Metabolism of ropinirole is mediated by several canine CYP enzymes.
Autor: | Tervahauta T; Orion Corporation, Orion Pharma, Espoo, Finland., Uutela P; Orion Corporation, Orion Pharma, Espoo, Finland., Koskinen M; Orion Corporation, Orion Pharma, Espoo, Finland. |
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Jazyk: | angličtina |
Zdroj: | Veterinary medicine and science [Vet Med Sci] 2023 Jul; Vol. 9 (4), pp. 1584-1591. Date of Electronic Publication: 2023 Jun 15. |
DOI: | 10.1002/vms3.1188 |
Abstrakt: | Background: Ropinirole has been shown to provoke vomiting in dogs by activating the dopamine D2-like receptors in the chemoreceptor trigger zone. In humans, ropinirole is metabolized primarily by CYP1A2. Corresponding dog CYP1A2 is known to be a polymorphic enzyme which can cause variation in pharmacokinetics of compounds metabolised via this enzyme. Objectives: The aim of this study was to understand metabolic clearance of ropinirole in dogs, the enzymes involved in ropinirole metabolism and specially to estimate whether the clearance can be sensitive towards the polymorphism of canine CYP1A2. Methods: Metabolism of ropinirole was studied in dog hepatocytes and specific recombinant canine CYP isoforms. Metabolite identification and metabolite formation were evaluated using LC-mass spectrometry. Results: Ropinirole was moderately stable in dog hepatocytes with Cl Conclusions: Although human metabolism of ropinirole is mainly mediated through CYP1A2, the current study shows that several canine CYP isoforms are able to contribute to the clearance of ropinirole in dogs. This is expected to reduce a possible impact of canine CYP1A2 polymorphism on ropinirole pharmacokinetics. (© 2023 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.) |
Databáze: | MEDLINE |
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