Pharmacokinetics of a single oral dose of grapiprant in juvenile pigs (Sus scrofa domestica)

Author:

Kleine Stephanie1ORCID,Hampton Chiara E.2,Smith Christopher1,Bussieres Genevieve1,Mulon Pierre‐Yves2,Seddighi Reza2,Cox Sherry3,Smith Joe2

Affiliation:

1. Department of Small Animal Clinical Sciences, College of Veterinary Medicine University of Tennessee Knoxville Tennessee USA

2. Department of Large Animal Clinical Sciences, College of Veterinary Medicine University of Tennessee Knoxville Tennessee USA

3. Department of Biomedical and Diagnostic Sciences, College of Veterinary Medicine University of Tennessee Knoxville Tennessee USA

Abstract

AbstractBoth pet and research pigs can suffer from some degree of pain from surgery, injuries, or osteoarthritis (OA). Despite this, there is a paucity of data on safe and effective analgesia agents in pigs. Grapiprant is an EP4 antagonist that blocks the action of the pro‐inflammatory prostanoid, PGE2. It has shown efficacy in attenuating pain associated with ovariohysterectomy and OA in dogs. However, there are no data regarding grapiprant in pigs. Therefore, the pharmacokinetic profile of orally administered grapiprant to juvenile pigs (Sus scrofa domestica) was evaluated in this study. Seven juvenile pigs received 12 mg/kg grapiprant orally. Blood was collected from an indwelling jugular catheter using the push–pull method at set timepoints up to 48 hours. Sample analysis was performed with high‐performance liquid chromatography. Mean grapiprant plasma concentration was 164.3 ± 104.7 ng/mL which occurred at 0.8 ± 0.3 h. This study demonstrated that grapiprant concentrations consistent with analgesia in dogs were reached at this dosage in pigs. Further studies are needed to evaluate the efficacy of grapiprant in pigs.

Funder

University of Tennessee, Knoxville

Publisher

Wiley

Subject

General Veterinary,Pharmacology

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