Abstract

Recombinant cytochrome P450 phenotyping, different approaches for estimating fraction metabolized (f_m), and multiple measures of in vivo inhibitor exposure were tested for their ability to predict drug interaction magnitude in dogs. Previously, midazolam-ketoconazole interaction studies in dogs have been attributed to inhibition of CYP3A pathways. However, in vitro phenotyping studies demonstrated higher intrinsic clearances (CL_int,app) of midazolam with canine CYP2B11 and CYP2C21. Application of activity correction factors and isoform hepatic abundance to liver microsome CL_int,app values further implicated CYP2B11 (f_m≥0.89) as the dog enzyme responsible for midazolam- and temazepam-ketoconazole interactions in vivo. Mean AUCi/AUC ratios from intravenous and oral midazolam interaction studies were predicted well with unbound K_i and estimates of unbound hepatic inlet inhibitor concentrations and intestinal metabolism using the AUC-competitive inhibitor relationship. No interactions were observed in vivo with bufuralol, although significant interactions with bufuralol were predicted with fluoxetine via CYP2D and CYP2C pathways (>2.45-fold) but not with clomipramine (<2-fold). The minor caffeine-fluvoxamine interaction (1.78-fold) was slightly higher than predicted values based on determination of a moderate f_m value for CYP1A1, although CYP1A2 may also be involved in caffeine metabolism. The findings suggest promise for in vitro approaches to drug interaction assessment in dogs, but also highlight the need to identify improved substrate and inhibitor probes for canine P450s.