Concentrated green tea supplement: Biological activity and molecular mechanisms

被引:33
作者
Cyboran, S. [1 ]
Strugala, P. [1 ]
Wloch, A. [1 ]
Oszmianski, J. [2 ]
Kleszczynska, H. [1 ]
机构
[1] Wroclaw Univ Environm & Life Sci, Dept Phys & Biophys, PL-50375 Wroclaw, Poland
[2] Wroclaw Univ Environm & Life Sci, Dept Fruit Vegetable & Cereal Technol, PL-50375 Wroclaw, Poland
关键词
Green tea supplement; Antioxidant activity; Anti-inflammatory activity; UPLC; Polyphenols; Membrane fluidity; Erythrocytes; Hemolytic activity; EPIGALLOCATECHIN GALLATE; ANTIOXIDANT ACTIVITY; GROWTH-INHIBITION; POLYPHENON-E; CATECHINS; LIPOXYGENASE; ERYTHROCYTES; MEMBRANE; CELLS; INACTIVATION;
D O I
10.1016/j.lfs.2014.12.025
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Aim: This study was undertaken to determine the biological activity of a green tea supplement with respect to cells and erythrocyte membranes and the molecular mechanism of that activity. Main methods: The extract's activity was evaluated on the basis of its hemolytic, antioxidant and anti-inflammatory actions. In addition, the extract's effect on the physical properties of the erythrocyte membrane was examined. We also conducted a detailed analysis of supplement ingredients using high-yield liquid chromatography, supplemented with standard tests of total content of polyphenols and flavonoids in the supplement. Key findings: The study showed that green tea extract has a high antioxidant and anti-inflammatory capacity with no deleterious effect on red blood cells. The extract modifies the physical properties of the erythrocyte membrane, apparently by binding to its hydrophilic region, with consequent rigidity of the hydrophobic region, increased hydration and a moderate increase in its resistance to changes in tonicity of the medium. Because the extract's components anchor in the polar region of membrane lipids, they are able to effectively scavenge free radicals in the immediate vicinity of the membrane and hinder their diffusion into its interior. Significance: Green tea supplement at concentrations markedly exceeding the blood plasma physiological poly-phenol concentrations has no destructive effect on the erythrocyte membrane. Due to the high content of flavan-3-ols, the supplement exhibits high biological activity, which makes it an alternative source of those substances to the commonly used infusion of green tea leaves. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 80 条
[1]
Effect of flavonoid structure on the fluidity of model lipid membranes [J].
Abram, Veronika ;
Berlec, Barbara ;
Ota, Ajda ;
Sentjurc, Marjeta ;
Blatnik, Petra ;
Ulrih, Natasa Poklar .
FOOD CHEMISTRY, 2013, 139 (1-4) :804-813
[2]
Development and validation of fluorescence spectroscopic assays to evaluate antioxidant efficacy. Application to metal chelators [J].
Arora, A ;
Strasburg, GM .
JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1997, 74 (09) :1031-1040
[3]
The chemistry of tea flavonoids [J].
Balentine, DA ;
Wiseman, SA ;
Bouwens, LCM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :693-704
[5]
Application and Analysis of the Folin Ciocalteu Method for the Determination of the Total Phenolic Content from Limonium Brasiliense L. [J].
Blainski, Andressa ;
Lopes, Gisely Cristiny ;
de Mello, Joao Carlos Palazzo .
MOLECULES, 2013, 18 (06) :6852-6864
[6]
Interaction of selected anthocyanins with erythrocytes and liposome membranes [J].
Bonarska-Kujawa, Dorota ;
Pruchnik, Hanna ;
Kleszczynska, Halina .
CELLULAR & MOLECULAR BIOLOGY LETTERS, 2012, 17 (02) :289-308
[7]
Hepatotoxicity associated with supplements containing Chinese green tea (Camellia sinensis) [J].
Bonkovsky, HL .
ANNALS OF INTERNAL MEDICINE, 2006, 144 (01) :68-71
[8]
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[9]
The relationship between the structure and biological actions of green tea catechins [J].
Braicu, Cornelia ;
Ladomery, Michael R. ;
Chedea, Veronica S. ;
Irimie, Alexandru ;
Berindan-Neagoe, Loana .
FOOD CHEMISTRY, 2013, 141 (03) :3282-3289
[10]
Cavet ME, 2011, MOL VIS, V17, P533