Time-dependent effects of ovarian steroids on tyrosine hydroxylase activity in the limbic forebrain of female rats

J Neural Transm Gen Sect. 1991;83(1-2):77-84. doi: 10.1007/BF01244454.

Abstract

In this work, we have studied the time-course of the effects of pharmacological administration of ovarian steroids on tyrosine hydroxylase (TH) activity in the limbic forebrain of ovariectomized rats. Administration of estradiol produced a late decrease in TH activity. This effect was found 24 hours after the last steroid injection, disappearing at 32 hours. It was antagonized by progesterone, since a single injection of this steroid to estradiol-pretreated rats reversed to control values the estradiol-induced decrease. Nevertheless, the administration of progesterone after estradiol treatment caused a short-time decrease in the limbic activity of TH, which was observed 4 hours after the last steroid injection, disappearing subsequently. On the other hand, the administration of progesterone alone produced a biphasic effect, with a reduction at 24 hours, followed by an increase at 32 hours. These effects were only observed in the animals non-treated with estradiol, disappearing with a previous treatment with estrogens. Hence, it can be concluded that both ovarian steroids may affect the limbic TH activity. Thus, estradiol produced a late inhibitory effect on the activity of this enzyme, which was antagonized by progesterone. Administration of the last one to estradiol-treated rats produced a short-time inhibitory effect, whereas its administration to non-treated rats produced a late biphasic effect (inhibition followed by stimulation), which was not observed in estradiol-treated rats.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dopamine / metabolism
  • Drug Interactions
  • Enzyme Induction / drug effects
  • Estradiol / pharmacology*
  • Female
  • Limbic System / drug effects*
  • Limbic System / enzymology
  • Ovariectomy
  • Progesterone / pharmacology*
  • Rats
  • Time Factors
  • Tyrosine 3-Monooxygenase / antagonists & inhibitors*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Progesterone
  • Estradiol
  • Tyrosine 3-Monooxygenase
  • Dopamine