Increased hexokinase II expression in the renal glomerulus of mice in response to arsenic

被引:14
作者
Pysher, Michele D.
Sollome, James J.
Regan, Suzanne
Cardinal, Trevor R.
Hoying, James B.
Brooks, Heddwen L.
Vaillancourt, Richard R.
机构
[1] Univ Arizona, Coll Pharm, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Biomed Engn, Tucson, AZ 85721 USA
[3] Univ Arizona, Dept Physiol, Tucson, AZ 85721 USA
关键词
arsenic; arsenite; hexokinase;
D O I
10.1016/j.taap.2007.06.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epidemiological studies link arsenic exposure to increased risks of cancers of the skin, kidney, lung, bladder and liver. Additionally, a variety of non-cancerous conditions such as diabetes mellitus, hypertension, and cardiovascular disease have been associated with chronic ingestion of low levels of arsenic. However, the biological and molecular mechanisms by which arsenic exerts its effects remain elusive. Here we report increased renal hexokinase II (HKII) expression in response to arsenic exposure both in vivo and in vitro. In our model, HKII was up-regulated in the renal glomeruli of mice exposed to low levels of arsenic (10 ppb or 50 ppb) via their drinking water for up to 21 days. Additionally, a similar effect was observed in cultured renal mesangial cells exposed to arsenic. This correlation between our in vivo and in vitro data provides further evidence for a direct link between altered renal HKII expression and arsenic exposure. Thus, our data suggest that alterations in renal HKII expression may be involved in arsenic-induced pathological conditions involving the kidney. More importantly, these results were obtained using environmentally relevant arsenic concentrations. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
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