Verapamil does not modify catalytic activity of CYP450 in rainbow trout after long-term exposure
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22244749
DOI
10.1016/j.ecoenv.2011.12.012
PII: S0147-6513(11)00469-6
Knihovny.cz E-resources
- MeSH
- Biomarkers metabolism MeSH
- Calcium Channel Blockers toxicity MeSH
- Water Pollutants, Chemical toxicity MeSH
- Microsomes, Liver drug effects enzymology metabolism MeSH
- Liver drug effects enzymology metabolism MeSH
- Coumarins metabolism MeSH
- Nitrophenols metabolism MeSH
- Oncorhynchus mykiss MeSH
- Oxazines metabolism MeSH
- Cytochrome P-450 Enzyme System metabolism MeSH
- Verapamil toxicity MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 4-nitrophenol MeSH Browser
- 7-benzyloxy-4-trifluoromethylcoumarin MeSH Browser
- Biomarkers MeSH
- Calcium Channel Blockers MeSH
- Water Pollutants, Chemical MeSH
- Coumarins MeSH
- Nitrophenols MeSH
- Oxazines MeSH
- pentoxyresorufin MeSH Browser
- Cytochrome P-450 Enzyme System MeSH
- Verapamil MeSH
Little is known about the effects of the cardiovascular drug verapamil (VRP) on metabolic processes in fish. Most calcium channel blockers including VRP are metabolized by cytochrome P450 (CYP450) enzymes. In this study we investigated the in vivo effect of VRP on some CYP450-mediated reactions in juvenile rainbow trout (Oncorhynchus mykiss). Fish were exposed to sublethal concentrations of VRP (0.5, 27 and 270 μg l(-1)) for 0, 21, and 42 day. The following CYP450-mediated reactions were studied in hepatic microsomes: O-dealkylation of ethoxyresorufin, methoxyresorufin, and pentoxyresorufin, hydroxylation of coumarin, tolbutamide, and p-nitrophenol, and O-debenzylation of 7-benzyloxy-4-trifluoromethylcoumarin. The amounts of products of these reactions did not differ among fish exposed to different levels of VRP and control fish. This suggests that the levels of VPR used did not alter catalytic activity of the selected CYP450 enzymes. In conclusion, none of the investigated CYP450-mediated reactions has potential as a biomarker to monitor VRP contamination of the aquatic environment.
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