Inhibition study of human placental aromatase with 3-deoxy- and 6-oxo-steroids using [1 beta-3H]16 alpha-hydroxyandrostenedione as a substrate: a comparison to that using [1 beta-3H]androstenedione.

Inhibition of aromatase activity in human placental microsomes with 3-deoxy- (1, 2, 4, 6 and 8), 6-oxo- (3, 5 and 9), and 16 alpha-bromo- (7) steroids was studied using [1 beta-3H]16 alpha-hydroxyandrostenedione (16 alpha-OHAD) as a substrate and compared to that with the conventional substrate, [1 beta-3H]androstenedione. All the steroids inhibited both 16 alpha-OHAD and [1 beta-3H]androstenedione aromatization in a competitive manner. Based on Ki/Km ratios obtained in both series of experiments, their relative inhibitory activities in the series with 16 alpha-OHAD were not necessarily identical with those in the other series. The results would be important to understand the relationship of structure to function of aromatase in human placental microsomes.