Antidepressant-like effect of aripiprazole via 5-HT1A, D1, and D2 receptors in the prefrontal cortex of olfactory bulbectomized mice

J Pharmacol Sci. 2018 Jul;137(3):241-247. doi: 10.1016/j.jphs.2018.06.006. Epub 2018 Jul 7.

Abstract

Olfactory bulbectomized (OBX) mice exhibit depressive-like behaviors and memory deficits. We have reported that aripiprazole (ARI) ameliorates the behavioral hyper-responsivity to dopamine agonists and memory deficits in OBX mice; however, it is unclear whether ARI affects OBX-induced depressive-like behavior. To address this question, we evaluated the effect of ARI on depressive-like behavior in OBX mice using the forced swim test (FST). In addition, we investigated the effect of ARI on c-Fos expression in the prefrontal cortex (PFC), striatum, and hippocampus of OBX mice using western blotting. OBX mice exhibited a longer immobility duration in the FST 14 days after surgery. Depressive-like behavior in OBX mice was reversed 30 min after administration of ARI (0.01 or 0.03 mg/kg). In addition, c-Fos expression was increased in the PFC, but not the striatum or hippocampus, 30 min after acute administration of ARI. These effects were inhibited by administration of the selective 5-HT1A, D1, and D2 receptor antagonists, WAY100635, SCH23390, and L-741,626, respectively. These findings suggest that ARI produces an antidepressant effect in OBX mice that may be mediated by 5-HT1A, D1, and D2 receptors in the PFC.

Keywords: 5-HT(1A) receptor; Antidepressant; Aripiprazole; Dopamine receptors; Olfactory bulbectomy.

MeSH terms

  • Animals
  • Antidepressive Agents*
  • Antipsychotic Agents / pharmacology*
  • Aripiprazole / pharmacology*
  • Cyclic AMP-Dependent Protein Kinases / genetics
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Gene Expression / drug effects
  • Male
  • Mice, Inbred Strains
  • Olfactory Bulb / physiology*
  • Olfactory Bulb / surgery*
  • Prefrontal Cortex / metabolism*
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / metabolism
  • Receptor, Serotonin, 5-HT1A / metabolism*
  • Receptors, Dopamine D1 / metabolism*
  • Receptors, Dopamine D2 / metabolism*

Substances

  • Antidepressive Agents
  • Antipsychotic Agents
  • Proto-Oncogene Proteins c-fos
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Receptor, Serotonin, 5-HT1A
  • Aripiprazole
  • Cyclic AMP-Dependent Protein Kinases