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
[41]   ASSAY FOR LIPID PEROXIDES IN ANIMAL-TISSUES BY THIOBARBITURIC ACID REACTION [J].
OHKAWA, H ;
OHISHI, N ;
YAGI, K .
ANALYTICAL BIOCHEMISTRY, 1979, 95 (02) :351-358
[42]   Evaluation of the cytogenetic damage induced by the organophosphorous insecticide acephate [J].
Ozkan, Deniz ;
Yuzbasioglu, Deniz ;
Unal, Fatma ;
Yilmaz, Serkan ;
Aksoy, Hueseyin .
CYTOTECHNOLOGY, 2009, 59 (02) :73-80
[43]  
Padma Viswanadha Vijaya, 2012, Asian Pacific Journal of Tropical Biomedicine, V2, P910, DOI 10.1016/S2221-1691(12)60252-4
[44]  
PAGLIA DE, 1967, J LAB CLIN MED, V70, P158
[45]  
POOLZOBEL BL, 1992, CLIN INVESTIGATOR, V70, P299
[46]   Antioxidant properties of phenolic compounds [J].
RiceEvans, CA ;
Miller, J ;
Paganga, G .
TRENDS IN PLANT SCIENCE, 1997, 2 (04) :152-159
[47]   Cytotoxicity and genotoxicity of capsaicin in human neuroblastoma cells SHSY-5Y [J].
Richeux, F ;
Cascante, M ;
Ennamany, R ;
Saboureau, D ;
Creppy, EE .
ARCHIVES OF TOXICOLOGY, 1999, 73 (07) :403-409
[48]   CANCER-EPIDEMIOLOGY - THE INDIAN SCENE [J].
SANGHVI, LD .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1981, 99 (1-2) :1-14
[49]   Mechanisms and clinical uses of capsaicin [J].
Sharma, Surinder Kumar ;
Vij, Amarjit Singh ;
Sharma, Mohit .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2013, 720 (1-3) :55-62
[50]   Protective effects of capsaicin against cisplatin-induced nephrotoxicity in rats [J].
Shimeda, Y ;
Hirotani, Y ;
Akimoto, Y ;
Shindou, K ;
Ijiri, Y ;
Nishihori, T ;
Tanaka, K .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (09) :1635-1638