Environmental enrichment has antidepressant-like action without improving learning and memory deficits in olfactory bulbectomized rats

Neuropharmacology. 2012 Jan;62(1):270-7. doi: 10.1016/j.neuropharm.2011.07.018. Epub 2011 Jul 22.

Abstract

Depression, especially in the elderly, is associated with poor cognitive functioning. Exercise has received much attention in the treatment for depression and also dementia. Here we studied the effect of an enriched environment combined with voluntary exercise (EE/VE) on the olfactory bulbectomized (OBX) rat. The OBX rat is hyperactive in an open field, which is normalized by chronic antidepressant treatment, and suffers from learning and memory impairments. Neurotrophic factors are thought to be involved in the antidepressant action of EE/VE. Hyperactivity and cognitive functioning (both hippocampal dependent and independent tasks) were investigated before and after EE/VE. We quantified hippocampal mRNA levels of the neurotrophic factors BDNF, VGF and VEGF. VEGF receptor (FLK-1) inhibition was achieved by i.c.v administration of the antagonist SU5416 during the period of EE/VE. OBX almost completely blocked fear memory acquired either 48 h or 28 days before surgery. EE/EV normalized OBX-induced hyperactivity in open field, while having no effect on the decrease in hippocampal dependent learning and memory. VEGF mRNA levels in hippocampus were significantly increased both in OBX and control rats following EE/VE. OBX reduced BDNF mRNA levels, but EE did not reverse this. Inhibition of the FLK-1 receptor did not suppress EE/VE induced normalization of the hyperactivity of the OBX rat. The lack of effect of EE/VE on cognitive parameters, while normalizing hyperactivity, suggests different neuronal mechanisms underlying OBX-induced behavioral changes. Since EE/VE still normalizes the OBX-induced hyperactivity while the FLK-1 receptor was blocked, we assume that VEGF is not obligatory for the antidepressant effect of EE/VE. This article is part of a Special Issue entitled 'Anxiety and Depression'.

MeSH terms

  • Analysis of Variance
  • Animals
  • Avoidance Learning / physiology
  • Body Weight / drug effects
  • Body Weight / physiology
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • Depression / therapy*
  • Disease Models, Animal
  • Environment*
  • Exercise Therapy
  • Exploratory Behavior / drug effects
  • Exploratory Behavior / physiology
  • Indoles / pharmacology
  • Indoles / therapeutic use
  • Learning Disabilities / etiology
  • Learning Disabilities / therapy*
  • Locomotion / drug effects
  • Locomotion / physiology
  • Maze Learning / drug effects
  • Maze Learning / physiology
  • Memory Disorders / etiology
  • Memory Disorders / therapy*
  • Olfactory Bulb / drug effects
  • Olfactory Bulb / injuries
  • Olfactory Bulb / physiopathology*
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrroles / pharmacology
  • Pyrroles / therapeutic use
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Recognition, Psychology / physiology
  • Time Factors
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • Indoles
  • Protein Kinase Inhibitors
  • Pyrroles
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A
  • Semaxinib