Effects of chronic exposure to tributyltin on tissue-specific cytochrome P450 1 regulation in juvenile common carp
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- Keywords
- CYP450 1 family genes, EROD, fish, tissue-specific response, tributyltin,
- MeSH
- Cytochrome P-450 CYP1A1 metabolism MeSH
- Carps genetics MeSH
- Linear Models MeSH
- RNA, Messenger genetics metabolism MeSH
- Organ Specificity drug effects MeSH
- Gene Expression Regulation, Enzymologic drug effects MeSH
- Cytochrome P-450 Enzyme System genetics metabolism MeSH
- Trialkyltin Compounds toxicity MeSH
- Environmental Exposure * MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cytochrome P-450 CYP1A1 MeSH
- RNA, Messenger MeSH
- Cytochrome P-450 Enzyme System MeSH
- Trialkyltin Compounds MeSH
- tributyltin MeSH Browser
1. The purpose of this study was to compare tributyltin (TBT)-induced cytochrome P450 1 (CYP450 1) regulation in liver, gills and muscle of juvenile common carp (Cyprinus carpio). 2. Fish were exposed to sublethal concentrations of TBT (75, 0.75 and 7.5 μg/L) for 60 days. CYP450 1A was measured at the enzyme activity level as 7-ethoxyresorufin-O-deethylase (EROD) activity, as well as the mRNA expression of CYP450 1 family genes (CYP1A, CYP1B, CYP1C1 and CYP1C2) in fish tissues. 3. Based on the results, the liver displayed the highest absolute levels of EROD activity, both under nonexposed and exposed conditions. Additional, EROD activities and CYP1A gene levels showed a good correlation in all three organs. According to the mRNA expression of CYP450 1 family genes, it suggested that CYP1A was to accommodate most EROD activity in fish, but other CYP450 forms also involved in this proceeding. 4. Overall, the study revealed both similarities and differences in the concentration-dependent CYP450 1 responses of the three target organs, which could provide useful information to better understand the mechanisms of TBT-induced bio-toxicity.
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