Protective effects of selenium on oxidative damage and oxidative stress related gene expression in rat liver under chronic poisoning of arsenic

被引:68
作者
Xu Zhao [1 ,2 ]
Wang Zhou [3 ]
Li Jian-jun [2 ]
Chen Chen [4 ]
Zhang Ping-chuan [1 ]
Dong Lu [1 ]
Chen Jing-hong [1 ]
Chen Qun [1 ]
Zhang Xiao-tian [1 ]
Wang Zhi-lun [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, MinistEduc, Key Lab Environm & Genes Related Dis, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Sci, Dept Chem, Xian 710049, Shaanxi, Peoples R China
[3] Shenzhen Ctr Dis Control & Prevent, Shenzhen 518055, Peoples R China
[4] Univ Queensland, Sch Biomed Sci, Brisbane, Qld 4072, Australia
基金
中国国家自然科学基金; 澳大利亚国家健康与医学研究理事会;
关键词
Na2SeO3; NaAsO2; Liver; Oxidative stress; HSPs; DRINKING-WATER; SODIUM SELENITE; EXPOSURE; HEALTH; PROTEINS; DNA; SUPPLEMENTATION; THIOREDOXIN; ACTIVATION; BIOMARKERS;
D O I
10.1016/j.fct.2013.03.048
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Arsenic (As) is a toxic metalloid existing widely in the environment, and chronic exposure to it through contaminated drinking water has become a global problem of public health. The present study focused on the protective effects of selenium on oxidative damage of chronic arsenic poisoning in rat liver. Rats were divided into four groups at random and given designed treatments for 20 weeks. The oxidative damage of liver tissue was evaluated by lipid peroxidation and antioxidant enzymes. Oxidative stress related genes were detected to reflect the liver stress state at the molecular level. Compared to the control and Na2SeO3 groups, the MDA content in liver tissue was decreased and the activities of antioxidant enzymes were increased in the Na2SeO3 intervention group. The mRNA levels of SOD1, CAT, GPx and Txnrd1 were increased significantly (P < 0.05) in the combined Na2SeO3 + NaAsO2 treatment group. The expressions of HSP70 and HO-1 were significantly (P < 0.05) increased in the NaAsO2 group and reduced in the combined treatment group. The results indicate that long-term intake of NaAsO2 causes oxidative damage in the rat liver, and Na2SeO3 protects liver cells by adjusting the expression of oxidative stress related genes to improve the activities of antioxidant enzymes. Crown Copyright (C) 2013 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 69 条
[1]   Focus on mammalian thioredoxin reductases - Important selenoproteins with versatile functions [J].
Arner, Elias S. J. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2009, 1790 (06) :495-526
[2]   Sodium Arsenite-Induced Alteration in Hepatocyte Function of Rat with Special Emphasis on Superoxide Dismutase Expression Pathway and its Prevention by Mushroom Lectin [J].
Bera, Asit K. ;
Rana, Tanmoy ;
Bhattacharya, Debasis ;
Das, Subhashree ;
Pan, Diganta ;
Das, Subrata K. .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2011, 109 (04) :240-244
[3]   Chromosome damage induced by selenium salts in human peripheral lymphocytes [J].
Biswas, S ;
Talukder, G ;
Sharma, A .
TOXICOLOGY IN VITRO, 2000, 14 (05) :405-408
[4]   Prevention of cytotoxic effects of arsenic by short-term dietary supplementation with selenium in mice in vivo [J].
Biswas, S ;
Talukder, G ;
Sharma, A .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 1999, 441 (01) :155-160
[5]   THIOBARBITURIC ACID REACTION IN RELATION TO FATTY LIVERS [J].
BLOOM, RJ ;
WESTERFELD, WW .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1971, 145 (02) :669-+
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   Effect of dietary co-administration of sodium selenite on sodium arsenite-induced ovarian and uterine disorders in mature albino rats [J].
Chattopadhyay, S ;
Pal, S ;
Ghosh, D ;
Debnath, J .
TOXICOLOGICAL SCIENCES, 2003, 75 (02) :412-422
[8]   Biomarkers of exposure, effect, and susceptibility of arsenic-induced health hazards in Taiwan [J].
Chen, CJ ;
Hsu, LI ;
Wang, CH ;
Shih, WL ;
Hsu, YH ;
Tseng, MP ;
Lin, YC ;
Chou, WL ;
Chen, CY ;
Lee, CY ;
Wang, LH ;
Cheng, YC ;
Chen, CL ;
Chen, SY ;
Wang, YH ;
Hsueh, YM ;
Chiou, HY ;
Wu, MM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 206 (02) :198-206
[9]  
Chen Q., 2009, J TOXICOL SCI, V213, P381
[10]   MEASUREMENT OF CATALASE ACTIVITY IN TISSUE EXTRACTS [J].
COHEN, G ;
DEMBIEC, D ;
MARCUS, J .
ANALYTICAL BIOCHEMISTRY, 1970, 34 (01) :30-+