Social stress is arguably the predominant form of stress encountered by mammals, and in humans this type of stress contributes to a variety of diseases and psychopathologies. Most research on stress effects do not use social stressors, however. Instead, many animal models of human stress-related disorders use stressors such as intermittent foot shock that offer the benefit of being highly controllable but that may bear little resemblance to stressors encountered in the lives of humans or non-humans. Animal models using a social context closer to that which individuals might experience in their natural environment (so-called ethological models) are essential to a better understanding of the neural mechanisms underlying social behavior, in general, and experience-dependent behavioral plasticity, in particular. We propose that conditioned defeat in hamsters is a unique, ethologically relevant model of stress-induced behavioral plasticity wherein a single, brief exposure to a social stressor reliably induces profound and long-lasting changes in social behavior. We also emphasize that studying models such as conditioned defeat is critical to an improved understanding of stress-related psychopathologies in humans and to the development of better treatment options for these disorders. We have demonstrated that the basolateral nucleus of the amygdala is critical to the acquisition and expression of conditioned defeat in hamsters, but we also have evidence that other brain areas are involved in the production of this behavioral change.
The specific aims of this project will 1) define the broader neural Circuitry mediating conditioned defeat. This is important because it will allow us to concurrently study multiple brain systems that are usually examined in isolation from one another and will ultimately help us to understand how the brain """"""""selects"""""""" which of a broad repertoire of behaviors is elicited in a particular situation. We will also 2) determine where in the neural circuit the critical plasticity occurs to mediate conditioned defeat and 3) describe some of the cellular/molecular changes that underlie social stress-induced changes in behavior. Social conflict is a major form of stress for humans, and exposure to this type of stress contributes to a variety of diseases and psychopathologies including depression and anxiety disorders. Understanding of the neural events that underlie conditioned defeat, a social stress-induced behavioral change, will improve our understanding of how stress changes the brain and subsequent behavior and should lead to the development of better treatment options for individuals with mood and anxiety disorders. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
2R01MH062044-05A1
Application #
7315063
Study Section
Neuroendocrinology, Neuroimmunology, and Behavior Study Section (NNB)
Program Officer
Simmons, Janine M
Project Start
2000-08-01
Project End
2012-05-31
Budget Start
2007-09-10
Budget End
2008-05-31
Support Year
5
Fiscal Year
2007
Total Cost
$292,613
Indirect Cost
Name
Georgia State University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
837322494
City
Atlanta
State
GA
Country
United States
Zip Code
30302
McCann, Katharine E; Sinkiewicz, David M; Rosenhauer, Anna M et al. (2018) Transcriptomic Analysis Reveals Sex-Dependent Expression Patterns in the Basolateral Amygdala of Dominant and Subordinate Animals After Acute Social Conflict. Mol Neurobiol :
Partrick, Katherine A; Chassaing, Benoit; Beach, Linda Q et al. (2018) Acute and repeated exposure to social stress reduces gut microbiota diversity in Syrian hamsters. Behav Brain Res 345:39-48
Ross, Amy P; Norvelle, Alisa; Choi, Dennis C et al. (2017) Social housing and social isolation: Impact on stress indices and energy balance in male and female Syrian hamsters (Mesocricetus auratus). Physiol Behav 177:264-269
McCann, Katharine E; Rosenhauer, Anna M; Jones, Genna M F et al. (2017) Histone deacetylase and acetyltransferase inhibitors modulate behavioral responses to social stress. Psychoneuroendocrinology 75:100-109
Rosenhauer, Anna M; McCann, Katharine E; Norvelle, Alisa et al. (2017) An acute social defeat stressor in early puberty increases susceptibility to social defeat in adulthood. Horm Behav 93:31-38
McCann, Katharine E; Sinkiewicz, David M; Norvelle, Alisa et al. (2017) De novo assembly, annotation, and characterization of the whole brain transcriptome of male and female Syrian hamsters. Sci Rep 7:40472
Gray, C L; Norvelle, A; Larkin, T et al. (2015) Dopamine in the nucleus accumbens modulates the memory of social defeat in Syrian hamsters (Mesocricetus auratus). Behav Brain Res 286:22-8
Gray, Cloe Luckett; Krebs-Kraft, Desiree L; Solomon, Matia B et al. (2015) Immediate post-defeat infusions of the noradrenergic receptor antagonist propranolol impair the consolidation of conditioned defeat in male Syrian hamsters. Physiol Behav 152:56-61
McCann, Katharine E; Bicknese, Corinne N; Norvelle, Alisa et al. (2014) Effects of inescapable versus escapable social stress in Syrian hamsters: the importance of stressor duration versus escapability. Physiol Behav 129:25-9
Song, Zhimin; McCann, Katharine E; McNeill 4th, John K et al. (2014) Oxytocin induces social communication by activating arginine-vasopressin V1a receptors and not oxytocin receptors. Psychoneuroendocrinology 50:14-9

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