儿茶素对黑色素形成抑制效果初探
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摘要
儿茶素是2-苯基苯并吡喃的衍生物,属于黄烷醇类化合物。它大量存在于茶树新稍中,占茶叶干重的12%-24%,是多酚类的主要成分,约为总量的70%-80%。根据结构不同,儿茶素分为表儿茶素(EC)、表没食子儿茶素(EGC)、表儿茶素没食子酸酯(ECG)、表没食子儿茶素没食子酸酯(EGCG)。由于结构中具有连或邻苯酚基,儿茶素具有良好的抗氧化能力,其相同物质的量浓度的儿茶素抗氧化能力依次为L-EGCG>L-EGC>L-ECG>L-EC。黑色素的过速增长或分布不均会造成皮肤局部过黑及色素沉着,从而产生雀斑、老年斑、黑斑病等病症,影响美观。酪氨酸酶(EC,1.14.18.1)又称多酚氧化酶,是一种铜蛋白,其活性中心的双核铜离子在酶催化中起重要作用,是黑色素生成的关键酶。随着化妆品及药品行业的发展,天然产物化妆品及药品顺应了回归大自然的发展潮流和人们的消费需求,将成为化妆品及药品开发中的主题。
     本文初步探讨儿茶素对黑色素形成的影响,包括儿茶素对马铃薯酪氨酸酶活性的抑制作用;儿茶素对蘑菇酪氨酸酶活性的抑制作用;EGCG对B16小鼠黑素瘤细胞的形态、细胞增殖率、酪氨酸酶活性及黑色素生成量的影响。取得结果如下:
     一、采用分光光度计法测定酶液加入量、底物浓度、温度、pH值对酶活力的影响,确定最适反应条件。在30℃、pH 6.8的Na2HPO4-NaH2PO4缓冲体系中,采用酶动力学方法研究了儿茶素对马铃薯酪氨酸酶的抑制效应。结果表明:反应最适条件为酶液加入量0.5 mL、底物浓度2 mmol/L、温度30℃、pH 6.8。儿茶素对马铃薯酪氨酸酶有抑制作用,抑制率达到50%的儿茶素质量浓度(IC50)约为0.27 mg/mL; Lineweaver-Burk图显示儿茶素对马铃薯酪氨酸酶的抑制作用表现为竞争型抑制,抑制常数(K1)为0.16 mg/mL。
     二、在30℃,pH 6.8的Na2HPO4-NaH2PO4缓冲体系中,采用酶动力学方法研究了儿茶素对蘑菇酪氨酸酶单酚酶和二酚酶的抑制效应。结果表明,儿茶素对酪氨酸酶单酚酶和二酚酶均有抑制作用,其半数抑制浓度(IC50)约分别为0.89 mg/mL和1.13 mg/mL; Lineweaver-Burk图显示儿茶素对二酚酶的抑制作用表现为竞争型抑制,抑制常数(K1)为0.53 mg/mL。
     三、采用倒置显微镜观察EGCG对B16细胞形态的影响,亚甲基蓝法测定EGCG对B16细胞增殖率的影响,L-多巴氧化法测定EGCG对B16细胞酪氨酸酶活力的影响,氢氧化钠裂解法测定EGCG对B16细胞黑色素生成量的影响。结果表明:EGCG作用24 h,高浓度(>60μM)组细胞胞膜融合现象明显;作用72 h,高浓度组大部分细胞死亡。EGCG对B16细胞增殖率、酪氨酸酶活性、黑色素生成量均有显著抑制,呈明显的剂量效应关系;且EGCG抑制B16细胞增殖,IC50为33.99μM。
     以上研究表明,儿茶素具有抑制体外酪氨酸酶的作用,表现为竞争型抑制;EGCG能够显著抑制B16细胞形态、细胞增殖率、酪氨酸酶活性及黑色素生成量。儿茶素对抑制黑色素形成有一定作用,有望开发成为化妆品及药品。
Catechins are 2-phenyl benzopyran derivatives, the compound of flavanol. The large numbers of catechins are in the new shoot of tea tree, which content is 12% to 24% of the dry weight, about 70%-80% of the total tea polyphenols. According to different structures, catechin include epicatechin (EC), epigallocatechin(EGC), epicatechin gallate (ECG), Epigallocatechin gallate(EGCG). As the structure has phenolic base, catechins have excellent antioxidant activity, the same amount of substance concentration catechins of antioxidant activity were L-EGCG> L-EGC> L-ECG> L-EC. Melanin is too fast growth or uneven distributions that lead to black skin and pigmentation, resulting in freckles, age spots, melasmaand other diseases. Tyrosinase (EC,1.14.18.1) is polyphenol oxidase and a copper protein, which the binuclear copper ions play an important role in enzyme catalysis. It is a key enzyme in melanin synthesis. With the development of cosmetics and medicine industry, natural products as cosmetics and medicine conform to the development trend of returning to nature and people's consumption demand, which will become the subject of cosmetic and medicine development.
     This article preliminarily study effect of catechins on the formation of melanin, including inhibitory effect of catechins on potato tyrosinase; inhibitory effect of catechins on mushroom tyrosinase; effect of EGCG on the B16 melanoma cell morphology, proliferation rate, tyrosinase activity and melanogenesis. We get the following results:
     一、The effect of the quantity of enzyme solution, substrate concentation, temperature and pH on the activity of potato tyrosinase was determined by spectrophotometer method. The inhibitory kinetics of catechins on the activity of potato tyrosinase was studied by enzymological kinetic method in a Na2HPO4-NaH2PO4 buffer solution (pH 6.8) and at 30℃. The results showed that the optimal reaction conditions is quantity of enzyme solution 0.5 mL, substrate concentation 2 mmol/L, temperature 30℃, pH 6.8. Catechins can inhibit the activity of potato tyrosinase, and catechins concentration to 50% inhibitory rate (IC50) is 0.27 mg/mL. It was found that the inhibitory effect of catechins on potato tyrosinase is competitive inhibition mode and inhibition constant (KI) of catechins on potato tyrosinase is 0.16 mg/mL by Lineweaver-Burk plots.
     二、The inhibitory kinetics of catechins on the activity of mushroom tyrosinase monophenolase and diphenolase was studied by enzymological kinetic method in a Na2HPO4-NaH2PO4 buffer solution (pH 6.8) and at 30℃. The results showed that catechins can inhibit both the activity of monophenolase and diphenolase, and catechins concentration to 50% inhibitory rate (IC50) are 0.89 mg/mL and 1.13 mg/mL. It was found that the inhibitory effect of the catechins on diphenolase is in a competitive inhibition mode, and inhibition constant (KI) is 0.53 mg/mL by Lineweaver-Burk plots.
     三、Inverted microscope was used to observe B16 cell morphology; methylene bluemethod, L-DOPA oxidation method, NaOH decomposition method respectively was used to study the effect of EGCG on B16 cell proliferation rate, tyrosinase activity and melanogenesis. The results showed that EGCG act on the B16 at 24 h, the high concentration (>60μM) appeared the phenomenon of cell membrane fusion; after 72 h, most of cell were death at this group. EGCG have significantly inhibited B16 on cell proliferation rate, tyrosinase activity, melanogenesis, which is obvious dose-response relationship. And EGCG have inhibited B16 on cell proliferation, catechins concentration to 50% inhibitory rate (IC50) is 33.99μM.
     These studies have shown that catechins can inhibit tyrosinase in vitro, showed competitive inhibition; EGCG could significantly inhibit the B16 murine melanoma cell morphology, cell proliferation rate, tyrosinase activity and melanogenesis. Catechins have a certain role on the inhibition of melanin synthesis, which is expected to develop as cosmetics and medicines.
引文
[1]Gao XH, Zhang L, Wei HC, et al. Efficacy and Safety of Innovative Cosmeceuticals[J]. Clinics in Dermatology,2008,26 (4):367-374.
    [2]Kim YJ, Uyama H. Tyrosinase Inhibitors from Natural and Synthetic Sources:Structure, Inhibition Mechanism and Perspective for the Future[J]. Cellular and Molecular Life Sciences,2005, 62 (15):1707-1723.
    [3]何学民,秦德安.黑色素与酪氨酸酶[J].中国化妆品,1994(3):32-33.
    [4]Prota G. Progress in the Chemistry of Melanins and Related Metabolites[J]. Med Res Rev,1988, 8 (4):525-556.
    [5]Bhatnagar V, Anjaiah S, Puri N, et al. pH of Melanosomes of B16 Murine Melanoma Is Acidic: Its Physiological Importance in the Regulation of Melanin Biosynthesis[J]. Arch Biochem Biophys, 1993,307 (1):183-192.
    [6]张建友,方艳燕,吴晓琴,等.天然活性美白化妆品研究现状及发展前景[J].精细化工,2008,25(1):72-76.
    [7]Park HY, Kosmadaki M, Yaar M, et al. Gilchrest Cellular Mechanisms Regulating Human Melanogenesis[J]. Cellular and Molecular Life Sciences,2009,66 (9):1493-1506.
    [8]宁岭.皮肤的美白[J].日用化学工业,1998(3):24-27.
    [9]Alvaro SF, Jose NR, Francisco GC, et al. Tyrosinase:a Comprehensive Review of Its Mechanism [J]. Biochimica Biophysica Acta,1995,1247 (1):1-11.
    [10]Parvez S, Kang M, Chung HS, et al. Survey and Mechanism of Skin Depigmenting and Lightening Agents [J]. Phytotherapy Research,2006,20 (11):921-934.
    [11]宋康康.抑制剂对酪氨酸酶的效应及其对黑色素生成调控的研究[D].福建:厦门大学化学化工学院,2007.
    [12]Halaban R, Patton RS, Cheng E, et al. Abnormal Acidification of Melanoma Cells Induces Tyrosinase Retention in the Early Secretory Pathway[J]. J Biol Chem,2002,277 (17):14821-14828.
    [13]Aroca P, Garclaborron JC, Solano F, et al. Regulation of Mammalian Melanogenesis. I:Partial Purification and Characterization of a Dopachrome Converting Factor:Dopachrome Tautomerase[J]. Biochim Biophys Acta,1990,1035 (3):266-275.
    [14]Korner AM, Pawelek J. Dopachrome Conversion:a Possible Control Point in Melanin Biosynthesis[J]. J Invest Dermatol,1980,75 (2):192-195.
    [15]Miranda M, Bonfigli A, Zarivio O, et al. Restriction Patterns of Model DNA Treated with 5,6-dihydroxyindole, a Potent Cytotoxic Intermediate of Melanin Synthesis:Effect of u.v. Irradiation[J]. Mutagenesis,1987,2 (1):45-50.
    [16]Chang TS. an Updated Review of Tyrosinase Inhibitors[J]. International Journal of Molecular Sciences,2009,10 (6):2440-2475.
    [17]Fenoll LG, Penalver MJ, Rodriguez JN, et al. Tyrosinase Kinetics:Discrimination between Two Explain the Mechanism of Monophenol and Diphenol Substrates[J]. The International Journal of Biochemistry and cell Biology,2004,36 (2):235-246.
    [18]Sanjust E, Cecchini G, Sollai F, et al.3-hydroxykynurenine as a Substrate/Activator for Mushroom Tyrosinase[J]. Archives Biochemistry and Biophysics,2003,412 (2):272-278.
    [19]Celia JC, Francisco SS, Takeshi K, et al. a New Enzymatic Function in the Melanogenic Pathway[J]. J Biol Chem,1994,269 (27):17993-18001.
    [20]Yokoyama K, Suzuki H, Yasumoto K, et al. Molecular Cloning of and Functional Analysis of a cDNA Coding for Human DOPAchrome Tautomerase/Tyrosinase-related Protein-2[J]. Biochim Biophys Acta,1994,1217 (3):317-321.
    [21]Seiberg M, Paine C, Sharlow E, et al. Inhibition of Melanosome Transfer Results in Skin Lightening[J]. J Invest Dermatol,2000,115 (2):162-167.
    [22]徐学涛.西藏红缨合耳菊提取物的美白机理研究[D].广东:广东工业大学化学工程与轻工学院,2008.
    [23]李航,赵国华,阚建全,等.天然产物对酪氨酸酶的抑制及抑制机理的研究进展[J].日用化学工业,2003,33(6):383-386.
    [24]Prota G. Melanins, Melanogenesis and Melanocytes:Looking at Their Functional Significance from the Chemist's Viewpoint [J]. Pigment Cell Research,2000,13 (4):283-293.
    [25]Krasagakis K, Garbe C, Eberle J, et al. Tumour Necrosis Factors and Several Interleukins Inhibit the Growth and Modulate the Antigen Expression of Normal Human Melanocytes in Vitro[J]. Arch Dermatol Res,1995,287 (3-4):259-265.
    [26]Swope VB, Nedrano EE, Snalara D. Long-term Proliferation of Human Melanocytes Is Supported by the Physiologic Mitogens Alpha-melanotrop in, Endothelin-1, and Basic Fibroblast Growth Factor[J]. Experimental Cell Research,1995,217 (2):453-459.
    [27]江志洁,朱育新,吴奇英,等.黑色素形成机理的新概念及复合美白剂的应用[J].日用化学工业,1998(4):3-51.
    [28]徐良,步平.美白祛斑化妆品及其未来发展[J].日用化学工业,2001(2):42-45.
    [29]Van DB, Naeyaert JM, Lambert J. The Quest for the Mechanism of MelaninTransfer[J]. Traffic,2006,7(7):769-778.
    [30]Victoria MV, Jacqueline M, Wu XF, et al. Influence of α-melanocyte-stimulating hormone and of Ultraviolet Radiation on the Transfer of Melanosomes to Keratinocytes[J]. FASEB Journal, 2002,16 (1):105-107.
    [31]Pape EL, Wakamatsu K, Ito S, et al. Regulation of Eumelanin/Pheomelanin Synthesis and Visible Pigmentation in Melanocytes by Ligands of the Melanocortin 1 Receptor[J]. Pigment Cell Melanoma Research,2008,21 (4):477-486.
    [32]Zalfa AM, Suzuki I, Tada A, et al. The Melanocortin-1 Receptor and Human Pigmentation[J]. Annals New York Academy of Sciences,1999 (885):117-133.
    [33]Kubo I, Ying BP. Phenolic Constituents of California Buckeye Fruit[J]. Phytochemistry,1992 (31):3793-3794.
    [34]Hori I, Nihei K, Kubo I. Structural Criteria for Depigmenting Mechanism of Arbutin[J]. Phytotherapy Research,2004,18 (6):475-479.
    [35]Yang ZQ, Wang ZH, Tu JB, et al. The Mixture of Aloesin and Arbutin Can Significantly Inhibit the Tyrosinase Activity and Melanogenesis of Cultured Human Melanocytes[J]. Nutrition, 1999 (15):946-949.
    [36]Lim YJ, Lee EH, Kang TH, et al. Inhibitory Effects of Arbutin on Melanin Biosynthesis of Melanocyte Stimulating Hormone-induced Hyperpigmentation in Cultured Brownish Guinea Pig[J]. Skin Tissues Archives of Pharmacal Research,2009,32 (3):367-373.
    [37]Kazuhisa S, Takahisa N, Koji N, et al. Inhibitory Effects of a-Arbutin on Melanin Synthesis in Cultured Human Melanoma Cells and a Three-Dimensional Human Skin Model[J]. Biol Pharm Bull, 2004,27 (4):510-514.
    [38]Maeda K, Fukuda M. Arbutin:Mechanism of Its Depigmenting Action in Human Melanocyte Culture[J]. J Pharmacol Exp Ther,1996,276 (2):765-769.
    [39]Funayama M, Arakawa H, Yamamoto R, et al. Effects of Alpha Andbeta Arbutin on Activity of Tyrosinases from Mushroom and Mousemelanoma[J]. J Biosci Biotechnol Biochem,1995,59 (1): 143.
    [40]Jin YH, Lee SJ, Chung MH, et al. Aloesin and Arbutin Inhibit Tyrosinase Activity in a Synergistic Manner Via a Different Action Mechanism[J]. Arch Pharm Res,1999,22(3):232-236.
    [41]姚斌,沈晓兰,潘亚菊.a-熊果苷的研究进展[J].中国现代应用药学杂志,2005,22(1):32-33.
    [42]Yang CS, Sang S, Lambert JD, et al. Possible Mechanisms of the Cancer-preventive Activities of Green Tea[J]. Mol Nutr Food Res,2006,50 (2):170-175.
    [43]No JK, Soung DY, Kim YJ, et al. Inhibition of Tyrosinase by Green Tea Components[J]. Life Science,1999,65 (21):241-246.
    [44]Meeran SM, Akhtar S, Katiyar SK. Inhibition of UVB-Induced Skin Tumor Development by Drinking Green Tea Polyphenols Is Mediated Through DNA Repair and Subsequent Inhibition of Inflammation[J]. Journal of Investigative Dermatology,2009,129 (5):1258-1270.
    [45]贺孟泉,秦守哲.绿茶面膜的研制[J].中国医学美学·美容杂志,1997,6(4):212-213.
    [46]Zykova T, Zhang Y, Zhu F, et al. The Signal Transduction Networks Required for Phosphorylation of STATl at Ser727 in Mouse Epidermal JB6 Cells in the UVB Response and Inhibitory Mechanisms of Tea Polyphenols[J]. Carcinogenesis,2005,26 (2):331-342.
    [47]Fu BQ, Li H, Wang XR, et al. Isolation and Identification of Flavonoids in Licorice and a Study of Their Inhibitory Effects on Tyrosinase[J]. Journal of Agricultural and Food Chenistry,2005, 53 (19):7408-7414.
    [48]傅博强,李欢,王小如,等.甘草黄酮类化合物对酪氨酸酶单酚酶的抑制[J].天然产物研究与开发,2005,17(4):391-395.
    [49]Nerya O, Vaya J, Musa R, et al. Glabrene and Isoliquiritigenin as Tyrosinase Inhibitors from Licorice Roots[J]. Journal of Agricultural and Food Chemistry,2003,51 (5):1201-1207.
    [50]Kim HJ, Seo SH, Lee BG, et al. Identification of Tyrosinase Inhibitors from Glycyrrhiza Uralensis[J]. Planta Medica,2005,71 (8):785-787.
    [51]Jones K, Hughes J, Hong M, et al. Modulation of Melanogenesis by Aloesin:a Competitive Inhibitor of Tyrosinase[J]. Pigment Cell Researeh,2002,15 (5):335-340.
    [52]鲁严,朱文元,谭城,等.芦荟素对melan- a鼠黑素细胞株黑素生成及其相关基因表达的 影响[J].临床皮肤科杂志,2003,32(9):502-505.
    [53]李诚让,朱文元,王大光,等.芦荟素抑制人表皮黑素细胞酪氨酸酶的最佳浓度选择[J].临床皮肤科杂志,2006,35(8):506-508.
    [54]杨壮群,王正辉,荔鹏,等.芦荟苦素对体外培养的黑素细胞影响的实验研究[J].中国美容医学,2003,12(5):464-466.
    [55]Choi S, Park YI, Lee SK, et al. Aloesin Inhibits Hyperpigmentation Induced by UV Radiation[J]. Clinical and Experimental Dermatology,2002,27 (6):513-515.
    [56]宫霞,李全阳.银杏叶提取物对酪氨酸酶活力的抑制作用[J].食品科学,2001,22(12):25-27.
    [57]Han SK, Choi WH, Ann HS, et al. Effects of EGb 761 and Korean Red Ginseng on Melanogenesis in B16F10 Melanoma Cells and Protection Against UVB Irradiation in Murine Skin[J]. Molecular & Cellular Toxicology,2008,4 (1):85-91.
    [58]庄江兴,邱凌,钟雪,等.银杏酸GA1对酪氨酸酶和黑色素瘤细胞的作用[J].厦门大学学报(自然科学版),2009,48(1):103-106.
    [59]Matsuura R, Ukeda H, Sawamura M. Tyrosinase Inhibitory Activity of Citrus Essential Oils[J]. Journal of Agricultural and Food Chemistry,2006,54 (6):2309-2313.
    [60]Zhang CW, Lu YH, Tao L, et al. Tyrosinase Inhibitory Effects and Inhibition Mechanisms of Nobiletin and Hesperidin from Citrus Peel Crude Extracts[J]. Journal of Enzyme Inhibition and Medicinal Chemistry,2007,22 (1):83-90.
    [61]陈桂霞,邱凌,宋康康,等.桑黄素对蘑菇酪氨酸酶的抑制作用[J].厦门大学学报(自然科学版),2006,45(3):424-427.
    [62]王芳.桑叶中酪氨酸酶抑制成分的研究[D].浙江:浙江工商大学食品科学生物技术工程学院,2008.
    [63]龚静,张飞伟,韩锐,等.红景天水提液对酪氨酸酶抑制效果的初步研究[J].四川大学学报(自然科学版),2006,43(2):468-471.
    [64]Park SH, Kim DS, Park SH, et al. Inhibitory Effect of p-coumaric Acid by Rhodiola Sachalinensis on Melanin Synthesis in B16F10 Cells[J]. Pharmazie,2008,63 (4):290-295.
    [65]Shimizu K, Fukunaga S, Yoshikawa K, et al. Screening of Extracts of Japanese Woods for Melanin Biosynthesis Inhibition[J]. Journal of Wood Science,2007,53 (2):153-160.
    [66]Kim YJ, Kang KS, Yokozawa T. The Anti-melanogenic Effect of Pycnogenol by Its Anti-oxidative Actions[J]. Food and Chemical Toxicology,2008,46 (7):2466-2471.
    [67]Momtaz S, Mapunya BM, Houghton PJ, et al. Tyrosinase Inhibition by Extracts and Constituents of Sideroxylon Inerme L. stem bark, Used in South Africa for Skin Lightening[J]. Journal of Ethnopharmacology,2008,119 (3):507-512.
    [68]Hong ES, Nguyen DTM, Nguyen DH,et al. Inhibition of Melanogenesis by Erigeron Canadensis Via Down-regulating Melanogenic Enzymes in B16F10 Melanoma Cells[J]. Korean Jouranl of Chemical Engineering,2008,25 (6):1463-1466.
    [69]Kai H, Baba M, Okuyama T. Inhibitory Effect of Cucumis Sativus on Melanin Production in Melanoma B16 Cells by Downregulation of Tyrosinase Expression [J]. Plantamedica,2008,74 (15): 1785-1788.
    [70]Lu YH, Lin T, Wang ZT, et al. Mechanism and Inhibitory Effect of Galangin and Its Flavonoid Mixture from Alpinia Officinarum on Mushroom Tyrosinase and B16 Murine Melanoma Cells[J]. Journal of Enzyme Inhibition and Medicinal Chemistry,2007,22 (4):433-438.
    [71]Hwang JH, Lee BM. Inhibitory Effects of Plant Extracts on Tyrosinase, L-DOPA Oxidation, and Melanin Synthesis[J]. Journal of Toxicology and Environmental Health-part A-current Issues, 2007,70 (5-6):393-407.
    [72]程科军,陈竞,梁高林,等.Taxiphyllin:苦竹笋中具有酪氨酸酶抑制活性的氰苷[J].天然产物研究与开发,2005,17(6):733-735.
    [73]Yokozawa T, Kim YJ. Piceatannol Inhibits Melanogenesis by Its Antioxidative Actions[J]. Biol Pharm Bull,2007,30 (11):2007-2011.
    [74]Choi MY, Song HS, Hur HS, et al. Whitening Activity of Luteolin Related to the Inhibition of cAMP Pathway in -MSH-stimulated B16 Melanoma Cells[J]. Archives of Pharmacal Research,2008, 31 (9):1166-1171.
    [75]Maeda K, Naitou T, Umishio K, et al. a Novel Melanin Inhibitor:Hydroperoxy Traxastane-type Triterpene from Flowers of Arnica montana[J]. Biol Pharm Bull,2007,30 (5): 873-879.
    [76]Kim HJ, Cho YD, Leem KH, et al. Effects of Ephedrae Herba on Melanogenesis and Gene Expression Profiles Using cDNA Microarray in B16 Melanocytes[J]. Phytotherapy Research,2006, 20 (9):748-754.
    [77]Kim KS, Kim JA, Eom SY, et al. Inhibitory Effect of Piperlonguminine on Melanin Production in Melanoma B16 Cell Line by Downregulation of Tyrosinase Expression [J]. Pigment Cell Research,2006,19 (1):90-98.
    [78]陈龙,陈栋梁,杨国燕,等.鱼胶原肽抑制酪氨酸酶活性能力的比较研究[J].中国美容医学,2008,17(10):1512-1514.
    [79]Tsukamoto T, Ichimaru Y, Kanegae N, et al. Identification and Isolation of Endogenous Insect Phenoloxidase Inhibitors[J]. Biochem Biophys Res Commun,1992,184 (1):86-92.
    [80]Leng B, Liu XD, Chen QX. Inhibitory Effects of Anticancer Peptide from Mercenaria on the BGC-823 Cells and Several Enzymes[J]. FEBS Letters,2005,579 (5):1187-1190.
    [81]Sugumaran M, Nellaiappan K. Characterization of a New Phenoloxidase Inhibitor from the Cuticle of Manduca Sexta[J]. Biochemical and Biophysical Research Communications, 2000,268 (2):379-383.
    [82]Goetghebeur M, Kermasha S. Inhibition of Polyphenol Oxidase by Copper-mentallothionein from Aspergillus Niger[J]. Phytochemistry,1996,42 (4):935-940.
    [83]张大海,李先国,孙炳华.葡萄孢菌代谢产物a-吡喃酮酪氨酸酶抑制活性的研究[J].中国海洋药物杂志,2008,27(3):35-38.
    [84]范羽仪,胡征宇,梅洪.不同念珠藻的提取物对酪氨酸酶活性的抑制作用[J].武汉植物学研究,2008,26(2):179-182.
    [85]Morimura K, Hiramatsu K, Yamazaki C, et al. DaedalinA, a Metabolite of Daedalea dickinsii,Inhibits Melanin Synthesis in an in Vitro Human Skin Model[J]. biosci biotechnol biochem, 2009,73 (3):627-632.
    [86]Park SH, Kim DS, Kim WG, et al. Terrein:a New Melanogenesis Inhibitor and Its Mechanism[J]. Cellular and Molecular Life Sciences,2004,61 (22):2878-2885.
    [87]宛晓春.茶叶生物化学[M].北京:中国农业出版社,2003:9-20.
    [88]李敏,刘磊,郭玉蓉,等.马铃薯多酚氧化酶的特性研究[J].甘肃农业大学学报,2005,40(2):21-24.
    [89]段玉清,刘睿,谢笔钧.莲房原花青素对酪氨酸酶活力和黑色素生物合成影响的初步研究[J].食品科学,2004,25(3):169-174.
    [90]龚盛昭,杨卓如,程江.肉桂酸抑制酪氨酸酶催化反应的动力学研究[J].高校化学工程学报,2007,21(2):345-349.
    [91]邓湘庆,龚盛昭,揭向阳.川芎提取物抑制酪氨酸酶活性的研究[J].中药材,2007,30(4):469-471.
    [92]龚盛昭,杨卓如,程江.香草醛对酪氨酸酶活性的抑制[J].华南理工大学学报:自然科学版,2006,34(5):53-57.
    [93]彭思远,刘轩,柯红梅,等.木贼活性成分对蘑菇酪氨酸酶的抑制作用[J].厦门大学学报:自然科学版,2008,47(S2):115-117.
    [94]Kim DS, Park SH, Kwon SB, et al. (-)-Epigallocatechin-3-gallate and hinokitiol reduce melanin synthesis via decreased MITF production[J]. Arch Pharm Res,2004,27(3):334-339.
    [95]岳学状,朱文元,马慧军.表没食子儿茶素没食子酸酯对人表皮黑素细胞黑素合成的影响及机制[J].临床皮肤科杂志,2005,34(12):795-797.
    [96]Kazuomi S, Masaru T. Depigmenting Effect of Catechins[J]. Molecules,2009,14(11): 4425-4432.
    [97]康琰琰,张美英,邢少璟,等.几种天然活性物对黑色素细胞毒性及美白功效的比较[J].日用化学工业,2005,35(6):361-363.
    [98]蒋亚林.细胞生物学实验[M].上海:复旦大学出版社,1996.
    [99]程宝鸾.动物细胞培养技术[M].广州:华南理工大学出版社,2006.
    [100]Yang J, Liu RH. Synergistic effect of apple extracts and quercetin 3-beta-d-glucoside combination on antiproliferative activity in MCF-7 human breast cancer cells in vitro [J]. Journal of Agricultural and Food Chemistry,2009,57(18):8581-8586.
    [101]Mitsuhashi S, Saito A, Nakajima N, et al. Pyrogallol structure in polyphenols is involved in apoptosis-induction on HEK293T and K562 cells[J]. Molecules,2008,13(12):2998-3006.

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