Chronic unpredictable stress promotes neuronal apoptosis in the cerebral cortex

Neurosci Lett. 2008 Sep 12;442(2):104-8. doi: 10.1016/j.neulet.2008.06.081. Epub 2008 Jul 3.

Abstract

Stress-mediated loss of synaptogenesis in the hippocampus appears to play a role in depressive and mood disorders. However, little is known about the effect of stress/depression on the plasticity and survival of cortical neurons. In this report, we have examined whether chronic stress increases the vulnerability of neurons in the rat cortex. We have used a chronic unpredictable mild stress (CMS) as a rat model of depression. CMS (5 weeks treatment) produced anedonia and increased corticosterone levels. These effects were accompanied by a detectable increase in caspase-3 positive neurons in the cerebral cortex, suggesting apoptosis. Desipramine (DMI), a well known antidepressant, reversed the pro-apoptotic effect of CMS. These results suggest that antidepressants may reduce the pathological changes seen in stress-induced depressive disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antidepressive Agents, Tricyclic / pharmacology
  • Antidepressive Agents, Tricyclic / therapeutic use
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Caspase 3 / metabolism
  • Cerebral Cortex / pathology*
  • Cerebral Cortex / physiopathology
  • Chronic Disease
  • Corticosterone / blood
  • Desipramine / pharmacology
  • Desipramine / therapeutic use
  • Disease Models, Animal
  • Male
  • Neurons / drug effects
  • Neurons / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Stress, Psychological / blood
  • Stress, Psychological / drug therapy
  • Stress, Psychological / pathology*

Substances

  • Antidepressive Agents, Tricyclic
  • Caspase 3
  • Desipramine
  • Corticosterone