Inhibition of the CRF1 receptor influences the activity of antidepressant drugs in the forced swim test in rats

Naunyn Schmiedebergs Arch Pharmacol. 2017 Aug;390(8):769-774. doi: 10.1007/s00210-017-1377-0. Epub 2017 Apr 20.

Abstract

Hyperactivity of the hypothalamic-pituitary-adrenal axis (HPA) and impairment of the central corticotropin-releasing factor (CRF) system are factors in the pathogenesis of depression. Though several antagonists of the CRF1 receptor were effective in the recognized behavioral tests for antidepressant activity, there is still little information on the potential interactions between CRF1 receptor inhibitors and conventional antidepressant therapy. The aim of our study was to assess the influence of SN003, a CRF1 receptor blocker, on the activity of imipramine and fluoxetine in the forced swim test (FST) in rats which presented some signs of depression. The experiments were carried out on female Wistar rats subjected to 14-day subcutaneous corticosterone (CORT) administration (20 mg/kg/day). The antidepressant-like effect was determined by the FST and the CRF levels in the hypothalamus, amygdala, and peripheral blood were measured by a high-sensitivity immunoenzymatic test. SN003 (0.5 mg/kg) potentiated the antidepressant-like effect of imipramine (15 mg/kg) and fluoxetine (7.5 mg/kg). Moreover, the co-administration of the tested agents abolished CORT-induced increase in CRF levels in the examined biological material more profoundly than monotherapy. Our present findings give further evidence that the blockage of CRF action may be useful in the treatment of mood disorders. The concurrent use of well-known antidepressants with CRF1 receptor antagonists could be beneficial in terms of safety, since it requires lower doses of the applied agents.

Keywords: CRF1 receptor antagonist; Corticotropin-releasing factor level; Fluoxetine; Forced swim test; Imipramine; Rats.

MeSH terms

  • Amygdala / drug effects
  • Amygdala / metabolism
  • Animals
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use*
  • Behavior, Animal / drug effects
  • Corticosterone / pharmacology*
  • Corticotropin-Releasing Hormone / blood
  • Corticotropin-Releasing Hormone / metabolism
  • Depression / drug therapy*
  • Depression / metabolism
  • Drug Therapy, Combination
  • Female
  • Fluoxetine / pharmacology
  • Fluoxetine / therapeutic use
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Imipramine / pharmacology
  • Imipramine / therapeutic use
  • Locomotion / drug effects
  • Pyridines / pharmacology
  • Pyridines / therapeutic use
  • Rats, Wistar
  • Receptors, Corticotropin-Releasing Hormone / antagonists & inhibitors*
  • Receptors, Corticotropin-Releasing Hormone / metabolism
  • Swimming
  • Triazoles / pharmacology
  • Triazoles / therapeutic use

Substances

  • Antidepressive Agents
  • Pyridines
  • Receptors, Corticotropin-Releasing Hormone
  • SN003
  • Triazoles
  • Fluoxetine
  • CRF receptor type 1
  • Corticotropin-Releasing Hormone
  • Imipramine
  • Corticosterone