門:農業科學學門
學類:食品科學類
論文種類:學術論文
論文出版年:2005
畢業學年度:93
語文別:中文
論文頁數:109
中文關鍵詞:兒茶素
外文關鍵詞:Catechins
相關次數:
  • 被引用被引用:17
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中文摘要

本文主要探討茶葉多元酚中的主要成份-兒茶素的生理活性,尤其是抗氧化、抗菌與抗腫瘤活性。
兒茶素清除氫氧化自由基的能力依序為epicatechin gallate(ECG)>epigallocatechin gallate(EGCG)>epicatechin(EC)>gallic acid(GA)>gallocatechin(GC)>epigallocatechin(EGC),均大於>Vit. C。其中ECG及EGCG清除超過氧化物及過氧化氫能力比維生素C及E強8.32倍。兒茶素可有效抑制低密度脂蛋白(LDL)的氧化,進而降低發生動脈硬化的機率。
EGCG抗菌活性大於EC,二者均對G(+)細菌抗菌活性大於G(-)細菌,EGCG對金黃色葡萄球菌與大腸桿菌之最低抑制濃度(MIC)分別為73與573 �慊/ml。EC對金黃色葡萄球菌與大腸桿菌之MIC為183及>1145 �慊/ml。藉由微脂粒的作用模式得知EGCG與EC對菌體作用機制乃破壞菌體細胞膜,導致內容物外漏而致菌體死亡,膜上負電荷明顯降低二者的作用活性。
兒茶素抗腫瘤效應,不管是體外或體内試驗的證據,都顯示在癌症發展的數個階段中均具有正面效應,包括癌症初始期、促成期及蔓延期、到腫瘤的轉移等。依照目前各種研究結果顯示,兒茶素可以抑制癌細胞的生長,促使癌細胞程式化死亡(aptosis),抑制腫瘤促進劑(tumor promoter)、賀爾蒙、cytokine及生長因子等的作用。兒茶素抑制癌細胞生長的主要藉由細胞循環調節(cell cycle regulation),EGCG可以提高細胞以G2-M相存在的比例,實驗結果顯示50 �嵱及100 �嵱的EGCG可以將細胞以G2-M相存在的比例,由13.8﹪分別提高到15.6﹪及24.1﹪,這種效應發現與EGCG的濃度相關。有關兒茶素抗癌及抗腫瘤效應之動物試驗的研究報告依照癌症的種類有(一)以N-nitrosodiethylamine(NDEA)注射雌性A/J鼠誘發腫瘤。(二)以N-nitrosomethylbenzylamine(NMBzA)誘發Wistar大鼠食道腫瘤。(三)以7,12-dimethylbenz[a]anthracene(DMBA)處理SENCAR老鼠,再以TPA局部處理以誘發腫瘤。(四)以N-ethyl-N’-nitro-N-nitroguanidine及azoxymethane(AOM)誘發腸癌。
Abstract

This study mainly reviews the antioxidative, antimicrobial and anticancer activities of the catechins, the dominant polyphenol components in tea. The scanvanging activity for hydroxy radical ranks in order as epicatechin gallate (ECG) >epigallocatechin gallate(EGCG)>epicatechin(EC)>gallic acid(GA)>gallocatechin(GC)>epigallocatechin(EGC), all of which are greater than that of Vit C. The scanvanging activity of ECG and EGCT for superoxide and hydrogen peroxide is greater than that of Vit C and Vit E by 8.32 times. Catechins can inhibit the oxidation of the low density lipoproteins and accordingly, decrease the risk for arteriosclerosis.
The antibacterial activity of EGCG is greater than that of EC. Both EGCG and EC have stronger effect on G(+)bacteria than G(-)bacteria. The minimal inhibition concentration(MIC)of EGCG for S. aureus.and E.coli are 73 and 573 �慊/ml, respectively, while the MIC for EC are 183 and >1145 �慊/ml, respectively. The data from the action on liposome demonstrate that both EGCG and EC can damage the cell membrane and result in the leakage of the cell. The presence of the negative residues in membrane deaease the actions of EGCG and EC on the membrane.
Catechins can inhibit the propogation of cancer cell by inducing the aptosis of cell and inhibiting the functions of tumor promoters, hormones, cytokines and growth factors. In the presence of 50 �慆 and 100 �慆 of EGCG the ratio for cells in G2-M phase was increased from 13.8﹪to 15.6﹪and 24.1﹪, respectively. The animal models used for the anticancer / antitumor study of catechins include: (1)N-nitrosodiethylamine injection to in A/J mice induce cancer production;(2)N-nitrosomethylbenzylamine induced the cancer of esophagus of Wistar rats;(3)treatments by 7,12-dimethylbenz[a]anthracene and 12-0-tetrade canoylphorbol-13-acetete to induce skin cancer in SENCAR rats; (4)induction of colon cancer in rats by N-ethyl-N’-nitro-N-nitroguanidine and azoxymethane.
目錄

中文摘要 ……………………………………………………………1
英文摘要 ……………………………………………………………3
一、 前言……………………………………………………………5
二、 茶的分類名稱、製造及保健…………………………………8
(一) 茶的分類名稱 …………………………………………8
(二) 茶葉製造及保健………………………………………10
三、 茶多元酚的分類……………………………………………..17
四、 兒茶素之機能性簡介………………………………………..19
五、 兒茶素之抗氧化作用………………………………………..21
(一)活性氧分子與自由基之清除者…………………………..21
(二)減少低密度脂蛋白(LDL)之氧化作用………………...22
六、 兒茶素之抗菌特性…….....…………………………………..25
(一)茶葉/兒茶素對微生物的作用機制………………………..25
(二)兒茶素的抗菌活性………………………………………..29
七、 兒茶素之抗腫瘤效應………………………………………..38
(一)流行病學研究……………………………………………..38
(二)實驗研究……….………………………………………….42
八、 結論…….……………………………………………………..53
九、 參考文獻……………………………………………………..83
圖目錄

圖1 全發酵茶製程圖………………………………………………55
圖2 不發酵茶製程圖………………………………………………56
圖3 半發酵茶製程圖………………………………………………57
圖4 兒茶素類多元酚的化學結構…………………………………58

表目錄

表1 以醱酵程度分類之成茶名稱…………………………………59
表2 以醱酵百分比的程度分類成茶名稱…………………………60
表3 以焙火程度分類之茶的名稱…………………………………61
表4 春茶、夏茶、秋茶、冬茶等季節名稱………………………62
表5 茶葉中保健成分及其功效簡表………………………………63
表6 兒茶素類機能性一覽表………………………………………64
表7 茶中抗氧化物對於自由基的清除效率………………………65
表8 體外實驗(in vitro)中,茶中抗氧化成份對於預防LDL
氧化反應的效果 ………………………………………………66
表9 兒茶素EC與EGCG導致CF從PC脂質體釋出的程度………67
表10 脂質成份影響兒茶素破壞脂質體釋出的CF的作用 ……68
表11 兒茶素EGCG存在的脂質體懸浮液測得NPN之相對螢光
強度…………………………………………………………69
表12不同濃度EGCG對脂質體的破壞作用………………………70
表13 EGCG對帶不同電荷之PC脂質體之破壞情形 ……………71
表14(A) 兒茶素對金黃色葡萄球菌的破壞作用…………………72
表14(B) 兒茶素對大腸桿菌的破壞作用…………………………72
表15 EGCG及EC對金黃色葡萄球菌及大腸桿菌的抗菌活性……73


表16 日本綠茶萃取液的抗菌作用 ………………………………74
表17 日本綠茶萃取液的滅菌作用 ………………………………75
表18 三種茶葉萃取液在不同濃度下對mycoplasma的作用……76
表19 紅茶與漱口水減少菌斑形成的效果 ………………………77
表20 不同濃度綠茶茶湯對NDEA(N-nitrosodiethylamine)
誘發雌性A/J鼠腫瘤之發生率與腫瘤數目之效應………78
表21 去咖啡因綠茶及紅茶茶湯對NNK誘發雌性A/J鼠
腫瘤之發生率與腫瘤數目之效應…………………………79
表22 綠茶兒茶素抑制AOM誘發腫瘤之效應……………………80
表23 EGCG抑制uPA的活性………………………………………81
表24 EGCG、EGC、ECG、EC及咖啡因對PC-9細胞吸收
[3H]EGCG之影響……………………………………………82
參考文獻

阮逸明. 1996. 茶葉多樣化產品簡介. 行政院農業委員會茶業改良場.桃園. pp. 1
行政院農業委員會茶業改良場. 2003. 茶葉保健. 行政院農業委員會.桃園. pp. 2
金洪良. 2002. 不可思議的綠茶. 林鬱事業有限公司. 台北. pp. 68-80
林瑞萱. 2001. 陸羽茶經講座. 武陵出版有限公司. 台北. pp. 57-60
林聖泰. 2004. 品香賞味中國茶. 暢文出版社. 台北. pp. 20-57
吳宗碩. 2000. 茶與生活. 協合文化. 台北. pp. 37-45
吳智和. 1985. 茶的文化. 行政院文化建設委員會. 台北. pp. 22-23
吳淑玲. 2001. 茶藝與信仰. 道聲出版社. 台北. pp. 27-69
范增平. 2002. 茶藝學. 萬卷樓. 台北. pp. 29-30
涂宗和. 2004. 台灣茶饌1. 翰林茶館出版. 台南. pp. 6-37
郭子儀. 2003. 喫茶享瘦. 二魚文化事業有限公司. 台北. pp. 6-7
郭玉梅. 1999. 吃出健康吃出美/吃茶篇. 活水文化出版社. 台北. pp. 8-9
原征彥. 1998. 茶兒茶素(Catechin)類的生理活性作用(1). In”茶葉多元酚在食品/保健食品產業之製造及應用研討會”pp.11.食品工業發展研究所. 新竹. 台灣. 中華民國.
張豐榮. 1991. 飲茶與賞壺. 冠倫文化. 台北. pp. 5-28
程竹青. 1999. 膳食與癌症. 食品工業31(5):12-31.
黃安希. 2003. 品茗、賞詩、中國茶. 三悅文化圖書事業有限公司. 台北. pp. 98-108
黃墩岩. 2002. 中國茶道. 暢文出版社. 台北. pp. 116-118
楊光玉. 羅慶芳. 1995. 中國藥茶大全. 林鬱事業有限公司. 台北. pp. 37-41. 56-72.
劉裕. 1998. 茶的保健功能與藥用便方. 浩園文化. 台北. pp. 8-12. 33-42. 44-77.
蔡英嬌. 1987. 新茶道之旅. 福利文化事業有限公司. 台北. pp. 2-3
Blot, W. J., McLaighlin, J. K., and Chow, W. –H. 1997. Cancer rates among drinkers of black tea. Critical Reviews in Food Science and Nutrition. 37:739-760.
Butler, L. G., Rogler, J. C., Mehansho, H., and Carlson. 1986. Dietary effects of tannins. In: Plant Flavonoids in Biology and Medicine: Biochemical Phannacological and Structure-Activity Relationships. pp. 141-157. Cody, V., Harbome, J. B., and Middleton, E., Eds., Alan R. Liss. New York.
Cadenas. E. 1989. Biochemistry of oxygen toxicity. Annu Rev Biochem 58:79-110
Cao. G., Sofic, E. and Prior. R.1996. Antioxidant capacity of tea and common vegetables. J Agric Food Chem 44:3426-3431
Chen, L., Lee, M. –L., Li, H. and Yang, C. S. 1997. Absorption, distribution and elimination of tea polyphenols in rats 1. Drug Metab. Dispos. 25(9):1045-1050.
Chen, Z. P., Schell, J. B., Ho, C. T., and Chen, K. Y. 1998. Green tea epigallocatechin gallate shows a pronounced growth inhibitory effect on cancerous cells but not on their normal counterparts. Cancer Lett. 129:173-179.
Das, N. P. 1971. Studies on flavonoid metabolism. Absorption and metabolism of (+)-catechin in man. Biochem. Phannacol 20:3435-3445.
Das, N. P. and Griffiths, L. A. 1969. Studies on flavonoid metabolism. Metabolism of (+)-[14C]catechin in the rat and guinea pig. Biochem. J. 115:831-836.
Das, N. P. and Sothy, S. P. 1971. Studies on flavonoid metabolism: biliary and urinary excretion 0f(+)(U-14C) catechin. Biochem. J. 125:417.
Dong, Z., Ma, W., Huang, C., and Yang, C. S. 1997. Inhibition of tumor promoter-induced activator protein 1 activation and cell transformation by tea polyphenols, (-)-epigallocatechin gallate and theaflavins. Cancer Res. 57:4414-4419.
Dreosti, I. E., Wargovich, M. J., and Yang, C. S. 1997. Inhibition of carcinogenesis by tea: The evidence from experimental studies. Critical Reviews in Food Science and Nutrition. 37(8):761-770.
Gao, Y. T., Maclaughlin, J. K., and Blot, W. J. 1994. Reduced risk of esophageal cancer associated with green tea consumption. J. Natl Cancer Inst. 86:855-858.
Griffiths, L. A. 1964. Studies on flavonoid metabolism. Identification of the metabolities of (+)-catechin in rat urine. Biochem. J.92:173-179.
Guo, Q., Zhao, B., Li, M., Shen, S., and Xin, W.1996. Studies on protective mechanisms of four components of green tea polyphenols against lipidperoxidation in synaptosomes. Biochim Biophys Acta 11304:210-222.
Hackett, A. M., Griffiths, L. H., Broillet, A., and Wermeille, M. 1983. The metabolism and excretion of (+)-[14C]cyanidanol-3 in man following oral administration. Xenobiotica 13:279-286.
Hamada, S. and Slade, H.D.1980. Biology, immunology and cariogenicity of Streptococcus mutans. Microbial Rev.44,331-384.
Hamilton-Miller,J. M. T. 1995. Antimicrobial properties of tea(Camellia sinensis L).Antimicro. Agents and Chemotherapy. 39(11):2375-2377.
Han, C., and Xu, Y. 1990. The effect of Chinese tea on the occurrence of esophageal tumors induced by N-nitrosomethylbenzylamine in rats. Biomed. Environ. Sci. 3:35.
Harada, M., Kan, Y., Naoki, H., Fukui, Y., Kageyama, N., Nakai. M., Miki, W., and Kiso, Y. 1999. Identification of the majar antioxidative metabolites in biological fluids of the rat with ingested(+)-catechin and (-)-epicatechin. Biosci. Biotechnol. Biochem. 63(6):973-977.
Hatano, T., Edmatsu, M., and Mori, A. 1989. Effects of the interaction of tannins with co-existing substances. VI. Effects of tannins and related polyphenols on superoxide anion radical and on 1, 1-diphenyl-2-prerythydrazyl radical. Chem Pharm Bull 37:2016-21.
He, Y. H. and Kies, C. 1994. Green and black tea consumption by humans: impact on polyphenol concentration in feces, blood and urine. Plant Food Hum. Nutr. 46:221-229.
Hirose. M., Hoshiya, T., Akagi, K., Takahashi, S., Hara, Y., and Ito, N. 1993. Effect of green tea catechins in a rat multi-organ carcinogenesis model. Carcinogenesis 14(8):1549.
Ho, C.-T., Ferraro, T., Chen, Q., and Rosen, R. T. 1994. Phytochemicals in teas and rosemary, and their cancer-preventive properties. In Food Phytochemicals for Cancer Prevention. II. Teas, Spices, and Herbs, (C.T. Ho, T. Osawa and R. T. Rosen, eds.) pp. 2- 19, Am Chemical Soc, Washington, DC.
Ho, Y., Lee, Y. –L., and Hsu, K. –Y. 1995. Dertermination of (+)-catechin in plasma by high-performance liquid chromatography using fluorescent detection. J. Chromatogr. B: Biomed Appl. 665:383-389.
Hodgson, J. M., Morton, L. W., Puddey, I. B., Beilin, L. J., and Croft, K. D. 2000. Gallic acid metabolites are markers of black tea intake in humans. J. Agric. Food Chem. 48:2276-2280.
Hollman, P. C. H., Tijburg, L. B. M., and Yang, C. S. 1997. Bioavailability of flavonoids from tea. Crit. Rev. Food Sci. Nutr. 37(8):719-738.
Hollman, P. C. H., de Vries, J. H. M., van Leeuwen, S. D., Mengelers, M. J. B., and Katan, M. B. 1995. Absorption of dietary quercetin glycosides and quercetin in healthy ileostomy volunteers. Am. J. Clin. Nutr. 62:1276.
Hong. C. Y., Wang, C.p.,Lo, Y.C.,Lo,Y. C., and Hsu, F. L.1994. Effect of flavan-3-01 tannins Purified from Camellia sinensis on lipid peroxidation of rat heart mitochondria. Am Jchinese Med 22:285-292.
Horiba, N., Maekawa, Y., Ito, M. Matsumodo, T., and Nakamura, H. 1991. A pilot study of Japanese green tea as a medicament:antibacterial and bactericidal effects. J. Endodonitics 17(3):122-124.
Huang, M. T., Ho, C. T., Wang, Z. Y., Ferraro, T., Finnegan-Oliver, T., lou, Y. R., Mitchell, J. M., Laskin, J. D., Newmark, H., Yang, C. S., and Conney, A. H. 1992. Inhibitory effect of topical application of a green tea polyphenol fraction on tumor initiation and promotion in mouse skin. Carcinogenesis 13:947.
Huang, M. T., Ferraro, T., and Ho, C. T. 1994. Cancer chemoprevention by phytochemicals in fruits and vegetables. In “Food phytochemicals for Cancer Prevention I”(Ed. Huang, et al.,)ACS Symposium Series 546. pp.2-16.
Huang, M. T., Ferraro, at., and Ho, C. T. 1994. Cancer chemoprevention by phytochemicals in fruits and vegetables. In “Food phytochemicals for Cancer Prevention I”(Ed. Huang, et al.,)ACS Symposium Series 546. pp.2-16.
Ikigai, H., Nakae, T., Hara, Y. and Shimamura, T. 1993. Bactericidal catechins damage the lipid bilayer. Biochimica Biophysica Acta 1147:132-136.
International Agency for Research on Cancer. 1991. IARC monographs on the evaluation of carcinogenic risks to humans. Volume 51. Coffee, Tea, Mate, Methylxanthines and Methylglyoxal. Lyon, France:IARC pp.212-216, 240-263.
Jankun, J., Selman, S. H., and Swiercz, R. 1997. Why drinking green tea could prevent cancer. Nature, 387(5):561.
Katiyar, S. K., Agarwal, R., Wood, G. S., and Mukhtar, H. 1992. Inhibition of 12-o-tetradecanoylphorbol-13-acetate-caused tumor promotion in 7,12-dimethylbenz[a]anthracene-initiated SENCAR mouse skin by a polyphenolic fraction isolated from green tea. Cancer Res. 52:6890-6897.
Katiyar,S.K., and Mukhtar, H. 1997. Inhibition of phorbol ester tumor promoter 12-o-tetradecanoylphorbol-13-acetate-caused inflammatory responses in SENCAR mouse skin by black tea polyphenols. Carcinogenesis. 18:1911-1916.
Kim, M., Hagiwara, N., Smith, S. J., Yamamoto, T., Yamane, T., and Takahashi, T. 1994. Preventive effect of green tea polyphenol on colon carcinogenesis. In “Food phytochemicals for Cancer Prevention II”(Ed. Ho, C. T. et al.,) ACS Symposium Series 547.pp.51-55.
King, R. A., Broadbent, J. L., and Head, R. J. 1996. Absorption and excretion of the soy isoflavone genistein in rats. J. Nutr. 126:176-182.
Kivits, G. A. A., van der Sman, F., and Tijburg, L. B. M. 1997. Analysis of catechins from green and black tea in humans. Int. J. Food Sci. Nutr. In press.
Klaunig, J. E. 1992. Chemopreventive effects of green tea components on hepatic carcinogenesis. Preventive Med 21:510-519.
Li, C., Lee, M. –J., Sheng, S., Meng, X., Prabhu, S., Winnik, B., Huang, B., Chung, J. Y., Yan, S., Ho, C. -T., and Yang, C. S. 2000. Structural identification of two metabolites of catechins and their kinetics in human urine and blood after tea ingestion. Chem. Res. Toxicol. 13:177-184.
Lee, M. –J., Prabhu, S., Meng, X., Li, C., 2000. An improved method for the determination of green and black tea polyphenols in biomatrices by high-performance liquid chromatography with coulometric array detection. Anal. Biochem. 279:164-169.
Lee, M. –L., Wang, Z. –Y., Lee, H., Chen, L., Sun, Y., Gobbo, S., Balentine, D. A., and Yang, C. S. 1995. Analysis of plasma and urinary tea polyphenols in human subjects. Cancer Fpidemiol Biomark. Prev. 4:393-399.
Lin, A.M., Chyi, B.Y., Wu, L. Y., Hwang, L. S., and Ho,L. T. 1998. The antioxidative property of green tea against iron-induced oxidative stress in rat brain. Chinese J of Phys. 41(4):189-94.
Lin, Y. –L., and Lin, J. –K. 1997. (-)-Epigallocatechin-3-
gallate blocks the induction of nitric oxide synthase by down-regulating lipopolysaccharide induced activity of transcription factor nuclear factor-χ B. Molecular Pharmacology 52:465-472.
Lotito, S. B. and Fraga, C. G. 1998. (+)-Catechin prevents human plasma oxidation. Free Radic. Biol. Med. 24(3):435-441.
Luo, M., Wahlqvist, M. L., and O’Brien, R. C. 1997. Inhibition of LDL oxidation by green tea extract. Lancet 349:360-1.
Mack, T. M., Yu, M. C., Hanish, R., and Henderson, B. E. 1986. Pancreas cancer and smoking, beverage consumption, and past medical history. J. Natl. Cancer Inst. 76:49-60.
MacMahon, B., Yen, S., and Trichopoulos, D. 1981. Coffee and cancer of the pancreas. N. Engl. J. Med. 304:630-633.
Mai, J., Chambers, L. J. and McDonals, R. E., 1989. Antioxidant compositions. U.S. patent 4,839,187.
Mangiapane, H., Thomson, J., Salter, A., Brown, S., Bell, D., and White, D. A. 1992. The inhibition of low-density lipoprotein by (+)catechin, a naturally occurring flavonoid. Biochem Phamacol 43:445-450.
Matsuzaki, T., Hara, Y., 1985. Antioxidative activity of tea leaf catechins. Nippon Nogeikagaku Kaishi. 59(2):129-134.
Miura, S., Watanabe, J., Tomita, T., Sano, M., and Tomita, I. 1994. Inhibitory effects of tea polyphenols(flavan-3-olderivatives)on Cu2+-mediated oxidative modification of low-density lipoprotein. Biol Pharm. Bull. 17:1567-72.
Nakachi, K., Suemasu, K., Suga, K., Takeo, T., Imai, K., and Higashi, Y. 1998. Influence of drink green tea on breast cancer malignancy among Japanese patients. Jpn. J. Cancer Res. 89(3):254-261
Nakagawa, K. and Miyazawa, T. 1997. Chemiluminescence-high performance liquid chromatographic determination of tea catechin, (-)epigallocatechin-3-gallate, at picomole levels in rat and human plasma. Anal. Biochem. 248:41-49.
Nakagawa, K., Okuda, S., and Miyazawa, T. 1997. Dose-dependent incorporation of tea catechins, (-)-epigallocatechin-3-galla-te and (-)-epigallocatechin, into human plasma. Biosci. Biotecli. Biochemi. 61(12):1981-1985.
Nakane, H. and Ono, K., 1990. Differential inhibitory effects of some catechin derivatives on the activities of human immunodeficiency virus reverse transcriptase and alular deoxyribonudeic and ribonucleic acid polymerases. Biochemistry 29(11):2841-2845
Namiki, M. 1990. Antioxidants antimutagens in food. Food Sci. and Nut. pp.273-300.
Okabe, S., Suganuma, M., Hayashi, M., Sueoka, E., Komori, A., and Fujiki, H. 1997. Mechanisms of growth inhibition of human lung cancer cell, PC-9, by tea polyphenols. Jpn. J. Cancer Res. 88(7):639-643.
Okushio, K., Matsumoto, N., Suzuki, M., Nanjo, F., and Hara, Y. 1995. Absorption of (-)-epigallocatechin gallate into rat portal vein. BioL pharm BUIL 18:190-191.
Okushio, K., Matsumoto, N., Kohri, T., Suzuki, M., Nanjo, F., and Hara, Y. 1996. Absorption of tea catechins into rat portal vein. BioL Pharm. Bull. 19:326-329.
Okushio, K., Suzuki, M., Matsumoto, N., Nanjo, F., and Hara, Y. 1999. Methylation of tea catechins by rat liver homogenates. Biosci. Biotechnol. Biochem. 63(2):430-432.
Petrakis, P. L., Kallianos, A. G., Wender, S. H., and Shetlar, M. R. 1959. Metabolic studies of quercetin labeled with 14C. Arcli. Bioclietn. Biophys. 85:264-271.
Piskula, M. K. and Terao, J. 1998. Accumulation of (-)-epicatechin metabolites in rat plasma after oral administration and distribution of conjugation enzymes in rat tissues. Jul; 128(7):1172-8
Richards, D. M., Dean, R. T. and Jessup, W. 1988. Membrane protein are critical targets in free radical mediated cytolysis. Biochim Biophys Acta 946:281-88.
Saeki, Y., Ito, Y., Shibata, M., Sato,Y., Takazoe, I., and Okuda, K. 1993. Antimicrobial action of green tea extract, flavono flavor and copper chlorophyll against oral bacteria. Bull. Tokyo dent. Coll. 34(1):33-37.
Salah, N., Miller, N. J., Pagana, G., Tijburg, L., Bolwell, G. P., and Rice-Evans, C. 1995. Polyphenolic flavonoids as scavengers of aqueous phase radicals and as chain- breaking antioxidants. Arch Biochem Biophys 322:339-46.
Sanderson, G. W. 1972. The Chemistry of tea and tea manufacturing. Adv. Phytochem. 5:247.
Sfakianos, J., Coward, L., Kirk, M. and Barnes, S. 1997. Intestinal uptake and biliary excretion of the isoflavone genistein in rats. J. Nutr. 127:1260-1268.
Shali, N. A., Curtis, C. G., Powell, G. M., and Roy, A. B. 1991. Sulfation of the flavonoids quercetin and catechin by rat liver. Xenobiotica 21:881-893.
Shaw, I. C. and Griffiths, L. A. 1980. Identification of the major biliary metabolite of (+)-catechin in the rat. Xenobiotica 10:905-911.
Sheila, A. Wisemen, Douglas A., Balentine, and Balz, Frei. 1997. Antioxidants in tea. Crit Rev in Food Sci and Nutri 37(8):705-18.
Shi, S. T., Wang, Z. –Y., Smith, T. J., Hong, J. –Y., Chen, W. –F., Ho, C. –T., and Yang, C. S. 1994. Effects of green tea and black tea on 4-(methylnitrosoamino)-1-(3-pryridyl)-1-butanone bioactivation, DNA methylation, and lung tumorrigenesis in A/J mice. Cancer Res. 54:4641.
Shimamura, T. and Hara, Y. 1992. Method for inhibiting and treating infection caused by influenza virus. US patent. 5,137,992.
Shimamura, T. and Hara, Y. 1992. Method of preventing mycoplasma infection. US patent. 5,104,901.
Suganuma, M., Okabe, S., Kai, Y., Sueoka, N., Sueoka, E., and Fujiki, H. 1999. Synergistic effects of (-)-epigallocatechin gallate with (-)-epicatechin, sulindac, or tamoxifen on cancerpreventive activity in the human lung cancer cell line PC-9. Cancer Res. 59(1):44-47.
Takino, Y., Imagawa, H., Horikawa, H., and Tanaka, A. 1964. The mechianism of tea leaf catechins. III. Formation of a reddish-orange pigment and its spectral relation to some benzotropolone derivateives. Agric Biol Chem. 28:64-71.
Todd, P. H. 1996. Lipid-soluble green tea catechin antioxidant solutions. U.S. patent 5,527,552.
Tournaire, C., Croux, S., Maurette, M., Beck, L., Hocquaux, M., Braun, A. M., and Oliveros, E. 1993. Antioxidant activity of flavonoids: efficiency of singlet oxygen (1 △ g) quenching. J. photochem photobiol Bi Biol 19:205-215.
Ueno, I., Nakano, N., and Hirono, I. 1983. Metabolic fate of [14C]quercetin in the ACI rat. Jpn. J. Exp. Med. 53:41-50.
Unno, T., Kondo, K., Itakura, H., and Takeo, T. 1996. Analysis of (-)epigallocatechin gallate in human seturn obtained after ingestion of green tea. Biosci. Biotecli. Biochemi. 60:2066-2068.
Van het Hof KH., Wiseman, SA., Yang, CS., and Tijburg, LB. 1999. Plasma and lipoprotein levels of tea catechins following repeated tea consumption. Proc of Soci Exp Biol & Med 220(4):203-9.
Vinson, J. A., Dabbagh, Y. A., Serry, M. M. and Jang, J., 1995. Plant flavonoids, especially tea flavonoids, are powerful antioxidant using an in vitro model for heart disease. J Agric Food Chem 43:2798-99.
Vinson, J. A., Jang, J., Dabbagh, Y. A., Serry, M. M. and Cai, S. 1995. Plant polyphenols exihibit lipoprotein bound antioxidant activity using an in vitro oxidation model for heart disease. J Agric Food Chem 43:2798-99.
Wang, Z. Y., Huang, M. T., Ferraro, T., Wong, C. Q., Lou, Y. R., Reuhl, K., Iatropoulos, M. Yang, C. S. and Conney, A. H. 1992. Inhibitory effect of green tea in the drinking water on tumorrigenesis by ultraviolet light and 12-O-tetradecanoylphorbol-13-acetate in the skin of SKH-1 mice. Cancer Res. 52:1162.
Wang, Z. Y., Wang, L. D. Lee, M. J., Ho, C. –T., Huang, M. -T. Conney, A. H., and Yang, C. S. 1995. Inhibition of N-nitrosomethylbenzylamine-induced esophageal tumorigenesis in rats by green and black tea. Carcinogenesis 16:2143-2148.
Wang, Z. Y., Wang, L. D. Lee, M. J., Ho, C. –T., Huang, M. T. H. C. A., and Yang, C. S. 1995. Inhibition of N-nitrosomethylbenzylamine-induced esophageal tumorigenesis in rats by green and black tea. Carcinogenesis 16:2143.
Wolk, A., Gridley, G., Shelley, N. et al. 1996. International renal cell cancer study: VII. Role of diet. Int. J. Cancer 65:67-73.
Whysner, J., Wang, C. X., Zang, E., Iatropoulos, M. J. and Williams, G. M. 1994. Dose response of promotion by butylated hydroxyanisole in chemically initiated tumours of the rat forestomach. Food and chemical toxicology. 32(3):215-222.
Yamane, T., hagiwara, N., Tateishi, M., Akachi, S., Kim, M., Okuzumi, J., Kitao, Y., Inagake, M., Kuwata, K., and Takahashi, T. 1991. Inhibition of azoxymethane-induced colon carcinogenesis in rat by green tea polyphenol fraction. Jpn. J. Cancer Res. 82(12):1336.
Yang, C. S., Chen, L., Lee, M. –L., Balentine, D., Kuo, M. C., and Schantz, S. P. 1998. Blood and urine levels of tea polyphenols after ingestion of different amounts of tea by human volunteers. 7(4):351-4.
Yang, C. S., Yang, G. –Y., Lee, M. –L., and Chen, L. 1997. Mechanistic considerations of the inhibition of carcinogenesis by tea. In: H. Ogashi, Eds., Proceedings of the International Conference on Food Factors in Cancer Prevention, pp. 113-117. Tokyo: Sptinger-Veriag.
Yang, T. T. and Koo, M. W. 1997. Hypocholesterolemic effect of Chinese tea. Pharma. Res. 35(6):505-12.
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