Interaction of luteolin, naringenin, and their sulfate and glucuronide conjugates with human serum albumin, cytochrome P450 (CYP2C9, CYP2C19, and CYP3A4) enzymes and organic anion transporting polypeptide (OATP1B1 and OATP2B1) transporters
Jazyk angličtina Země Francie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
36481402
DOI
10.1016/j.biopha.2022.114078
PII: S0753-3322(22)01467-6
Knihovny.cz E-zdroje
- Klíčová slova
- Cytochrome P450 enzymes, Human serum albumin, Luteolin, Naringenin, OATP transporters, Sulfate/glucuronide metabolites,
- MeSH
- cytochrom P-450 CYP3A * metabolismus MeSH
- cytochrom P450 CYP2C19 metabolismus MeSH
- cytochrom P450 CYP2C9 metabolismus MeSH
- flavonoidy farmakologie MeSH
- glukuronidy MeSH
- lidé MeSH
- lidský sérový albumin metabolismus MeSH
- luteolin farmakologie MeSH
- přenašeče organických aniontů * metabolismus MeSH
- sírany metabolismus MeSH
- systém (enzymů) cytochromů P-450 metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- CYP2C19 protein, human MeSH Prohlížeč
- CYP2C9 protein, human MeSH Prohlížeč
- CYP3A4 protein, human MeSH Prohlížeč
- cytochrom P-450 CYP3A * MeSH
- cytochrom P450 CYP2C19 MeSH
- cytochrom P450 CYP2C9 MeSH
- flavonoidy MeSH
- glukuronidy MeSH
- lidský sérový albumin MeSH
- luteolin MeSH
- přenašeče organických aniontů * MeSH
- sírany MeSH
- systém (enzymů) cytochromů P-450 MeSH
Luteolin and naringenin are flavonoids found in various foods/beverages and present in certain dietary supplements. After a high intake of these flavonoids, their sulfate and glucuronide conjugates reach micromolar concentrations in the bloodstream. Some pharmacokinetic interactions of luteolin and naringenin have been investigated in previous studies; however, only limited data are available in regard to their metabolites. In this study, we aimed to investigate the interactions of the sulfate and glucuronic acid conjugates of luteolin and naringenin with human serum albumin, cytochrome P450 (CYP2C9, 2C19, and 3A4) enzymes, and organic anion transporting polypeptide (OATP1B1 and OATP2B1) transporters. Our main findings are as follows: (1) Sulfate conjugates formed more stable complexes with albumin than the parent flavonoids. (2) Luteolin and naringenin conjugates showed no or only weak inhibitory action on the CYP enzymes examined. (3) Certain conjugates of luteolin and naringenin are potent inhibitors of OATP1B1 and/or OATP2B1 enzymes. (4) Conjugated metabolites of luteolin and naringenin may play an important role in the pharmacokinetic interactions of these flavonoids.
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