Monepantel induces hepatic cytochromes p450 in sheep in vitro and in vivo
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25555458
DOI
10.1016/j.cbi.2014.12.025
PII: S0009-2797(14)00410-4
Knihovny.cz E-zdroje
- Klíčová slova
- Anthelmintics, CYP3A, CYP3A24, Drug–drug interactions, Zolvix,
- MeSH
- aminoacetonitrily analogy a deriváty farmakologie MeSH
- cytochrom P-450 CYP3A genetika metabolismus MeSH
- hepatocyty cytologie účinky léků enzymologie MeSH
- játra účinky léků enzymologie MeSH
- kultivované buňky MeSH
- messenger RNA metabolismus MeSH
- ovce MeSH
- protein - isoformy genetika metabolismus MeSH
- systém (enzymů) cytochromů P-450 genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- aminoacetonitrily MeSH
- cytochrom P-450 CYP3A MeSH
- messenger RNA MeSH
- monepantel MeSH Prohlížeč
- protein - isoformy MeSH
- systém (enzymů) cytochromů P-450 MeSH
Monepantel (MOP), a new amino-acetonitrile anthelmintic for the treatment and control of gastrointestinal nematode infections and associated diseases in sheep, is approved and marketed as oral solution under the trade name Zolvix® (Novartis Animal Health Inc., Switzerland). The effect of MOP on hepatic cytochromes P450 (CYP) has been investigated in sheep. In an in vivo experiment, castrated rams (9-months old) were treated with the recommended therapeutic dose of MOP. Non-treated animals represented the controls. After 24 h, the animals were stunned and exsanguinated. Microsomal fractions and total RNA were prepared from liver homogenates. The activities towards alkyloxyresorufins, 7-methoxy-4-trifluoromethylcoumarin and midazolam were assayed and mRNAs of individual CYP isoforms were quantified. In an in vitro procedure, primary cultures of ovine hepatocytes were incubated with or without MOP (10 μM) for 24 h and then expression levels of individual CYP isoforms were analyzed. Results showed that MOP significantly increased all CYP-related activities and CYP3A24 mRNA in sheep. The induction effect of MOP on CYP3A was similar or even higher than those of dexamethasone and rifampicin, well-known CYP3A inducers. As CYP3A enzymes belongs to the most important biotransformation enzymes, their induction may have serious pharmacological and/or toxicological consequences. These facts should be taken into account when other drugs together with or after MOP (Zolvix®) are administered to sheep.
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