Comparative oxygen radical formation and toxicity of BDE 47 in rainbow trout cell lines

被引:40
作者
Shao, J. [1 ]
Eckert, M. L. [1 ]
Lee, L. E. J. [2 ]
Gallagher, E. P. [1 ]
机构
[1] Univ Washington, Dept Environm & Occupat Hlth Sci, Seattle, WA 98105 USA
[2] Wilfrid Laurier Univ, Dept Biol, Waterloo, ON N2L 3C5, Canada
关键词
2,2',4,4'-tetrabromodiphenyl ether; rainbow trout; cell lines; reactive oxygen species;
D O I
10.1016/j.marenvres.2008.02.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The polybrominated cliphenyl ethers (PBDEs) constitute a class of flame retardants whose residues have markedly increased in fish and human tissues during the last decade. In particular, the levels of certain PBDE congeners in salmon have raised concern regarding potential risks associated with dietary PBDE exposures. However, little is known regarding PBDE-mediated cell injury in relevant in vitro cell models. We conducted a comparative study of oxyradical production and cell injury in rainbow trout gill (RTgillW1) and trout liver cells (RTL-Wl) exposed to 2,2',4,4'-tetrabromodiphenyl ether (BDE 47), a predominant BDE residue found in fish tissues such as salmonids. Exposure to low micromolar concentrations of BDE 47 elicited a significant loss in RTgill-Wl and RTL-W1 cell viability as measured by alamarBlue assay. The dose-response of BDE toxicity differed among the two cell lines, with the RTL-W1 liver cells showing greater resistance to toxicity at lower BDE 47 doses, but a more dramatic loss of viability relative to gill cells when challenged with higher (50 pM) doses. The sensitivity of the trout liver cells at higher BDE 47 exposures was i -eflected by a higher basal production of oxygen radical production by 6-carboxy2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA) fluorescence that was markedly enhanced in the presence of BDE 47, suggesting an overwhelming of trout liver cell antioxiclant defense pathways. Collectively, our data indicate that RTgill-W1 and RTL-WI liver cells are sensitive to BDE 47-mediated cell injury through a mechanism that may involve oxidative Stress. Our data also provide an in vitro basis for potential tissue differences in BDE 47-mediated cell injury. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 8
页数:2
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