Arsenic accumulation, elimination, and interaction with copper, zinc and manganese in liver and kidney of rats

被引:48
作者
Cui, Xing [1 ,2 ]
Okayasu, Ryuichi [1 ]
机构
[1] Natl Inst Radiol Sci, Heavy Ion Radiobiol Res Grp, Res Ctr Charged Particle Therapy, Inage Ku, Chiba 2638555, Japan
[2] Natl Inst Environm Studies, Environm Hlth Sci Div, Tsukuba, Ibaraki 3058506, Japan
关键词
Arsenic; Metabolism; Trace element; Metallothionein-1;
D O I
10.1016/j.fct.2008.09.040
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The arsenic accumulation, distribution and influences on metallothionein-1 (MT-1) expression and other trace elements in various organs were examined in rats orally exposed to sodium arsenate (iAs(v)). Rats received a dose of 0, 1, 10 and 100 ppm of iAs(v) in drinking water daily for4- and 16-weeks. Arsenic seems to be distributed in all of the tissues, and was accumulated relatively higher in the spleen, lung and kidney compared to the liver, and much lower in skin and cerebrum. High dose of iAs(v)-exposure significantly increased the concentration of copper in the kidney, but did not influence other trace elements such as zinc and manganese in the liver. The mRNA expression of MT-1 was dose-dependently increased by iAsv-exposure in the liver whereas it was decreased in the kidney. These data indicate that arsenic is widely distributed and significantly accumulated in various organs and influences on other trace elements, and also modulates MT-1 expression in the liver and kidney. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3646 / 3650
页数:5
相关论文
共 24 条
[1]   Arsenic copper interaction in the kidney of the rat: Influence of arsenic metabolites [J].
Ademuyiwa, O ;
Elsenhans, B ;
Nguyen, PT ;
Forth, W .
PHARMACOLOGY & TOXICOLOGY, 1996, 78 (03) :154-160
[2]   Time course of arsenite-induced copper accumulation in rat kidney [J].
Ademuyiwa, O ;
Elsenhans, B .
BIOLOGICAL TRACE ELEMENT RESEARCH, 2000, 74 (01) :81-92
[3]   ARSENIC INDUCES AND ENHANCES RAT HEPATIC METALLOTHIONEIN PRODUCTION INVIVO [J].
ALBORES, A ;
KOROPATNICK, J ;
CHERIAN, MG ;
ZELAZOWSKI, AJ .
CHEMICO-BIOLOGICAL INTERACTIONS, 1992, 85 (2-3) :127-140
[4]  
Campagne MV, 1999, P NATL ACAD SCI USA, V96, P12870
[5]   CANCER POTENTIAL IN LIVER, LUNG, BLADDER AND KIDNEY DUE TO INGESTED INORGANIC ARSENIC IN DRINKING-WATER [J].
CHEN, CJ ;
CHEN, CW ;
WU, MM ;
KUO, TL .
BRITISH JOURNAL OF CANCER, 1992, 66 (05) :888-892
[6]   Family correlations of arsenic methylation patterns in children and parents exposed to high concentrations of arsenic in drinking water [J].
Chung, JS ;
Kalman, DA ;
Moore, LE ;
Kosnett, MJ ;
Arroyo, AP ;
Beeris, M ;
Mazumder, DNG ;
Hernandez, AL ;
Smith, AH .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2002, 110 (07) :729-733
[7]   Arsenic speciation in bile and urine following oral and intravenous exposure to inorganic and organic arsenics in rats [J].
Cui, X ;
Kobayashi, Y ;
Hayakawa, T ;
Hirano, S .
TOXICOLOGICAL SCIENCES, 2004, 82 (02) :478-487
[8]   Subchronic exposure to arsenic through drinking water alters expression of cancer-related genes in rat liver [J].
Cui, X ;
Li, S ;
Shraim, A ;
Kobayashi, Y ;
Hayakawa, T ;
Kanno, S ;
Yamamoto, M ;
Hirano, S .
TOXICOLOGIC PATHOLOGY, 2004, 32 (01) :64-72
[9]   Chronic oral exposure to inorganic arsenate interferes with methylation status of p16INK4a and RASSF1A and induces lung cancer in A/J mice [J].
Cui, Xing ;
Wakai, Toshifumi ;
Shirai, Yoshio ;
Hatakeyama, Katsuyoshi ;
Hirano, Seishiro .
TOXICOLOGICAL SCIENCES, 2006, 91 (02) :372-381
[10]   Stress proteins induced by arsenic [J].
Del Razo, LM ;
Quintanilla-Vega, B ;
Brambila-Colombres, E ;
Calderón-Aranda, ES ;
Manno, M ;
Albores, A .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 177 (02) :132-148