Metabolism of flavonolignans in human hepatocytes
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
29414024
DOI
10.1016/j.jpba.2018.01.048
PII: S0731-7085(17)32879-0
Knihovny.cz E-zdroje
- Klíčová slova
- Bactosomes, Cytochrome P450, Hepatocytes, LC/MS, Silybin, Silymarin,
- MeSH
- biotransformace fyziologie MeSH
- dospělí MeSH
- flavonolignany metabolismus MeSH
- hepatocyty metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- silibinin MeSH
- silymarin analogy a deriváty metabolismus MeSH
- systém (enzymů) cytochromů P-450 metabolismus MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- dehydrosilybin MeSH Prohlížeč
- flavonolignany MeSH
- isosilybin A MeSH Prohlížeč
- silibinin MeSH
- silymarin MeSH
- systém (enzymů) cytochromů P-450 MeSH
This study examined the in vitro biotransformation of eight structurally related flavonolignans, namely silybin, 2,3-dehydrosilybin, silychristin, 2,3-dehydrosilychristin, silydianin, 2,3-dehydrosilydianin, isosilybin A and isosilybin B. The metabolic transformations were performed using primary cultures of human hepatocytes and recombinant human cytochromes P450 (CYPs 1A2, 2A6, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1 and 3A4). The metabolites produced were analyzed by ultra-performance liquid chromatography coupled with tandem mass spectrometry. We found that each of the tested compounds was metabolized in vitro by one or more CYP enzymes, which catalyzed O-demethylation, hydroxylation, hydrogenation and dehydrogenation reactions. In human hepatocytes, silybin, 2,3-dehydrosilybin, silychristin, 2,3-dehydrosilychristin, and isosilybins A and B were directly conjugated by sulfation or glucuronidation. Moreover, isosilybin A was also converted to a methyl derivative, while isosilybin B was hydroxylated and methylated. Silydianin and 2,3-dehydrosilydianin were found to undergo hydrogenation and/or glucuronidation. In addition, 2,3-dehydrosilydianin was found to be metabolically the least stable flavonolignan in human hepatocytes, and its main metabolite was a cleavage product corresponding to a loss of CO. We conclude that the hepatic biotransformation of flavonolignans primarily involves the phase II conjugation reactions, however in some cases the phase I reactions may also occur. These results are highly relevant for research focused on flavonolignan metabolism and pharmacology.
Citace poskytuje Crossref.org
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