THE INHIBITION OF HUMAN PROSTATIC AROMATASE-ACTIVITY BY IMIDAZOLE DRUGS INCLUDING KETOCONAZOLE AND 4-HYDROXYANDROSTENEDIONE

Ketoconazole, an orally active imidazole drug and bifonazole, clotrimazole, econazole, isoconazole, miconazole and tioconazole are known as inhibitors of cytochrome P450 dependent steroidogenic enzymes including human placental aromatase. The aim of the present study was to investigate the effectiveness of these imidazole drugs to inhibit human prostatic aromatase activity compared with the known inhibitor of aromatase 4-hydroxyandrostenedione (4-OHA). The imidazole drugs and 4-OHA inhibited prostatic aromatase activity in a dose-dependent manner. The order of decreasing inhibitory potency determined from IC50 values μmol/L) was: 4-OHA (1.57) > bifonazole (1.6) > tioconazole (1.69) > clotrimazole (1.73) > econazole (1.87) > miconazole (2.0) > isoconazole (2.2) > ketoconazole (4.7). The ic50 values for the inhibition of prostatic homogenate aromatase activity are 3-9-fold higher than that for the inhibition of human placental aromatase activity, previously reported, except that of ketoconazole which was 1.5-fold lower than that for the inhibition of placental microsomal aromatase. © 1990.