Corticotropin-releasing factor in ventromedial prefrontal cortex mediates avoidance of a traumatic stress-paired context. (February 2017)

• Record Type: Journal Article
• Authors: Schreiber, Allyson L.; Lu, Yi-Ling; Baynes, Brittni B.; Richardson, Heather N.; Gilpin, Nicholas W.
• Is Part Of: Neuropharmacology. Volume 113:Part A(2017)
• Page Start: 323
• Page End: 330
• Publication Date: 2017-02
• Subjects: Post-traumatic stress disorder (PTSD) -- Avoidance -- Alcohol self-administration -- Medial prefrontal cortex (mPFC) -- Corticotropin-releasing factor (CRF) -- Anxiety; Neuropsychopharmacology -- Periodicals; Autonomic Agents -- Periodicals; Neuropsychopharmacologie -- Périodiques; Neuropsychopharmacology; Periodicals; Electronic journals; 615.78
• DOI: 10.1016/j.neuropharm.2016.05.008
• Languages: English
• ISSNs: 0028-3908

Abstract

Abstract: Post-traumatic stress disorder (PTSD) affects 7.7 million Americans. One diagnostic criterion for PTSD is avoidance of stimuli that are related to the traumatic stress. Using a predator odor stress conditioned place aversion (CPA) model, rats can be divided into groups based on stress reactivity, as measured by avoidance of the odor-paired context. Avoider rats, which show high stress reactivity, exhibit persistent avoidance of stress-paired context and escalated alcohol drinking. Here, we examined the potential role of corticotropin-releasing factor (CRF), a neuropeptide that promotes anxiety-like behavior in mediating avoidance and escalated alcohol drinking after stress. CRF is expressed in the medial prefrontal cortex (mPFC). The dorsal and ventral sub-regions of the mPFC (dmPFC and vmPFC) have opposing roles in stress reactivity and alcohol drinking. We hypothesized that vmPFC CRF-CRFR1 signaling contributes functionally to stress-induced avoidance and escalated alcohol self-administration. In Experiment 1, adult male Wistar rats were exposed to predator odor stress in a CPA paradigm, indexed for avoidance of odor-paired context, and brains processed for CRF-immunoreactive cell density in vmPFC and dmPFC. Post-stress, Avoiders exhibited higher CRF cell density in vmPFC, but not the dmPFC. In Experiment 2, rats were tested for avoidance of a context repeatedly paired with intra-vmPFC CRF infusions. In Experiment 3, rats were stressed and indexed, then tested for the effects of intra-vmPFC CRFR1 antagonism on avoidance and alcohol self-administration. Intra-vmPFC CRF infusion produced avoidance of a paired context, and intra-vmPFC CRFR1 antagonism reversed avoidance of a stress-paired context, but did not alter post-stress alcohol self-administration. These findings suggest that vmPFC CRF-CRFR1 signaling mediates avoidance of stimuli paired with traumatic stress. Highlights: Predator odor stress increases CRF peptide content in vmPFC of rats that avoid a stress-paired context. Predator odor stress increases CRF cell counts in vmPFC of rats that avoid a stress-paired context. CRF infusions in the vmPFC produce conditioned avoidance. CRF1 receptor antagonism reduces avoidance of a stress-paired context. CRF1 receptor antagonism does not affect post-stress alcohol drinking.