Protective activity of the Uncaria tomentosa extracts on human erythrocytes in oxidative stress induced by 2,4-dichlorophenol (2,4-DCP) and catechol

被引:49
作者
Bors, Milena [1 ]
Bukowska, Bozena [1 ]
Pilarski, Radoslaw [2 ]
Gulewicz, Krzysztof [2 ]
Oszmianski, Jan [3 ]
Michalowicz, Jaromir [1 ]
Koter-Michalak, Maria [1 ]
机构
[1] Univ Lodz, Dept Biophys Environm Pollut, PL-90237 Lodz, Poland
[2] Polish Acad Sci, Inst Bioorgan Chem, PL-61704 Poznan, Poland
[3] Wroclaw Univ Environm & Life Sci, Dept Fruit & Vegetable Proc, PL-50375 Wroclaw, Poland
关键词
Uncaria tomentosa; Human erythrocyte; Hemoglobin; Lipid peroxidation; Antioxidant activity; AFFECTED IN-VITRO; RED-BLOOD-CELLS; NF-KAPPA-B; ANTIINFLAMMATORY ACTIVITY; PHENOXYACETIC HERBICIDES; ANTIOXIDANT PROPERTIES; HYDROGEN-PEROXIDE; PLANT METABOLITES; AQUEOUS EXTRACTS; FREE-RADICALS;
D O I
10.1016/j.fct.2011.06.013
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
The purpose of this study was to evaluate the effect of the ethanolic and aqueous extracts of Uncaria tomentosa on human erythrocytes and additionally the assessment of protective effect of these extracts on hemolysis induction, hemoglobin oxidation, and changes in the level of reactive oxygen species (ROS) and lipid peroxidation, which were provoked by selected xenobiotics, i.e. 2,4-dichlorophenol (2,4-DCP) and catechol. All tested extracts, even at a very high concentration of 500 mu g/m1 were not toxic to the erythrocytes because they did not cause lipid peroxidation, increase methemoglobin and ROS levels nor provoked hemolysis. The results of this study also revealed protective effect of extracts of U. tomentosa. The extracts studied depleted the extent of hemoglobin oxidation and lipid peroxidation as well as decreased the level of ROS and hemolysis, which was provoked by 2,4-DCP. No protective activity of the extracts against catechol action, which is a precursor of semiquinones in cell was found. A difference in the effect of the extracts studied was observed. Ethanol-based extracts revealed more pronounced ability to inhibit oxidation processes in human erythrocytes. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2202 / 2211
页数:10
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