Effects of acetone, acetonitrile, ethanol, methanol and DMSO on cytochrome P450 in rainbow trout (Oncorhynchus mykiss) hepatic microsomes
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26275123
PII: 10.3109/15376516.2015.1074326
Knihovny.cz E-resources
- Keywords
- CYP1A1, CYP2E1, CYP3A, enzyme activity, organic solvent,
- MeSH
- Acetone pharmacology MeSH
- Acetonitriles pharmacology MeSH
- Dimethyl Sulfoxide pharmacology MeSH
- Ethanol pharmacology MeSH
- Isoenzymes MeSH
- Microsomes, Liver drug effects enzymology MeSH
- Liver drug effects enzymology MeSH
- Kinetics MeSH
- Methanol pharmacology MeSH
- Oncorhynchus mykiss metabolism MeSH
- Solvents pharmacology MeSH
- Substrate Specificity MeSH
- Cytochrome P-450 Enzyme System metabolism 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
- Acetone MeSH
- acetonitrile MeSH Browser
- Acetonitriles MeSH
- Dimethyl Sulfoxide MeSH
- Ethanol MeSH
- Isoenzymes MeSH
- Methanol MeSH
- Solvents MeSH
- Cytochrome P-450 Enzyme System MeSH
In vitro impacts of five organic solvents on cytochrome P450 (CYP450) enzyme activity were investigated using hepatic microsomes of rainbow trout. The rates of several CYP450-mediated reactions were investigated at solvent concentrations ranging from 0.01% to 3%. The solvents greatly affected all tested reactions. In at least 0.8% ethanol, 2% methanol or acetone, 1% acetonitrile or 3% dimethyl sulfoxide (DMSO), 7-ethoxyresorufin-O-deethylase (EROD) activity decreased and at 3% acetonitrile or ethanol, it was undetected. At 3%, all tested solvents except methanol reduced 7-benzyloxy-4-trifluoromethylcoumarin-O-debenzylase (BFCOD) activity, but at low concentrations of ethanol (2% and lower) or DMSO (1% and lower), it was induced. This was not seen with the inclusion of a pre-incubation step. p-Nitrophenolhydroxylase (PNPH) activity was not affected at concentrations below 1% DMSO, and at 2% acetonitrile it was reduced, as it was above 1% methanol or 0.5% ethanol. Acetone did not affect PNPH activity with or without a pre-incubation step. In general, the degree of inhibition was similar with and without the pre-incubation step. We conclude that the concentration of organic solvent for solubilizing the substrate and inhibitor in in vitro microsomal studies should be minimized.