Can bioactive compounds of Crocus sativus L. influence the metabolic activity of selected CYP enzymes in the rat?
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26681074
DOI
10.33549/physiolres.933203
PII: 933203
Knihovny.cz E-zdroje
- MeSH
- aktivace enzymů účinky léků fyziologie MeSH
- Crocus * MeSH
- cyklohexeny izolace a purifikace farmakologie MeSH
- jaterní mikrozomy účinky léků enzymologie MeSH
- karotenoidy izolace a purifikace farmakologie MeSH
- krysa rodu Rattus MeSH
- potkani Wistar MeSH
- rostlinné extrakty izolace a purifikace farmakologie MeSH
- systém (enzymů) cytochromů P-450 metabolismus MeSH
- terpeny izolace a purifikace farmakologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- crocin MeSH Prohlížeč
- cyklohexeny MeSH
- karotenoidy MeSH
- rostlinné extrakty MeSH
- safranal MeSH Prohlížeč
- systém (enzymů) cytochromů P-450 MeSH
- terpeny MeSH
Safranal and crocin are biologically active compounds isolated from Crocus sativus L., commonly known as saffron. Clinical trials confirm that saffron has antidepressant effect, thus being a potential valuable alternative in the treatment of depression. The aim of the present study was to determine, whether systemic administration of safranal and crocin can influence the metabolic activity of CYP3A, CYP2C11, CYP2B, and CYP2A in rat liver microsomes (RLM). The experiments were carried out on male Wistar albino rats intragastrically administered with safranal (4, 20, and 100 mg/kg/day) or with intraperitoneal injections of crocin (4, 20, and 100 mg/kg/day). Our results demonstrate the ability of safranal and crocin to increase the total protein content and to change the metabolic activity of several CYP enzymes assessed as CYP specific hydroxylations of testosterone in RLM. Crocin significantly decreased the metabolic activity of all selected CYP enzymes, while safranal significantly increased the metabolic activity of CYP2B, CYP2C11 and CYP3A enzymes. Therefore, both substances could increase the risk of interactions with co-administered substances metabolized by cytochrome P450 enzymes.
Citace poskytuje Crossref.org
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