Abstract

Stress increases vulnerability to psychiatric disorders, partly by affecting brain monoamine systems, such as the locus coeruleus (LC)-norepinephrine system. During stress, LC activity is coregulated by corticotropin-releasing factor (CRF) and endogenous opioids. This study identified neural circuitry that regulates LC activity of intruder rats during the resident-intruder model of social stress. LC afferents were retrogradely labeled with Fluorogold (FG) and rats were subjected to one or five daily exposures to an aggressive resident. Sections through the nucleus paragigantocellularis (PGi) and central amygdalar nucleus (CNA), major sources of enkephalin (ENK) and CRF LC afferents, respectively, were immunocytochemically processed to detect c-fos, FG, and CRF or ENK. In response to a single exposure, intruder rats assumed defeat with a relatively short latency (SL). LC neurons, PGI-ENK LC afferents, and CNA-CRF LC afferents were activated in these rats as indicated by increased c-fos expression. With repeated stress, rats exhibited either a SL or long latency (LL) to defeat and these strategies were associated with distinct patterns of neuronal activation. In SL rats, LC neurons were activated, as were CNA-CRF LC afferents but not PGI-ENK LC afferents. LL rats had an opposite pattern, maintaining activation of PGi-ENK LC afferents but not CNA-CRF LC afferents or LC neurons. Together, these results indicate that the establishment of different coping strategies to social stress is associated with changes in the circuitry that regulates activity of the brain norepinephrine system. This may underlie differential vulnerability to the consequences of social stress that characterize these different coping strategies.

Highlights

  • Successful adaptation to stressors requires the coordination of multiple stress response systems that mount adaptive endocrine, autonomic, immunologic, and behavioral responses

  • Retrograde tract tracing from the locus coeruleus (LC) was combined with immunohistochemistry to detect c-fos, a marker of neuronal activation, and either corticotropin-releasing factor (CRF) or ENK in LC afferents of rats exposed to repeated resident–intruder stress

  • These sections were washed in 0.1 M Tris buffered saline (TBS), pH 7.6, and eNeuro.sfn.org incubated in 0.5% bovine serum albumin (BSA) in TBS for 30 min

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Summary

Introduction

Successful adaptation to stressors requires the coordination of multiple stress response systems that mount adaptive endocrine, autonomic, immunologic, and behavioral responses. Given the decreased vulnerability of LL rats to rodent endpoints of stress-related psychiatric disorders, identifying neurobiological substrates and circuitry that distinguish the SL and LL phenotypes may reveal the basis for different stress coping strategies as well as vulnerability to stress-related pathology. Retrograde tract tracing from the LC was combined with immunohistochemistry to detect c-fos, a marker of neuronal activation, and either CRF or ENK in LC afferents of rats exposed to repeated resident–intruder stress. To determine how this differed from rats exposed to an acute resident–intruder stress before the divergence of different coping strategies, similar approaches were applied to rats exposed to a single session of resident–intruder stress

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