Porcine CYP2A19, CYP2E1 and CYP1A2 forms are responsible for skatole biotransformation in the reconstituted system
Jazyk angličtina Země Švédsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20027142
PII: NEL300709A05
Knihovny.cz E-zdroje
- MeSH
- cytochrom P-450 CYP1A2 metabolismus MeSH
- cytochrom P-450 CYP2E1 metabolismus MeSH
- indoly metabolismus MeSH
- inhibitory cytochromu P450 CYP1A2 MeSH
- inhibitory cytochromu P450 CYP2E1 MeSH
- inhibitory cytochromu P450 MeSH
- lidé MeSH
- oxindoly MeSH
- prasata MeSH
- skatol metabolismus MeSH
- systém (enzymů) cytochromů P-450 metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 3-methyloxindole MeSH Prohlížeč
- cytochrom P-450 CYP1A2 MeSH
- cytochrom P-450 CYP2E1 MeSH
- cytochrome P-450 CYP1A6 (fish) MeSH Prohlížeč
- indole-3-carbinol MeSH Prohlížeč
- indoly MeSH
- inhibitory cytochromu P450 CYP1A2 MeSH
- inhibitory cytochromu P450 CYP2E1 MeSH
- inhibitory cytochromu P450 MeSH
- oxindoly MeSH
- skatol MeSH
- systém (enzymů) cytochromů P-450 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