Membrane mechanism mediates progesterone stimulatory effect on LHRH release from superfused rat hypothalami in vitro

Neuroendocrinology. 1987 Jun;45(6):514-7. doi: 10.1159/000124784.

Abstract

To determine whether the plasma membrane is a primary site for progesterone (P4) action on the neural LHRH apparatus of hypothalamic tissues derived from ovariectomized, estradiol-primed (OVX + E2) immature rats, immobilized P4 was infused directly to these tissues using a superfusion technique. Two kinds of immobilized P4 with bovine serum albumin (BSA) conjugated at positions 3 or 11, or 11-deoxycorticosterone (DOC) immobilized at position 21 of the steroid molecule, respectively, were tested for structural specificity. Among the three immobilized steroids, only P4 with BSA conjugated at position 3 (P4-3-BSA) was effective in stimulating LHRH release in vitro. P4-3-BSA at 0.5 micrograms/ml, approximately 1.7 X 10(-7) M of P4, increased LHRH levels in the superfusates to about 2.5-fold those of pretreatment levels. In addition, no conversion of P4-3-BSA to free progesterone was detected. This observation demonstrated that the plasma membrane is a primary site for the stimulating effect of P4 on LHRH release from hypothalamic tissue in vitro.

Publication types

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

MeSH terms

  • Animals
  • Cell Membrane / physiology
  • Drug Implants
  • Estradiol / pharmacology
  • Female
  • Gonadotropin-Releasing Hormone / metabolism*
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism*
  • In Vitro Techniques
  • Kinetics
  • Ovariectomy
  • Progesterone / pharmacology*
  • Rats

Substances

  • Drug Implants
  • Gonadotropin-Releasing Hormone
  • Progesterone
  • Estradiol