Literature DB >> 28606772

Dominance status alters restraint-induced neural activity in brain regions controlling stress vulnerability.

Matthew A Cooper1, Sahba Seddighi2, Abigail K Barnes2, J Alex Grizzell2, Brooke N Dulka2, Catherine T Clinard2.   

Abstract

Understanding the cellular mechanisms that control resistance and vulnerability to stress is an important step toward identifying novel targets for the prevention and treatment of stress-related mental illness. In Syrian hamsters, dominant and subordinate animals exhibit different behavioral and physiological responses to social defeat stress, with dominants showing stress resistance and subordinates showing stress vulnerability. We previously found that dominant and subordinate hamsters show different levels of defeat-induced neural activity in brain regions that modulate coping with stress, although the extent to which status-dependent differences in stress vulnerability generalize to non-social stressors is unknown. In this study, dominant, subordinate, and control male Syrian hamsters were exposed to acute physical restraint for 30min and restraint-induced c-Fos immunoreactivity was quantified in select brain regions. Subordinate animals showed less restraint-induced c-Fos immunoreactivity in the infralimbic (IL), prelimbic (PL), and ventral medial amygdala (vMeA) compared to dominants, which is consistent with the status-dependent effects of social defeat stress. Subordinate animals did not show increased c-Fos immunoreactivity in the rostroventral dorsal raphe nucleus (rvDRN), which is in contrast to the effects of social defeat stress. These findings indicate that status-dependent changes in neural activity generalize from one stressor to another in a brain region-dependent manner. These findings further suggest that while some neural circuits may support a generalized form of stress resistance, others may provide resistance to specific stressors.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anxiety; Coping; Dorsal raphe nucleus; Medial amygdala; Resilience; Social dominance

Mesh:

Substances:

Year:  2017        PMID: 28606772      PMCID: PMC5581240          DOI: 10.1016/j.physbeh.2017.06.003

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  68 in total

1.  Differential expression of c-fos mRNA within neurocircuits of male hamsters exposed to acute or chronic defeat.

Authors:  S Kollack-Walker; C Don; S J Watson; H Akil
Journal:  J Neuroendocrinol       Date:  1999-07       Impact factor: 3.627

2.  Paradoxical enhancement of fear expression and extinction deficits in mice resilient to social defeat.

Authors:  Jeremy D Meduri; Laure A Farnbauch; Aaron M Jasnow
Journal:  Behav Brain Res       Date:  2013-09-09       Impact factor: 3.332

3.  Chronic stress-induced alterations of dendritic spine subtypes predict functional decrements in an hypothalamo-pituitary-adrenal-inhibitory prefrontal circuit.

Authors:  Jason J Radley; Rachel M Anderson; Bradley A Hamilton; Jennifer A Alcock; Sara A Romig-Martin
Journal:  J Neurosci       Date:  2013-09-04       Impact factor: 6.167

Review 4.  Steroid-dependent plasticity in the medial amygdala.

Authors:  B M Cooke
Journal:  Neuroscience       Date:  2005-12-05       Impact factor: 3.590

5.  Differential brain-derived neurotrophic factor expression in limbic brain regions following social defeat or territorial aggression.

Authors:  Stacie L Taylor; Lisa M Stanek; Kerry J Ressler; Kim L Huhman
Journal:  Behav Neurosci       Date:  2011-12       Impact factor: 1.912

6.  Neurons in medial prefrontal cortex signal memory for fear extinction.

Authors:  Mohammed R Milad; Gregory J Quirk
Journal:  Nature       Date:  2002-11-07       Impact factor: 49.962

7.  Blocking corticotropin-releasing factor-2 receptors, but not corticotropin-releasing factor-1 receptors or glucocorticoid feedback, disrupts the development of conditioned defeat.

Authors:  Matthew A Cooper; Kim L Huhman
Journal:  Physiol Behav       Date:  2010-08-10

8.  NR2B subunit of the NMDA receptor in the basolateral amygdala is necessary for the acquisition of conditioned defeat in Syrian hamsters.

Authors:  Diane E Day; Matthew A Cooper; Chris M Markham; Kim L Huhman
Journal:  Behav Brain Res       Date:  2010-10-08       Impact factor: 3.332

9.  Evidence supporting a role for corticotropin-releasing factor type 2 (CRF2) receptors in the regulation of subpopulations of serotonergic neurons.

Authors:  Daniel R Staub; Andrew K Evans; Christopher A Lowry
Journal:  Brain Res       Date:  2006-01-03       Impact factor: 3.252

10.  Neurobiological correlates of high (HAB) versus low anxiety-related behavior (LAB): differential Fos expression in HAB and LAB rats.

Authors:  Nicolas Salomé; Peter Salchner; Odile Viltart; Henrique Sequeira; Alexandra Wigger; Rainer Landgraf; Nicolas Singewald
Journal:  Biol Psychiatry       Date:  2004-04-01       Impact factor: 13.382

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  3 in total

1.  Gonadal steroid hormone receptors in the medial amygdala contribute to experience-dependent changes in stress vulnerability.

Authors:  Matthew A Cooper; Catherine T Clinard; Brooke N Dulka; J Alex Grizzell; Annie L Loewen; Ashley V Campbell; Samuel G Adler
Journal:  Psychoneuroendocrinology       Date:  2021-05-03       Impact factor: 4.693

Review 2.  Using social rank as the lens to focus on the neural circuitry driving stress coping styles.

Authors:  Katherine B LeClair; Scott J Russo
Journal:  Curr Opin Neurobiol       Date:  2021-04-27       Impact factor: 7.070

3.  Activity of a vmPFC-DRN Pathway Corresponds With Resistance to Acute Social Defeat Stress.

Authors:  J Alex Grizzell; Thomas T Clarity; Nate B Graham; Brooke N Dulka; Matthew A Cooper
Journal:  Front Neural Circuits       Date:  2020-10-16       Impact factor: 3.492

  3 in total

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