RT Journal Article SR Electronic T1 The Role of CYP2C19 in the Metabolism of (+/−) Bufuralol, the Prototypic Substrate of CYP2D6 JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP 1024 OP 1028 VO 27 IS 9 A1 Mankowski, Dayna C. YR 1999 UL http://dmd.aspetjournals.org/content/27/9/1024.abstract AB Upon characterization of baculovirus-expressed cytochrome P-450 (CYP) 2C19, it was observed that this enzyme metabolized (+/−) bufuralol to 1′hydroxybufuralol, a reaction previously understood to be selectively catalyzed by CYP2D6. The apparentKm for this reaction was 36 μM with recombinant CYP2C19, approximately 7-fold higher than for recombinant CYP2D6. The intrinsic clearance for this reaction was 37-fold higher with CYP2D6 than for CYP2C19. The involvement of human CYP1A2 in bufuralol 1′-hydroxylation was also confirmed using the recombinant enzyme. Using S-mephenytoin as an inhibitor, theKi for inhibition of recombinant CYP2C19-mediated bufuralol hydroxylation was 42 μM, which is the approximate Km for recombinant CYP2C19-mediated S-mephenytoin metabolism. The classic CYP2D6 inhibitors quinidine and quinine showed no inhibition of CYP2C19-catalyzed bufuralol metabolism at concentrations that abolished CYP2D6-mediated bufuralol metabolism. Ticlopidine, a potent inhibitor of CYP2C19 and CYP2D6, inhibited bufuralol 1′-hydroxylation by each of these enzymes equipotently. In human liver microsomes that are known to be deficient in CYP2D6 activity, it was shown that in the presence of quinidine, the Km shifted from 14 to 38 μM. This is consistent with the Kmdetermination for recombinant CYP2C19 of 36 μM. In human liver microsomes that have high CYP2D6 and CYP2C19 activity, theKm shifted to 145 μM in the presence ofS-mephenytoin and quinidine, consistent with theKm determined for CYP1A2. This data suggests that bufuralol, and possibly other CYP2D6 substrates, have the potential to be metabolized by CYP2C19. The American Society for Pharmacology and Experimental Therapeutics