Effects of the selective nonpeptide corticotropin-releasing factor receptor 1 antagonist antalarmin in the chronic mild stress model of depression in mice

Prog Neuropsychopharmacol Biol Psychiatry. 2003 Jun;27(4):625-31. doi: 10.1016/S0278-5846(03)00051-4.

Abstract

Several recent studies on corticotropin-releasing factor (CRF) have suggested that this neuropeptide may play a role in depression. Consequently, CRF receptor antagonists have been proposed as potential new agents for the treatment of this condition. This study investigated the effects of a 4-week treatment with the well-known CRF(1) receptor antagonist, antalarmin, and the prototypical selective serotonin reuptake inhibitor (SSRI), fluoxetine, in the chronic mild stress (CMS) model in BALB/c mice. Animals were exposed to 9 weeks of CMS which rapidly (within 2 weeks) produced decrease of physical state (PS), body weight gain and blunted emotional response in the light/dark test. Chronic treatment with antalarmin (10 mg/kg ip) and fluoxetine (10 mg/kg ip) led to an improvement of CMS-induced modifications. These results suggest that CRF(1) receptor antagonists may represent potential antidepressants.

MeSH terms

  • Animals
  • Depression / drug therapy
  • Disease Models, Animal
  • Drug Therapy, Combination
  • Fluoxetine / administration & dosage
  • Fluoxetine / pharmacology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Pyrimidines / administration & dosage
  • Pyrimidines / pharmacology*
  • Pyrroles / administration & dosage
  • Pyrroles / pharmacology*
  • Receptors, Corticotropin-Releasing Hormone / antagonists & inhibitors*
  • Selective Serotonin Reuptake Inhibitors / administration & dosage
  • Selective Serotonin Reuptake Inhibitors / pharmacology*
  • Stress, Psychological / drug therapy*

Substances

  • Pyrimidines
  • Pyrroles
  • Receptors, Corticotropin-Releasing Hormone
  • Serotonin Uptake Inhibitors
  • antalarmin
  • Fluoxetine