Recovery of Free Androgens in the Rat Prostate In Vivo and In Vitro after Treatment with Orally Active Testosterone Undecanoate (TU)

Summary

Short term castrated rats were sacrificed at different time intervals after oral administration of tritium labeled TU. Blood and organs were collected and measured for total radioactivity uptake. At the time of peak values of radioactivity the in vivo metabolite pattern was investigated by thin layer chromatography. In vitro studies were performed in plasma, muscle and prostate cytosol.

The radioactivity uptake into plasma and prostate in vivo reached a first maximum 2 1/2 h after oral administration of TU. A second peak appeared after 5 h in the prostate. While only 16 % of the total plasma radioactivity appeared in the non esterified fraction, the tissues contained 69-71 %. In plasma, the bulbocavernosus/levator ani muscle and in the skeletal muscle, free testosterone was the main unesterified androgen (14-28 %). Prostate and seminal vesicles contained primarily 5α-DHT (47 and 34 %, respectively). Further metabolites were found in the fractions of 17β-hydroxy-5α-androstanediols, epiandrosterone, androsterone, 4-androstenedione and 5α-androstanedione.

After incubation in vitro with TU, prostate and muscle cytosol contained significant amounts (39 % and 17 %, respectively) of free androgens.

It was concluded that peripheral organs as well as the prostate itself are capable of cleaving the undecanoic ester and that the biological action of TU is exerted by unesterified androgens which occur in a pattern similar to that obtained after i.v. injection of free testosterone.

Key-Words

Oral Androgen - Testosterone Undecanoate - Uptake and Metabolism - Rat Prostate