CYP1A expression in liver and gills of rainbow trout (Oncorhynchus mykiss) after short-term exposure to dibenzothiophene (DBT)

被引:16
|
作者
Wozny, Maciej [1 ]
Brzuzan, Pawel [1 ]
Luczynski, Michal K. [2 ]
Gora, Maciej [3 ]
Wolinska, Lidia [1 ]
Bukowski, Rafal [4 ]
Podlasz, Piotr [4 ]
机构
[1] Univ Warmia & Mazury, Fac Environm Sci & Fisheries, Dept Environm Biotechnol, PL-10719 Olsztyn, Poland
[2] Univ Warmia & Mazury, Fac Environm Management & Agr, Dept Chem, PL-10719 Olsztyn, Poland
[3] Jagiellonian Univ, Fac Chem, Dept Organ Chem, PL-30060 Krakow, Poland
[4] Univ Warmia & Mazury, Fac Vet Med, Dept Anim Anat, PL-10719 Olsztyn, Poland
关键词
CYP1A; DBT; Dibenzothiophene; mRNA; Protein; Rainbow trout; MESSENGER-RNA; PROTEIN;
D O I
10.1016/j.chemosphere.2010.01.063
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Dibenzothiophene (DBT), a common component of crude oil, is a widespread environmental pollutant of known adverse effects to aquatic vertebrates. However, the molecular mechanism by which DBT exerts its effects still remains unknown. Our goal for this study was to examine DBT effects on CYP1A expression in liver and gills of rainbow trout after short-term exposure. juvenile trout individuals were injected intraperitoneally with two doses of DBT (10 or 50 mg kg(-1)) and were kept in tanks for 8 and 24 h (T = 14 degrees C), then their gene expression levels were evaluated by Real-Time qPCR and Western-blot analysis. Treatment with DBT at either dose decreased CYP1A mRNA levels through the exposure period, which resulted in the final decrease of CYP1A protein levels in liver and gills on the end of experiment (24 h). Thus, our results showing significant depletion of CYP1A molecules in metabolic tissues upon DBT treatment correlate with those previous reports that indicate a role of DBT in reducing CYP1A activity in fish. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:110 / 112
页数:3
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