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Publication : Prefrontal cortical circuit for depression- and anxiety-related behaviors mediated by cholecystokinin: role of ΔFosB.

First Author  Vialou V Year  2014
Journal  J Neurosci Volume  34
Issue  11 Pages  3878-87
PubMed ID  24623766 Mgi Jnum  J:209604
Mgi Id  MGI:5568173 Doi  10.1523/JNEUROSCI.1787-13.2014
Citation  Vialou V, et al. (2014) Prefrontal cortical circuit for depression- and anxiety-related behaviors mediated by cholecystokinin: role of DeltaFosB. J Neurosci 34(11):3878-87
abstractText  Decreased medial prefrontal cortex (mPFC) neuronal activity is associated with social defeat-induced depression- and anxiety-like behaviors in mice. However, the molecular mechanisms underlying the decreased mPFC activity and its prodepressant role remain unknown. We show here that induction of the transcription factor DeltaFosB in mPFC, specifically in the prelimbic (PrL) area, mediates susceptibility to stress. DeltaFosB induction in PrL occurred selectively in susceptible mice after chronic social defeat stress, and overexpression of DeltaFosB in this region, but not in the nearby infralimbic (IL) area, enhanced stress susceptibility. DeltaFosB produced these effects partly through induction of the cholecystokinin (CCK)-B receptor: CCKB blockade in mPFC induces a resilient phenotype, whereas CCK administration into mPFC mimics the anxiogenic- and depressant-like effects of social stress. We previously found that optogenetic stimulation of mPFC neurons in susceptible mice reverses several behavioral abnormalities seen after chronic social defeat stress. Therefore, we hypothesized that optogenetic stimulation of cortical projections would rescue the pathological effects of CCK in mPFC. After CCK infusion in mPFC, we optogenetically stimulated mPFC projections to basolateral amygdala or nucleus accumbens, two subcortical structures involved in mood regulation. Stimulation of corticoamygdala projections blocked the anxiogenic effect of CCK, although no effect was observed on other symptoms of social defeat. Conversely, stimulation of corticoaccumbens projections reversed CCK-induced social avoidance and sucrose preference deficits but not anxiogenic-like effects. Together, these results indicate that social stress-induced behavioral deficits are mediated partly by molecular adaptations in mPFC involving DeltaFosB and CCK through cortical projections to distinct subcortical targets.
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