Protective effect of (-)-epigallocatechin-3-gallate on capsaicin-induced DNA damage and oxidative stress in human erythrocyes and leucocytes in vitro

被引:11
作者
Pandir, Dilek [1 ]
机构
[1] Bozok Univ, Fac Arts & Sci, Dept Biol, TR-66100 Yozgat, Turkey
关键词
CAP; (-)-Epigallocatechin-3-gallate; Human blood cells; Comet assay; CELL GEL-ELECTROPHORESIS; COMET ASSAY; GREEN TEA; EPIGALLOCATECHIN-3-GALLATE; GENOTOXICITY; TOXICITY; CARCINOGENESIS; MUTAGENICITY; POLYPHENOLS; CATECHINS;
D O I
10.1007/s10616-014-9695-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The aim of this study is to show that protective effects of the main catechin (-)-epigallocatechin-3-gallate (EGCG) against capsaicin (CAP) induced oxidative stress and DNA damage in human blood in vitro. Superoxide dismutase, catalase, glutathione peroxidase and malondialdehyde (MDA) level were studied in erythrocytes and leucocytes with increased concentrations of CAP. DNA damage in leucocytes was measured by the comet assay. Human blood cells have been administered with doses between 0 and 200 mu M of CAP and/or EGCG (20 mu M) for an hour at 37 A degrees C. Treatment with CAP alone has increased the levels of MDA and decreased antioxidant enzymes in human blood cells. A significant increase in tail DNA%, mean tail length and tail moment indicating DNA damage has been observed at the highest dose of CAP treatment when compared to controls. Treatment of cells with CAP plus EGCG prevented CAP-induced changes in antioxidant enzyme activities and MDA level and mean tail lenght indicating DNA damage. A significant increase in mean tail lenght was observed at high doses of CAP. These data suggest that EGCG can prevent toxicity to human erythrocytes and leucocytes caused by CAP, only at low doses.
引用
收藏
页码:367 / 377
页数:11
相关论文
共 63 条
[11]   Effects of 2,4-D and its metabolite 2,4-dichlorophenol on antioxidant enzymes and level of glutathione in human erythrocytes [J].
Bukowska, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2003, 135 (04) :435-441
[12]   The protective role of curcumin on perfluorooctane sulfonate-induced genotoxicity: Single cell gel electrophoresis and micronucleus test [J].
Celik, Ayla ;
Eke, Dilek ;
Ekinci, Seda Yaprak ;
Yildirim, Seda .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 53 :249-255
[13]   Epigallocatechin-3-gallate delivers hydrogen peroxide to induce death of ovarian cancer cells and enhances their cisplatin susceptibility [J].
Chan, MM ;
Soprano, KJ ;
Weinstein, K ;
Fong, D .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 207 (02) :389-396
[14]   CAPSAICIN - IDENTIFICATION, NOMENCLATURE, AND PHARMACOTHERAPY [J].
CORDELL, GA ;
ARAUJO, OE .
ANNALS OF PHARMACOTHERAPY, 1993, 27 (03) :330-336
[15]  
Cotelle S, 1999, ENVIRON MOL MUTAGEN, V34, P246
[16]   A review of the health effects of green tea catechins in in vivo animal models [J].
Crespy, V ;
Williamson, G .
JOURNAL OF NUTRITION, 2004, 134 (12) :3431S-3440S
[17]   (-)Epigallocatechingallate protects the mitochondria against the deleterious effects of lipids, calcium and adenosine triphosphate in isoproterenol induced myocardial infarcted male Wistar rats [J].
Devika, P. T. ;
Prince, P. Stanely Mainzen .
JOURNAL OF APPLIED TOXICOLOGY, 2008, 28 (08) :938-944
[18]   Evaluation of the antigenotoxic potential of monomeric and dimeric flavanols, and black tea polyphenols against heterocyclic amine-induced DNA damage in human lymphocytes using the Comet assay [J].
Dhawan, A ;
Anderson, D ;
de Pascual-Teresa, S ;
Santos-Buelga, C ;
Clifford, MN ;
Ioannides, C .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2002, 515 (1-2) :39-56
[19]  
DRABKIN DL, 1946, J BIOL CHEM, V164, P703
[20]   THE COMET ASSAY - A COMPREHENSIVE REVIEW [J].
FAIRBAIRN, DW ;
OLIVE, PL ;
ONEILL, KL .
MUTATION RESEARCH-REVIEWS IN GENETIC TOXICOLOGY, 1995, 339 (01) :37-59