Porcine CYP2A19, CYP2E1 and CYP1A2 forms are responsible for skatole biotransformation in the reconstituted system
Language English Country Sweden Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20027142
PII: NEL300709A05
Knihovny.cz E-resources
- MeSH
- Cytochrome P-450 CYP1A2 metabolism MeSH
- Cytochrome P-450 CYP2E1 metabolism MeSH
- Indoles metabolism MeSH
- Cytochrome P-450 CYP1A2 Inhibitors MeSH
- Cytochrome P-450 CYP2E1 Inhibitors MeSH
- Cytochrome P-450 Enzyme Inhibitors MeSH
- Humans MeSH
- Oxindoles MeSH
- Swine MeSH
- Skatole metabolism MeSH
- Cytochrome P-450 Enzyme System metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 3-methyloxindole MeSH Browser
- Cytochrome P-450 CYP1A2 MeSH
- Cytochrome P-450 CYP2E1 MeSH
- cytochrome P-450 CYP1A6 (fish) MeSH Browser
- indole-3-carbinol MeSH Browser
- Indoles MeSH
- Cytochrome P-450 CYP1A2 Inhibitors MeSH
- Cytochrome P-450 CYP2E1 Inhibitors MeSH
- Cytochrome P-450 Enzyme Inhibitors MeSH
- Oxindoles MeSH
- Skatole MeSH
- Cytochrome P-450 Enzyme System MeSH
OBJECTIVES: To study the contribution of individual purified porcine CYP1A2, 2E1 and 2A19 enzymes to the biotransformation of skatole. METHODS: Individual porcine and human enzymes (CYP1A2, 2E1 or 2A6/19) were used to study their potential involvement in skatole metabolism. Furthermore, the inhibition experiments using specific inhibitors of CYP1A2, 2E1 or 2A6/19, were performed. For determination of skatole biotransformation by individual CYP forms in reconstituted systems, HPLC method with UV detection was used. RESULTS: The data presented in this paper show that porcine and human CYPs are responsible for the formation of indole-3-carbinol and 3-methyloxindole. Whereas in pig CYP2A19 and CYP1A2 seem to be the most important for metabolism of skatole, in man CYP1A2 and CYP2E1 forms are mainly responsible for the production of the metabolites mentioned above. CONCLUSIONS: The porcine and human CYP1A2, 2E1, 2A6/19 forms contribute to formation of 3-methyloxindole and indole-3-carbinol.
Porcine cytochrome 2A19 and 2E1