Journal article
Prefrontal cortex reactivity underlies trait vulnerability to chronic social defeat stress
Nature communications, Vol.5(1), pp.4537-4537
07/29/2014
DOI: 10.1038/ncomms5537
PMCID: PMC4148151
PMID: 25072279
Abstract
Psychological stress contributes to the onset and exacerbation of nearly all neuropsychiatric disorders. Individual differences in stress-regulatory circuits can therefore dramatically affect vulnerability to these illnesses. Here we identify neural circuit mechanisms underlying individual differences in vulnerability to stress using a murine model of chronic social defeat stress. In chronically stressed mice, we find that the degree of prefrontal cortex (PFC) control of amygdala activity predicts stress susceptibility in individual mice. Critically, we also find that individual differences in PFC activation (that is, reactivity) during exposure to an aggressor mouse predict the emergence stress-induced behavioural deficits in stress-naïve mice. Finally, we show that naturally occurring differences in PFC reactivity directly correspond to the intrinsic firing rate of PFC neurons. This demonstrates that naturally occurring differences in PFC function underlie individual differences in vulnerability to stress, raising the hypothesis that PFC modulation may prevent stress-induced psychiatric disorders.
Details
- Title: Subtitle
- Prefrontal cortex reactivity underlies trait vulnerability to chronic social defeat stress
- Creators
- Sunil Kumar - 1] Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina 27710, USARainbo Hultman - 1] Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina 27710, USADalton Hughes - Meyerhoff Scholarship Program, University of Maryland Baltimore County, Baltimore, Maryland 21250, USANadine Michel - Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina 27710, USABrittany M Katz - Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina 27710, USAKafui Dzirasa - 1] Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina 27710, USA Center for Neuroengineering, Duke University Medical Center, Durham, North Carolina 27710, USA Duke Institute for Brain Sciences, Duke University Medical Center, Durham, North Carolina 27710, USA Department of Biomedical Engineering and Neurobiology, Duke University Medical Center, Durham, North Carolina 27710, USA
- Resource Type
- Journal article
- Publication Details
- Nature communications, Vol.5(1), pp.4537-4537
- Publisher
- England
- DOI
- 10.1038/ncomms5537
- PMID
- 25072279
- PMCID
- PMC4148151
- ISSN
- 2041-1723
- eISSN
- 2041-1723
- Grant note
- R37MH073853 / NIMH NIH HHS R01MH099192 / NIMH NIH HHS R01 MH099192 / NIMH NIH HHS R37 MH073853 / NIMH NIH HHS
- Language
- English
- Date published
- 07/29/2014
- Academic Unit
- Molecular Physiology and Biophysics; Psychiatry; Iowa Neuroscience Institute
- Record Identifier
- 9984065853802771
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