Ethinylestradiol interacts with liver microsomes and induces binding sites for steroid hormones in the male rat liver

J Pharmacol Exp Ther. 1994 Sep;270(3):1121-6.

Abstract

The present work focuses on the interaction of 17 alpha-ethinyl estrogen derivatives with the [3H]dexamethasone ([3H]DEX) binding site from male rat liver microsomes and the induction of this site by the in vivo administration of natural and synthetic estrogens. [3H]DEX binds to a single-saturating binding site (Kd = 100 nM; maximal binding = 13 pmol/mg of protein) in the liver microsomes. In competition experiments, ethinylestradiol (EE2) and mestranol were able to inhibit [3H]DEX binding to microsomes, whereas natural estrogens, tamoxifen or estrogen sulfates were ineffective. Saturation analysis performed by incubating [3H]EE2 with liver microsomes revealed the existence of a low-affinity (Kd = 280 +/- 30 nM) and high capacity (maximal binding = 16 +/- 2 pmol/mg of protein) binding site. Saturation, competition and dissociation experiments suggest that [3H]DEX and [3H]EE2 interact with the same microsomal entity. Synthetic and natural estrogens increased the hepatic expression of the [3H]DEX binding site in immature, hypothyroid and hypophysectomized male rats. This induction required at least 2 days of treatment, and could only be achieved by pharmacological doses of estrogens.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites / drug effects
  • Dexamethasone / metabolism*
  • Dose-Response Relationship, Drug
  • Estrogens / pharmacology
  • Ethinyl Estradiol / pharmacology*
  • Hypophysectomy
  • Hypothyroidism / metabolism
  • Kinetics
  • Male
  • Microsomes, Liver / drug effects*
  • Microsomes, Liver / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Estrogens
  • Ethinyl Estradiol
  • Dexamethasone