In vitro study of rat prostate 5 alpha-reductase activity and its inhibition

Int Urol Nephrol. 1992;24(2):145-54. doi: 10.1007/BF02549642.

Abstract

A simple and rapid method of measuring 5 alpha-reductase (5 alpha-R) activity and of determining the kinetic parameters (KM and Vmax) of the enzyme is described. The 5 alpha-R activity in the homogenate of the prostate of Wistar rats aged 8-12 weeks was established, and the effects of natural and synthetic steroids and of non-steroidal antiandrogens (IC50) upon the 5 alpha-R activity were studied. Of the natural steroids, 17-OH-progesterone was found to have the highest inhibitory effect (IC50 = 1.35 microM), followed in decreasing order by progesterone (IC50 = 5.0 microM) and 4-androstene-3,17-dione (IC50 = 21.6 microM). Oestradiol-17 beta had practically no inhibitory effect. Of the synthetic steroids, 4-MA had the highest inhibitory effect (IC50 = 0.068 microM), followed by nortestosterone (IC50 = 7.4 microM) and RU-486 (Mifepristone) (IC50 = 115 microM). Even at 1000 microM, cyproterone acetate exerted no inhibitory effect. Of the nonsteroidal compounds, ketoconazole proved a weak inhibitor (IC50 = 115 microM), while flutamide was practically ineffective.

MeSH terms

  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / metabolism*
  • 5-alpha Reductase Inhibitors*
  • Androgen Antagonists / pharmacology
  • Animals
  • Hormones / pharmacology
  • In Vitro Techniques
  • Male
  • Prostate / enzymology*
  • Rats
  • Rats, Inbred Strains

Substances

  • 5-alpha Reductase Inhibitors
  • Androgen Antagonists
  • Hormones
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase