Sandrini M, Vergoni A V, Bertolini A
Istituto di Farmacologia, Università di Modena, Italy.
J Endocrinol Invest. 1993 Oct;16(9):679-81. doi: 10.1007/BF03348909.
In intact adult male rats an inhibitor of aromatase and an inhibitor of 5 alpha-reductase did not change the characteristics of [3H]imipramine binding sites in cerebral cortex, hypothalamus, and hippocampus. Testosterone, estradiol and dihydrotestosterone prevented the effect of castration on the number of [3H]imipramine binding sites, but had no effect in non-castrated animals. These data suggest that testosterone and its major metabolites, estradiol and dihydrotestosterone, are equally effective with regard to imipramine binding sites.