In vitro effects of the citrus flavonoids diosmin, naringenin and naringin on the hepatic drug-metabolizing CYP3A enzyme in human, pig, mouse and fish
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27107807
DOI
10.1016/j.bcp.2016.04.011
PII: S0006-2952(16)30065-X
Knihovny.cz E-resources
- Keywords
- CYP3A, Diosmin, Diosmin (PubChem CID: 5353588), Inhibition, Naringenin, Naringenin (PubChem CID: 932), Naringin, Naringin (PubChem CID: 25075),
- MeSH
- Citrus chemistry MeSH
- Cytochrome P-450 CYP3A genetics metabolism MeSH
- Diosmin pharmacology MeSH
- Species Specificity MeSH
- Gene Expression MeSH
- Flavanones pharmacology MeSH
- Hydrolysis MeSH
- Enzyme Inhibitors pharmacology MeSH
- Microsomes, Liver drug effects enzymology MeSH
- Liver drug effects enzymology MeSH
- Kinetics MeSH
- Coumarins metabolism MeSH
- Humans MeSH
- Mice, Inbred ICR MeSH
- Mice MeSH
- Oncorhynchus mykiss MeSH
- Swine MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 7-benzyloxy-4-trifluoromethylcoumarin MeSH Browser
- Cytochrome P-450 CYP3A MeSH
- Diosmin MeSH
- Flavanones MeSH
- Enzyme Inhibitors MeSH
- Coumarins MeSH
- naringenin MeSH Browser
- naringin MeSH Browser
Flavonoids are known to have effects on cytochrome P450 enzymatic activity. However, little effort has been made to examine species differences and the relevance of studies on mammalian and fish microsomes so that extrapolations can be made to humans. Therefore, the effects of several naturally occurring flavonoids on the activity of CYP3A-dependent 7-benzyloxy-4-trifluoromethylcoumarin O-debenzylase (BFCOD) were evaluated in human, pig, mouse, and juvenile rainbow trout sources of hepatic microsomes. Each was exposed to three concentrations (1, 10, and 100μM) of diosmin, naringin, and naringenin. Naringenin competitively inhibited BFCOD activity (Ki values were 24.6μM in human, 15.6μM in pig, and 19.6μM in mouse microsomes). In fish, BFCOD activity was inhibited in a noncompetitive manner (Ki=7μM). Neither diosmin nor naringenin affected BFCOD activity in hepatic microsomes from the studied model organisms. These results suggest that dietary flavonoids potentially inhibit the metabolism of clinical drugs.
References provided by Crossref.org