RT Journal Article SR Electronic T1 Characterization of the Selectivity and Mechanism of Cytochrome P450 Inhibition by Dimethyl-4,4′-dimethoxy-5,6,5′,6′-
dimethylenedioxybiphenyl-2,2′-dicarboxylate JF Drug Metabolism and Disposition JO Drug Metab Dispos FD American Society for Pharmacology and Experimental Therapeutics SP 1555 OP 1560 VO 29 IS 12 A1 Ji-Yeon Kim A1 Minsun Baek A1 Sooyong Lee A1 Sung-Ok Kim A1 Mi-Sook Dong A1 Bok-Ryang Kim A1 Dong-Hyun Kim YR 2001 UL http://dmd.aspetjournals.org/content/29/12/1555.abstract AB In vitro studies with human liver microsomes and cytochrome P450 (P450) prototype substrates were performed to characterize the selectivity and mechanism of inhibition of P450 by dimethyl-4,4′-dimethoxy-5,6,5′,6′-dimethylenedioxybiphenyl-2,2′-dicarboxylate (DDB). DDB was found to be a strong inhibitor of testosterone 6β-hydroxylation activity (CYP3A4) with aKi value of 0.27 ± 0.21 μM. At higher concentrations, DDB marginally inhibited caffeineN3-demethylation (CYP1A2), diclofenac 4′-hydroxylation (CYP2C9), and dextromethorphanO-demethylation (CYP2D6) activities, but this compound had no effect on CYP2A6-, CYP2C19-, and CYP2E1-mediated reactions. Spectral analysis indicated that the formation of metabolite-P450 complex having absorbance at 456 nm was concentration-dependent; 5 to 33% of the total P450 was complexed in rat and human liver microsomes after a 5-min incubation with DDB. In addition, microsomal incubations with DDB in the presence of NADPH resulted in a loss of spectral P450 content, which was restored after adding K3Fe(CN)6. This complex formation resulted in a time-dependent loss of CYP3A-catalyzed marker activity (testosterone 6β-hydroxylation) in human liver microsomes. The inhibition was only partially restored upon dialysis. These results collectively suggest that formation of a metabolite-CYP3A complex with DDB was responsible for the CYP3A-selective time-dependent loss of catalytic function of CYP3A. The American Society for Pharmacology and Experimental Therapeutics