Butyrate reduces the frequency of micronuclei in human colon carcinoma cells in vitro

被引:12
|
作者
Hovhannisyan, Galina [2 ]
Aroutiounian, Rouben [2 ]
Glei, Michael [1 ]
机构
[1] Univ Jena, Biol Pharmaceut Fac, Inst Nutr, Dept Nutr Toxicol, D-07743 Jena, Germany
[2] Yerevan State Univ, Dept Genet & Cytol, Fac Biol, Yerevan 375025, Armenia
关键词
Butyrate; Ferric nitrilotriacetate (Fe-NTA); Hydrogen peroxide (H2O2); Human colon carcinoma cells; Cytokinesis-block micronucleus (CBMN) test; CHAIN FATTY-ACIDS; PERIPHERAL-BLOOD LYMPHOCYTES; GLUTATHIONE S-TRANSFERASES; HT29; CLONE; 19A; DNA-DAMAGE; TUMOR-CELLS; SODIUM-BUTYRATE; HYDROGEN-PEROXIDE; OXIDATIVE STRESS; COMET ASSAY;
D O I
10.1016/j.tiv.2009.06.011
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Butyrate, formed by bacterial fermentation of plant foods, has been shown to protect human colon cells from selected genotoxic substances. The mechanism for this effect could be the enhancement of toxicological defence leading to an increased detoxification of genotoxic risk factors and thus to a reduction of DNA and chromosome damage. Previous protective properties of butyrate against DNA damage induction in colon cells were demonstrated using the comet assay. in the present study the effect of butyrate on chromosome damage induced by ferric nitrilotri acetate (Fe-NTA) and hydrogen peroxide (H2O2) (Suggested to be putative risk factors of colorectal carcinogenesis) was investigated using the cytokinesis-block micronucleus (CBMN) test It was possible to reveal that pre-treatment of HT29 colon carcinoma cells with butyrate (2 and 4 mM) for 15 min caused a reduction of micronuclei induced with H2O2 (75 mu M; p < 0.01) and Fe-NTA (500 and 1000 mu M; p < 0.05). The decrease in the level of Fe-NTA- and H2O2-induced micronuclei was also confirmed in most of the corresponding variants of 24 h pre-treatment of cells with butyrate. The results obtained demonstrate for the first time protective properties of butyrate against chromosome damage induced by H2O2 and Fe-NTA in human colon carcinoma cells. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1028 / 1033
页数:6
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