Influence of Sulforaphane Metabolites on Activities of Human Drug-Metabolizing Cytochrome P450 and Determination of Sulforaphane in Human Liver Cells
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27779894
DOI
10.1089/jmf.2016.0063
Knihovny.cz E-zdroje
- Klíčová slova
- high performance liquid chromatography, inhibition, sulforaphane (cruciferous antioxidants),
- MeSH
- Brassica chemie MeSH
- cystein metabolismus MeSH
- cytochrom P-450 CYP2D6 účinky léků metabolismus MeSH
- glutathion metabolismus MeSH
- hepatocyty metabolismus MeSH
- inhibitory cytochromu P450 farmakologie MeSH
- isothiokyanatany analýza metabolismus farmakologie MeSH
- jaterní mikrozomy enzymologie MeSH
- játra chemie metabolismus MeSH
- lidé MeSH
- sulfoxidy MeSH
- systém (enzymů) cytochromů P-450 účinky léků metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cystein MeSH
- cytochrom P-450 CYP2D6 MeSH
- glutathion MeSH
- inhibitory cytochromu P450 MeSH
- isothiokyanatany MeSH
- sulforaphane MeSH Prohlížeč
- sulfoxidy MeSH
- systém (enzymů) cytochromů P-450 MeSH
The influence of metabolites of sulforaphane, natural compounds present in broccoli (Brassica oleracea var. botrytis italica) and in other cruciferous vegetables, on drug-metabolizing cytochrome P450 (CYP) enzymes in human liver microsomes and possible entry of sulforaphane into human hepatic cells were investigated. Metabolites studied are compounds derived from sulforaphane by the mercapturic acid pathway (conjugation with glutathione and by following reactions), namely sulforaphane glutathione and sulforaphane cysteine conjugates and sulforaphane-N-acetylcysteine. Their possible effect on four drug-metabolizing CYP enzymes, CYP3A4 (midazolam 1'-hydroxylation), CYP2D6 (bufuralol 1'-hydroxylation), CYP1A2 (7-ethoxyresorufin O-deethylation), and CYP2B6 (7-ethoxy-4-(trifluoromethyl)coumarin O-deethylation), was tested. Inhibition of four prototypical CYP activities by sulforaphane metabolites was studied in pooled human liver microsomes. Sulforaphane metabolites did not considerably affect biological function of drug-metabolizing CYPs in human liver microsomes except for CYP2D6, which was found to be inhibited down to 73-78% of the original activity. Analysis of the entry of sulforaphane into human hepatocytes was done by cell disruption by sonication, methylene chloride extraction, and modified high-performance liquid chromatography method. The results have shown penetration of sulforaphane into the human hepatic cells.
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