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EDITORIAL article

Front. Behav. Neurosci., 08 November 2013
Sec. Emotion Regulation and Processing
Volume 7 - 2013 | https://doi.org/10.3389/fnbeh.2013.00158

Understanding stress resilience

  • 1Institute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO, USA
  • 2Neurocentre Magendie, INSERM U862, Bordeaux, France
  • 3Department of Psychology and Neuroscience, University of Colorado Boulder, Boulder, CO, USA

Adverse events can impact brain structure and function and are considered primary sources of risk for depression, anxiety, and other psychiatric disorders. However, the majority of individuals who encounter adverse or stressful life events do not develop untoward outcomes, and so an understanding of the factors that promote resistance to the deleterious effects of stress is of clinical importance. At the level of basic research, there has been considerable effort directed at identifying experimental parameters that blunt/augment outcomes from an adverse event, but even when parameters are held constant, there is inter-subject heterogeneity in behavior. This has shifted the focus to understanding how genetic and experiential factors can shape an organism's resistance to future adversity. The articles collected in the present Research Topic provide an overview of recent efforts directed at elucidating the neural mechanisms underlying resilience, and utilizing such information to mitigate vulnerability.

Achieving genetic, epigenetic, and neural circuit-level insight into the causal mechanisms underlying stress resilience has come from a variety of disciplinary approaches. Wu et al. (2013) lead this special issue by providing a comprehensive overview of recent progress in each of these units of analysis. At the human level, much of what is known about the biological determinants of resilience has increasingly come from neuroimaging studies. In this issue van der Werff et al. (2013) examine the structural and functional alterations related to resilience, particularly contrasting findings of individuals who either have, or have not, developed posttraumatic stress disorder (PTSD) following trauma.

One of the consequences of long-term stress exposure is to disrupt processes involved in successful adaptation to environmental threat. The endogenous opioid peptide, β-endorphin, has been shown to facilitate recovery following stress and here Barfield et al. (2013) directly investigate its role in anxiety-like behaviors using transgenic mice with varying capacities to synthesize the peptide. Vander Weele et al. (2013) examine the contribution of another endogenous peptide, growth hormone (GH), in hippocampal dysfunction following prolonged stress. The authors demonstrate that chronic stress regimens reduce hippocampal GH and that stress-induced hippocampal-dependent learning impairments are restored following site-specific viral-mediated overexpression of GH. Their findings implicate GH signaling in the hippocampus as a novel target for promoting resilience following prolonged stress regimens.

Environmental conditions during development also contribute to the heterogeneity of an individual's response to adversity encountered as an adult. As Macrì (2013) outlines, in an opinion piece, developmental conditions may be harnessed to promote resilience in experimental settings. One such experiential factor in humans, access to regular physical activity, has long been known to positively modulate an individual's adaptive capacity in the face of stress, an outcome that is readily observed with voluntary wheel running in rodents (Greenwood and Fleshner, 2011). Here Loughridge et al. (2013) combine laser capture microdissection with microarray expression analysis to investigate novel molecular targets of exercise-induced stress resistance. In addition to several genes that participate in neural mechanisms previously shown to be critical in the impact of exercise on stress, their innovative approach revealed sets of immune- and circadian-related genes that deserve further investigation.

In many organisms, prior exposure to repeated stressors often potentiates the neural and behavioral responses to later adverse events, a phenomenon termed stress sensitization, which is thought to be an important process involved in the susceptibility to anxiety disorders. Conversely, a reduction in autonomic, neuroendocrine, and behavioral responses is observed following repeated exposures to identical stressors (homotypic stress), a phenomenon termed stress habituation. Herman (2013) discusses the mechanisms underlying habituation and the challenges of identifying neural processes that represent a transition from adaptive to maladaptive responding during conditions of chronic challenge.

Psychological and social factors (e.g., coping style, cognitive flexibility, and social support) have long been associated with resilience to adversity (Southwick et al., 2005), although many of these factors are difficult to study in animals where the underlying neural mechanisms can be directly explored. In an animal model of intimate partner violence, Poirier et al. (2013) examine the influence of baseline trait anxiety in female rats on the neural and behavioral consequences of long-term cohabitation with an aggressive male partner. Despite the fact that anxious temperament modulated the behavioral outcome, many of the regional gene expression patterns that are altered by cohabitation did not differ between the “low” and “high” anxiety subgroups, highlighting the growing consensus that mechanisms of resilience are not always the opposite of those mediating vulnerability.

Additional psychosocial factors associated with resilience involve processes that engage coping strategies (Agaibi and Wilson, 2005). Active coping is generally conceptualized as behavioral or psychological efforts that individuals employ to master or reduce negative circumstances. Actual or perceived behavioral control over some aspect of the adverse event is central to coping, and Drugan et al. (2013) provide a review of rodent paradigms in which the degree of behavioral control is experimentally manipulated. The authors further discuss the development of continuous non-invasive measurements (e.g., ultrasonic vocalizations) within the original stress episode that may be predictive of later performance during a subsequent challenge. On a related note, Nechvatal and Lyons (2013) review how coping, within the context of stress exposure therapy, impacts functional and structural measures in patients with specific phobias or PTSD. A long-term goal of this line of research, the authors note, is to guide the development of new intervention modalities that enhance the neuroadaptations associated with coping with stress in order to facilitate recovery.

Overall, the perspectives presented in this Frontiers in Behavioral Neuroscience Research Topic represent an integrative approach for elucidating the neural mechanisms underlying stress resilience. Extension of these efforts to other experimental paradigms may identify common themes that will very likely inform and enhance current therapeutic modalities.

References

Agaibi, C. E., and Wilson, J. P. (2005). Trauma, PTSD, and resilience: a review of the literature. Trauma Violence Abuse 6, 195–216. doi: 10.1177/1524838005277438

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Barfield, E. T., Moser, V. A., Hand, A., and Grisel, J. E. (2013). β-endorphin modulates the effect of stress on novelty-suppressed feeding. Front. Behav. Neurosci. 7:19. doi: 10.3389/fnbeh.2013.00019

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Drugan, R. C., Christianson, J. P., Warner, T. A., and Kent, S. (2013). Resilience in shock and swim stress models of depression. Front. Behav. Neurosci. 7:14. doi: 10.3389/fnbeh.2013.00014

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Greenwood, B. N., and Fleshner, M. (2011). Exercise, stress resistance, and central serotonergic systems. Exerc. Sport Sci. Rev. 39, 140–149. doi: 10.1097/JES.0b013e31821f7e45

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Herman, J. P. (2013). Neural control of chronic stress adaptation. Front. Behav. Neurosci. 7:61. doi: 10.3389/fnbeh.2013.00061

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Loughridge, A. B., Greenwood, B. N., Day, H. E., McQueen, M. B., and Fleshner, M. (2013). Microarray analyses reveal novel targets of exercise-induced stress resistance in the dorsal raphe nucleus. Front. Behav. Neurosci. 7:37. doi: 10.3389/fnbeh.2013.00037

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Macrì, S. (2013). On the incongruity between developmental plasticity and methodological rigidity. Front. Behav. Neurosci. 6:93. doi: 10.3389/fnbeh.2012.00093

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Nechvatal, J. M., and Lyons, D. M. (2013). Coping changes the brain. Front. Behav. Neurosci. 7:13. doi: 10.3389/fnbeh.2013.00013

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Poirier, G. L., Cordero, M. I., and Sandi, C. (2013). Female vulnerability to the development of depression-like behavior in a rat model of intimate partner violence is related to anxious temperament, coping responses, and amygdala vasopressin receptor 1a expression. Front. Behav. Neurosci. 7:35. doi: 10.3389/fnbeh.2013.00035

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Southwick, S. M., Vythilingam, M., and Charney, D. S. (2005). The psychobiology of depression and resilience to stress: implications for prevention and treatment. Annu. Rev. Clin. Psychol. 1:255–291 doi: 10.1146/annurev.clinpsy.1.102803.143948

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Vander Weele, C. M., Saenz, C., Yao, J., Correia, S. S., and Goosens, K. A. (2013). Restoration of hippocampal growth hormone reverses stress-induced hippocampal impairment. Front. Behav. Neurosci. 7:66. doi: 10.3389/fnbeh.2013.00066

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van der Werff, S. J., van den Berg, S. M., Pannekoek, J. N., Elzinga, B. M., and van der Wee, N. J. (2013). Neuroimaging resilience to stress: a review. Front. Behav. Neurosci. 7:39. doi: 10.3389/fnbeh.2013.00039

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Wu, G., Feder, A., Cohen, H., Kim, J. J., Calderon, S., Charney, D. S., et al. (2013). Understanding resilience. Front. Behav. Neurosci. 7:10. doi: 10.3389/fnbeh.2013.00010

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Keywords: resilience, stress, trauma, coping, depression, anxiety, posttraumatic stress disorder, neuroimaging

Citation: Baratta MV, Rozeske RR and Maier SF (2013) Understanding stress resilience. Front. Behav. Neurosci. 7:158. doi: 10.3389/fnbeh.2013.00158

Received: 16 October 2013; Accepted: 22 October 2013;
Published online: 08 November 2013.

Edited by:

Carmen Sandi, Ecole Polytechnique Federale de Lausanne, Switzerland

Copyright © 2013 Baratta, Rozeske and Maier. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: michael.baratta@colorado.edu

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