Synaptic Modifications in the Medial Prefrontal Cortex in Susceptibility and Resilience to Stress

被引:81
|
作者
Wang, Minghui [1 ]
Perova, Zinaida [1 ,2 ]
Arenkiel, Benjamin R. [3 ]
Li, Bo [1 ,2 ]
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] Watson Sch Biol Sci, Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[3] Baylor Coll Med, Houston, TX 77030 USA
来源
JOURNAL OF NEUROSCIENCE | 2014年 / 34卷 / 22期
基金
美国国家卫生研究院;
关键词
c-Fos; chemical-genetic; depression; excitatory synapses; learned helplessness; mPFC; LEARNED HELPLESSNESS MODEL; DORSAL RAPHE NUCLEUS; DEEP BRAIN-STIMULATION; CAPSAICIN RECEPTOR; COGNITIVE CONTROL; NEURAL CIRCUITS; MOOD DISORDERS; MICE LACKING; DEPRESSION; AMYGDALA;
D O I
10.1523/JNEUROSCI.5294-13.2014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
When facing stress, most individuals are resilient whereas others are prone to developing mood disorders. The brain mechanisms underlying such divergent behavioral responses remain unclear. Here we used the learned helplessness procedure in mice to examine the role of the medial prefrontal cortex (mPFC), a brain region highly implicated in both clinical and animal models of depression, in adaptive and maladaptive behavioral responses to stress. We found that uncontrollable and inescapable stress induced behavioral state-dependent changes in the excitatory synapses onto a subset of mPFC neurons: those that were activated during behavioral responses as indicated by their expression of the activity reporter c-Fos. Whereas synaptic potentiation was linked to learned helplessness, a depression-like behavior, synaptic weakening, was associated with resilience to stress. Notably, enhancing the activity of mPFC neurons using a chemical-genetic method was sufficient to convert the resilient behavior into helplessness. Our results provide direct evidence that mPFC dysfunction is linked to maladaptive behavioral responses to stress, and suggest that enhanced excitatory synaptic drive onto mPFC neurons may underlie the previously reported hyperactivity of this brain region in depression.
引用
收藏
页码:7485 / 7492
页数:8
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