Chronic unpredictable stress promotes neuronal apoptosis in the cerebral cortex

被引:114
作者
Bachis, Alessia [1 ]
Cruz, Maria Idalia [1 ]
Nosheny, Rachel L. [1 ]
Mocchetti, Italo [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20057 USA
关键词
caspase-3; chronic mild stress (CMS); depression; desipramine (DMI); cerebral cortex;
D O I
10.1016/j.neulet.2008.06.081
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:104 / 108
页数:5
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