Modulation by neurosteroids of the in vivo (+)-[3H]SKF-10,047 binding to sigma 1 receptors in the mouse forebrain

J Neurosci Res. 1996 Dec 15;46(6):734-43. doi: 10.1002/(SICI)1097-4547(19961215)46:6<734::AID-JNR10>3.0.CO;2-U.

Abstract

Recent reports suggest an interaction between neuro-(active)steroids and sigma1 (sigma 1) receptors, affecting biochemical parameters as well as physiological responses mediated by sigma 1 ligands in the rodent brain. In this study, we examined the modulation by neurosteroids of the haloperidol-sensitive in vivo (+)-[3H]SKF-10,047 binding to sigma 1 sites in the mouse hippocampus and cortex. Progesterone (PROG; 2-40 mg/kg), pregnenolone sulfate (PREGS; 10-40 mg/kg), and dehydroepiandrosterone sulfate (DHEAS; 10-40 mg/kg) were administered systemically 10 min before the radioactive tracer. The total amount of (+)-[3H]SKF-10,047 bound in each structure was significantly affected by PROG and PREGS only at the highest dose tested and was unaffected by DHEAS. However, bound to free (B/F) radioactivity ratios were highly significantly decreased by 30-40% in each structure by PROG and PREGS. DHEAS, at 40 mg/kg, induced a significant 20% decrease in the hippocampus. Furthermore, the in vivo (+)-[3H]SKF-10,047 binding parameters were diminished in pregnant female mice compared to non-pregnant or male mice. These results confirm the in vitro binding results, bring a direct in vivo demonstration of the interaction between neurosteroids and sigma 1 receptors, and show that physiologic modulations of the steroidal concentrations affect the sigma 1 systems.

MeSH terms

  • Animals
  • Antipsychotic Agents / pharmacology*
  • Binding, Competitive / physiology
  • Cerebral Cortex / chemistry
  • Cerebral Cortex / metabolism
  • Dehydroepiandrosterone Sulfate / metabolism
  • Dehydroepiandrosterone Sulfate / pharmacology
  • Dose-Response Relationship, Drug
  • Female
  • Gonadal Steroid Hormones / metabolism
  • Gonadal Steroid Hormones / pharmacology*
  • Hippocampus / chemistry
  • Hippocampus / metabolism
  • Male
  • Mice
  • Phenazocine / analogs & derivatives*
  • Phenazocine / pharmacology
  • Pregnancy
  • Pregnenolone / metabolism
  • Pregnenolone / pharmacology
  • Progesterone / metabolism
  • Progesterone / pharmacology
  • Prosencephalon / chemistry*
  • Prosencephalon / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, sigma / metabolism*
  • Tritium

Substances

  • Antipsychotic Agents
  • Gonadal Steroid Hormones
  • Receptors, sigma
  • pregnenolone sulfate
  • Tritium
  • Progesterone
  • Dehydroepiandrosterone Sulfate
  • Pregnenolone
  • SK&F 10047
  • Phenazocine