Unexpected virilization in male mice lacking steroid 5 alpha-reductase enzymes

Endocrinology. 2001 Nov;142(11):4652-62. doi: 10.1210/endo.142.11.8510.

Abstract

Mice lacking steroid 5 alpha-reductase 1 and 2 were produced by gene targeting and breeding. Male mice without 5 alpha-reductase 2 or without both enzymes had fully formed internal and external genitalia and were fertile, but had smaller prostates and seminal vesicles than controls. T accumulated to high levels in the reproductive tissues of the mutant mice. DHT administration increased seminal vesicle and coagulating gland weights in mice deficient in 5 alpha-reductase 2 and increased the weights of the prostate, seminal vesicle, and coagulating gland in animals deficient in both enzymes. An inhibitor of both 5 alpha-reductases (GI 208335X) decreased prostate and coagulating gland weights of control mice, but had no effect in those lacking 5 alpha-reductase 1 and 2. Castration reduced the sizes of these tissues in animals of all genotypes. Androgen-dependent gene expression was decreased in the seminal vesicles of mice lacking one or more 5 alpha-reductases and was restored by administration of T or DHT. Female mice missing both enzymes exhibited parturition and fecundity defects similar to those of animals without 5 alpha-reductase 1. We conclude that T is the only androgen required for differentiation of the male urogenital tract in mice and that the synthesis of DHT serves largely as a signal amplification mechanism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / deficiency*
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / genetics
  • 5-alpha Reductase Inhibitors
  • Androgens / physiology
  • Androstenes / pharmacology
  • Animals
  • Dihydrotestosterone / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Female
  • Fertility
  • Genitalia, Male / drug effects
  • Genitalia, Male / growth & development
  • Genitalia, Male / metabolism
  • Genitalia, Male / pathology
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / deficiency*
  • Isoenzymes / genetics
  • Male
  • Mice
  • Mice, Knockout / genetics
  • Mutation / physiology
  • Phenotype
  • RNA, Messenger / metabolism
  • Reference Values
  • Testosterone / metabolism
  • Virilism / enzymology*
  • Virilism / pathology

Substances

  • 5-alpha Reductase Inhibitors
  • Androgens
  • Androstenes
  • Enzyme Inhibitors
  • Isoenzymes
  • N-(1-(4-trifluoromethylphenyl)cyclopentenyl)-3-oxo-4-aza-5a-androst-1-ene-17beta-carboxamide
  • RNA, Messenger
  • Dihydrotestosterone
  • Testosterone
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase