Impact of long term Fe3+ toxicity on expression of glutathione system in rat liver

被引:25
作者
Budak, Harun [1 ]
Gonul, Nurdan [1 ]
Ceylan, Hamid [1 ]
Kocpinar, Enver Fehim [2 ]
机构
[1] Ataturk Univ, Dept Mol Biol & Genet, Fac Sci, TR-25240 Erzurum, Turkey
[2] Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey
关键词
Iron; Toxic effects; Glutathione system; mRNA expression; Enzyme activity; INDUCED OXIDATIVE STRESS; IRON-DEFICIENCY ANEMIA; CANCER-RISK; MAMMARY-GLAND; S-TRANSFERASE; DIETARY IRON; OVERLOAD; LEAD; METABOLISM; MECHANISMS;
D O I
10.1016/j.etap.2013.12.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The free radicals within the body, produced by metabolic activities or derived from environmental sources are relatively related to hepatoxicity. Since heavy metals including iron have the ability to produce free radicals, the liver glutathione system neutralizes them to protect cells against any damage. The objective of this study is to indicate the toxic effects of iron on the glutathione system at the enzymatic and molecular level. Thus, any possible correlation between enzymatic and molecular levels can be determined. According to our results, while mRNA expression of glutathione reductase (Gsr) and glutathione S-transferases (Gsta5) genes were not affected by long-term exposure to various concentrations of iron (Fe3+), transcription level of glutathione peroxidase (Gpx2) was influenced in the presence of toxic iron. Whereas the enzyme activites of GSR (GR), GPX and GST were significantly affected in rat liver. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:365 / 370
页数:6
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