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

Overview
Journal J Neurosci
Specialty Neurology
Date 2014 May 30
PMID 24872553
Citations 52
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Abstract

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.

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References
1.
Kinou M, Takizawa R, Marumo K, Kawasaki S, Kawakubo Y, Fukuda M . Differential spatiotemporal characteristics of the prefrontal hemodynamic response and their association with functional impairment in schizophrenia and major depression. Schizophr Res. 2013; 150(2-3):459-67. DOI: 10.1016/j.schres.2013.08.026. View

2.
Moscarello J, LeDoux J . Active avoidance learning requires prefrontal suppression of amygdala-mediated defensive reactions. J Neurosci. 2013; 33(9):3815-23. PMC: 3607300. DOI: 10.1523/JNEUROSCI.2596-12.2013. View

3.
Milad M, Quirk G . Fear extinction as a model for translational neuroscience: ten years of progress. Annu Rev Psychol. 2011; 63:129-51. PMC: 4942586. DOI: 10.1146/annurev.psych.121208.131631. View

4.
Vollmayr B, Henn F . Learned helplessness in the rat: improvements in validity and reliability. Brain Res Brain Res Protoc. 2001; 8(1):1-7. DOI: 10.1016/s1385-299x(01)00067-8. View

5.
Mayberg H, Liotti M, Brannan S, McGinnis S, Mahurin R, Jerabek P . Reciprocal limbic-cortical function and negative mood: converging PET findings in depression and normal sadness. Am J Psychiatry. 1999; 156(5):675-82. DOI: 10.1176/ajp.156.5.675. View