Clotrimazole, but not dexamethasone, is a potent in vitro inhibitor of cytochrome P450 isoforms CYP1A and CYP3A in rainbow trout
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23466084
DOI
10.1016/j.chemosphere.2013.01.050
PII: S0045-6535(13)00166-5
Knihovny.cz E-resources
- Keywords
- 7-benzyloxy-4-trifluoromethylcoumarin, 7-benzyloxy-4-trifluoromethylcoumarin O-debenzylase, 7-benzyloxyquinoline, BFC, BFCOD, BQ, BzRes, CLO, CYP1A, CYP2E1-like protein, CYP3A, Clotrimazole, DBF, DEX, Dexamethasone, EROD, P450, PNP, PNPH, Rainbow trout, benzyloxyresorufin, clotrimazole, cytochrome P450, dexamethasone, dibenzylfluorescein, ethoxyresorufin O-deethylase, p-nitrophenol, p-nitrophenol hydroxylase,
- MeSH
- Cytochrome P-450 CYP1A1 antagonists & inhibitors metabolism MeSH
- Cytochrome P-450 CYP2E1 metabolism MeSH
- Cytochrome P-450 CYP3A metabolism MeSH
- Dexamethasone chemistry pharmacology MeSH
- Cytochrome P-450 CYP2E1 Inhibitors MeSH
- Cytochrome P-450 CYP3A Inhibitors MeSH
- Cytochrome P-450 Enzyme Inhibitors MeSH
- Microsomes, Liver drug effects enzymology MeSH
- Kinetics MeSH
- Clotrimazole chemistry pharmacology MeSH
- Oncorhynchus mykiss metabolism MeSH
- Cytochrome P-450 Enzyme System metabolism MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cytochrome P-450 CYP1A1 MeSH
- Cytochrome P-450 CYP2E1 MeSH
- Cytochrome P-450 CYP3A MeSH
- Dexamethasone MeSH
- Cytochrome P-450 CYP2E1 Inhibitors MeSH
- Cytochrome P-450 CYP3A Inhibitors MeSH
- Cytochrome P-450 Enzyme Inhibitors MeSH
- Clotrimazole MeSH
- Cytochrome P-450 Enzyme System MeSH
The effects of clotrimazole (CLO) and dexamethasone (DEX), both detected in the aquatic environment, were assessed on inhibition of cytochrome P450 (CYP450) in hepatic microsomes of rainbow trout. Activity of three CYP450 isoforms: ethoxyresorufin O-deethylase (EROD; CYP1A), 7-benzyloxy-4-trifluoromethylcoumarin O-debenzylase (BFCOD; CYP3A) and p-nitrophenol hydroxylase (PNPH; CYP2E1-like protein) was investigated in the presence of four concentrations of CLO and DEX. Clotrimazole in a concentration range of 1-100μM decreased the activity of EROD and BFCOD. The inhibition was reversible, as pre-incubation of the microsomes with CLO, before addition of the substrate, had no effect. EROD activity was non-competitively inhibited with a Ki of 0.5μM, and BFCOD activity revealed competitive inhibition with a Ki of 0.04μM. The relatively low Ki for CLO inhibition of EROD and BFCOD activity may indicate that the ability of CYP1A and CYP3A to metabolize xenobiotics is reduced in the presence of CLO. PNPH activity was not affected by CLO. DEX showed no inhibitory potency on any investigated reaction. CLO, but not DEX, inhibited EROD and BFCOD activity by different mechanisms.
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