PT - JOURNAL ARTICLE AU - Regina W. Wang AU - Deborah J. Newton AU - Tad D. Scheri AU - Anthony Y. H. Lu TI - Human Cytochrome P450 3A4-Catalyzed Testosterone 6β-Hydroxylation and Erythromycin<em>N</em>-Demethylation DP - 1997 Apr 01 TA - Drug Metabolism and Disposition PG - 502--507 VI - 25 IP - 4 4099 - http://dmd.aspetjournals.org/content/25/4/502.short 4100 - http://dmd.aspetjournals.org/content/25/4/502.full SO - Drug Metab Dispos1997 Apr 01; 25 AB - Cytochrome P450 3A4 is known to catalyze the metabolism of both endogenous substrates (such as the 6β-hydroxylation of testosterone) and many important therapeutic agents, including theN-demethylation of erythromycin. However, erythromycin and testosterone have been reported to have little or no effect on the metabolism of each other by recombinant CYP3A4. In an effort to understand the basis of these observations, we studied theN-demethylation of erythromycin and the 6β-hydroxylation of testosterone in human liver microsomes and in microsomes from cells containing recombinant human CYP3A4 and P450 reductase under a variety of experimental conditions. In both human liver microsomal and recombinant CYP3A4 systems, erythromycin inhibited testosterone 6β-hydroxylation in a concentration dependent manner, and vice versa. However, the inhibition mechanism was complex. At low substrate concentrations, testosterone and erythromycin acted as competitive inhibitors to each other. Under these experimental conditions, an apparent competitive inhibition of testosterone 6β-hydroxylation by erythromycin was observed, withKi values similar to that of theKm values for erythromycin. When the rates of testosterone 6β-hydroxylation and erythromycinN-demethylation were determined in microsomal incubations containing both substrates at lower concentrations, the observed rates for each reaction were in good agreement with the calculated rates based on the rate equation describing simultaneous metabolism of two substrates by a single enzyme. However, at high substrate concentrations, the kinetic results could be best explained by a mechanism involving partial competitive inhibition. We conclude from these studies that testosterone and erythromycin mutually inhibit the metabolism of each other, consistent with the fact that CYP 3A4 catalyzes the metabolism of both substrates. The American Society for Pharmacology and Experimental Therapeutics