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Neurobiol Stress. 2017 May 6;7:137-151. doi: 10.1016/j.ynstr.2017.05.001. eCollection 2017 Dec.

Circuit and synaptic mechanisms of repeated stress: Perspectives from differing contexts, duration, and development.

Author information

1
Department of Cognitive Linguistic and Psychological Sciences, Brown University, Providence, RI 02912, United States.
2
Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States.
3
Department of Pharmacology, Weill Cornell Medical College, New York, NY 10065, United States.
4
Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, OH 45237, United States.
5
Department of Psychiatry, Yale School of Medicine, New Haven, CT 06508, United States.
6
Department of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, United States.

Abstract

The current review is meant to synthesize research presented as part of a symposium at the 2016 Neurobiology of Stress workshop in Irvine California. The focus of the symposium was "Stress and the Synapse: New Concepts and Methods" and featured the work of several junior investigators. The presentations focused on the impact of various forms of stress (altered maternal care, binge alcohol drinking, chronic social defeat, and chronic unpredictable stress) on synaptic function, neurodevelopment, and behavioral outcomes. One of the goals of the symposium was to highlight the mechanisms accounting for how the nervous system responds to stress and their impact on outcome measures with converging effects on the development of pathological behavior. Dr. Kevin Bath's presentation focused on the impact of disruptions in early maternal care and its impact on the timing of hippocampus maturation in mice, finding that this form of stress drove accelerated synaptic and behavioral maturation, and contributed to the later emergence of risk for cognitive and emotional disturbance. Dr. Scott Russo highlighted the impact of chronic social defeat stress in adolescent mice on the development and plasticity of reward circuity, with a focus on glutamatergic development in the nucleus accumbens and mesolimbic dopamine system, and the implications of these changes for disruptions in social and hedonic response, key processes disturbed in depressive pathology. Dr. Kristen Pleil described synaptic changes in the bed nuclei of the stria terminalis that underlie the behavioral consequences of allostatic load produced by repeated cycles of alcohol binge drinking and withdrawal. Dr. Eric Wohleb and Dr. Ron Duman provided new data associating decreased mammalian target of rapamycin (mTOR) signaling and neurobiological changes in the synapses in response to chronic unpredictable stress, and highlighted the potential for the novel antidepressant ketamine to rescue synaptic and behavioral effects. In aggregate, these presentations showcased how divergent perspectives provide new insights into the ways in which stress impacts circuit development and function, with implications for understanding emergence of affective pathology.

KEYWORDS:

Bed nuclei of the stria terminalis; Corticotropin-releasing factor; Early-life stress; Hippocampus; Major depressive disorder; Mammalian target of rapamycin; Neuropeptide Y; Nucleus accumbens; Prefrtonal cortex; Resilience; Susceptibility

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