Effect of oral co-administration of frozen-dried grapefruit juice on pharmacokinetics of tramadol in dogs

Document Type: Full paper (Original article)

Authors

1 Veterinary Teaching Hospital 24 h, Department of Veterinary Clinics, University of Pisa, Via Livornese (lato monte) 1 San Piero a Grado, 56010 Pisa, Italy

2 Veterinary Teaching Hospital 24 h, Department of Veterinary Clinics, University of Pisa, Via Livornese (lato monte) 1 San Piero a Grado, 56010 Pisa, Italy; Department of Pharmaceutical Sciences, Via Bonanno 6, 56126 Pisa, Italy

3 Department of Pharmaceutical Sciences, Via Bonanno 6, 56126 Pisa, Italy

4 Institute of Veterinary Science, College of Veterinary Medicine, Chungnam National University, Daejeon 305-764, South Korea

5 Department of Pharmaceutical Sciences, Via Bonanno 6, 56126 Pisa, Italy;

Abstract

Tramadol is a centrally acting analgesic drug extensively metabolized in animal species. Its clinical
response is mainly due to the M1 metabolite, poorly produced in dogs. Grapefruit-juice can inhibit the
metabolism of different drugs in animals and humans. The aim of the present study was to evaluate the
pharmacokinetics of tramadol and its major metabolites after co-administration of tramadol and frozen-dried grapefruit-juice. A balanced cross-over study was used involving six male Beagle dogs. They were administered with tramadol alone (5 mg/kg) or with tramadol (5 mg/kg) plus frozen-dried grapefruit-juice (10 g). The plasma concentration vs time curves showed significant differences during the first 4 h following drug administration. Tmax was at 1.33 and 1.70 h following tramadol and tramadol plus frozen-dried grapefruit-juice treatment, respectively. Significant differences were also shown in Cmax (490 vs 270 ng/ml) and AUC (11,610 vs 5,890 h·h·ng/ml). Significant differences between the treatments were shown in all the M1 parameters reported. M2 and M5 did not show significant differences after both administrations. In conclusion, the frozen-dried grapefruit-juice was shown to affect the plasma concentrations of M1, despite them being well below those reported in humans.

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