Abstract

Progesterone and its derivatives exert their antiandrogenic action by competing with testosterone for the active site of the 5c~-reductase enzyme [1-3]. The potential clinical value of this class of steroidal compounds in the treatment of androgen-related cutaneous disorders is well recognized. Byrnes et al. [4] showed 30 years ago that 11c~-hydroxyprogesterone (11 c~OHP), a synthetic derivative of progesterone, possesses antiandrogenic activity with minimal estrogenic and progestational side effects. Recently, Tamm et al. [5] claimed that 11 ~-OHP significantly reduces sebum production in men and women after 2 weeks of topical therapy. In order to confirm their results, we tested the effects of 11 c~-OHP on the flank-organ and ear sebaceous glands of adult male Syrian golden hamsters. These structures are considered to be reliable bioassay systems for the study of topically applied androgens and antiandrogens [ 6 9]. The materials and the methods used in this report have been previously described in more detail [10]. Progesterone and llc~-OHP (Upjohn, Kalamazoo, MI, USA) were dissolved in acetone at a concentration of 2.5 %. Fifty microliters of each solution was applied daily (except weekends) on the right flank organ, once in the morning and once in the afternoon. This regimen corresponded to a topical dose of 2.5 rag/day for a total of 4 weeks (Experiment 1). Control animals received topical applications of 50 #1 of acetone alone. Table 1 (Experiment 1) demonstrates that l l e O H P did not show any effects. In contrast, progesterone showed a 40 % reduction in the area of flank-organ pigmentation.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call