Abstract

Tremendous individual differences exist in stress responsivity and social defeat stress is a key approach for identifying cellular mechanisms of stress susceptibility and resilience. Syrian hamsters show reliable territorial aggression, but after social defeat they exhibit a conditioned defeat (CD) response characterized by increased submission and an absence of aggression in future social interactions. Hamsters that achieve social dominance prior to social defeat exhibit greater defeat-induced neural activity in infralimbic (IL) cortex neurons that project to the basolateral amygdala (BLA) and reduced CD response compared to subordinate hamsters. Here, we hypothesize that chemogenetic activation of an IL-to-BLA neural projection during acute social defeat will reduce the CD response in subordinate hamsters and thereby produce dominant-like behavior. We confirmed that clozapine-N-oxide (CNO) itself did not alter the CD response and validated a dual-virus, Cre-dependent, chemogenetic approach by showing that CNO treatment increased c-Fos expression in the IL and decreased it in the BLA. We found that CNO treatment during social defeat reduced the acquisition of CD in subordinate, but not dominant, hamsters. This project extends our understanding of the neural circuits underlying resistance to acute social stress, which is an important step toward delineating circuit-based approaches for the treatment of stress-related psychopathologies.

Highlights

  • Tremendous individual differences exist in stress responsivity and social defeat stress is a key approach for identifying cellular mechanisms of stress susceptibility and resilience

  • We have previously shown that after achieving social dominance, male Syrian hamsters display less submissive and defensive behavior during conditioned defeat (CD) testing when compared to subordinates and animals without a dominance rank, which indicates that social dominance promotes resistance to the CD response[22]

  • We used a Designer Receptor Exclusively Activated by Designer Drugs (DREADD) strategy to test the hypothesis that chemogenetic activation of an IL-to-basolateral amygdala (BLA) pathway during acute social defeat stress would be sufficient to promote a dominant-like CD response in subordinate hamsters

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Summary

Introduction

Tremendous individual differences exist in stress responsivity and social defeat stress is a key approach for identifying cellular mechanisms of stress susceptibility and resilience. Hamsters that achieve social dominance prior to social defeat exhibit greater defeat-induced neural activity in infralimbic (IL) cortex neurons that project to the basolateral amygdala (BLA) and reduced CD response compared to subordinate hamsters. We hypothesize that chemogenetic activation of an IL-to-BLA neural projection during acute social defeat will reduce the CD response in subordinate hamsters and thereby produce dominant-like behavior. Chemogenetic activation of IL neurons that send projections www.nature.com/scientificreports to the basolateral amygdala (BLA) facilitates the extinction of conditioned fear in mice[18] These findings from humans and rodents suggest that a direct neural projection between vmPFC and amygdala contributes to emotion regulation, fear extinction, and stress resilience. We demonstrated that dominant hamsters preferentially activate BLA-projecting IL neurons during acute social defeat stress, while subordinates and social status controls do not[25]. We predicted that chemogenetic activation of an IL-to-BLA pathway during social defeat would reduce the CD response in subordinate, but not dominant, hamsters

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