Comparison of biotransformation and efficacy of aminoacetonitrile anthelmintics in vitro
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
25922167
DOI
10.1002/dta.1806
Knihovny.cz E-zdroje
- Klíčová slova
- drug metabolism, hepatocytes, micro-agar larval development test, monepantel, structure-metabolism relationships,
- MeSH
- aminoacetonitrily analogy a deriváty analýza farmakokinetika toxicita MeSH
- anthelmintika analýza farmakokinetika toxicita MeSH
- biotransformace MeSH
- Haemonchus účinky léků MeSH
- hepatocyty metabolismus MeSH
- krysa rodu Rattus MeSH
- kultivované buňky MeSH
- larva MeSH
- mebendazol analogy a deriváty analýza farmakokinetika MeSH
- ovce MeSH
- potkani Wistar MeSH
- tandemová hmotnostní spektrometrie MeSH
- thiabendazol analýza farmakokinetika MeSH
- vysokoúčinná kapalinová chromatografie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- aminoacetonitrily MeSH
- anthelmintika MeSH
- flubendazole MeSH Prohlížeč
- mebendazol MeSH
- monepantel MeSH Prohlížeč
- thiabendazol MeSH
The present in vitro study was designed to test and compare anthelmintic activity, hepatotoxicity, and biotransformation of four selected aminoacetonitrile derivatives (AADs): monepantel (MOP, anthelmintic approved for the treatment), AAD-970, AAD-1154, and AAD-1336. Micro-agar larval development test, MTT test of cytotoxicity, and biotransformation study coupled with Ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) technique were used for this purpose. Larvae of two Haemonchus contortus strains (drug susceptible and multi-drug resistant) and primary cultures of rat and ovine hepatocytes served as model systems. All AADs (including MOP) exhibited significant larvicidal effect in H. contortus susceptible as well as multi-resistant strains, much higher than those of reference anthelmintics thiabendazole and flubendazole. AAD-1154 provides the best results for most tested parameters among all AADs in this study. The cytotoxicity test showed that all AADs can be considered as nontoxic for hepatocytes. In the biotransformation study, Phase I and Phase II metabolites of AADs were identified and schemes of possible metabolic pathways in ovine hepatocytes were proposed. Biotransformation of MOP was much more extensive than biotransformation of other AADs. Based on obtained results, AAD-1154 and AAD-1336 can be considered as promising candidates for further in vivo testing.
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