Evidence map›Paper›PMID 33769022›Full record

ArticleJournal of psychiatry & neuroscience : JPN2021

Sex differences in innate and adaptive neural oscillatory patterns link resilience and susceptibility to chronic stress in rats.

Rachel-Karson Thériault, Joshua D Manduca, Melissa L Perreault

Open access · diamondAbstract read
In one paragraph

Article in Journal of psychiatry & neuroscience : JPN, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Consideration of Research Approaches in Systems Neurobiology.Biological psychiatry global open science · 2024
    Article
  5. Article
  6. Article
  7. Monitoring of Alarm Reactions of Red Deer (Animals : an open access journal from MDPI · 2023
    Article
  8. Selective effects of acute and chronic stress on slow and alpha-theta cortical functional connectivity and reversal with subanesthetic ketamine.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  9. Review
  10. Article
  11. Review
  12. Review
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  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Rachel-Karson ThériaultFrom the department of Molecular and Cellular Biology, University of Guelph, Guelph, Ont., Canada (Thériault, Manduca, Perreault) and the Collaborative Neuroscience Program, University of Guelph, Guelph, Ont., Canada (Thériault, Perreault).
Joshua D ManducaFrom the department of Molecular and Cellular Biology, University of Guelph, Guelph, Ont., Canada (Thériault, Manduca, Perreault) and the Collaborative Neuroscience Program, University of Guelph, Guelph, Ont., Canada (Thériault, Perreault).
Melissa L PerreaultFrom the department of Molecular and Cellular Biology, University of Guelph, Guelph, Ont., Canada (Thériault, Manduca, Perreault) and the Collaborative Neuroscience Program, University of Guelph, Guelph, Ont., Canada (Thériault, Perreault).
University of Guelph · CA

Funding

CIHR
6 · The paper itself

Abstract

Background: Major depressive disorder is a chronic illness with a higher incidence in women. Dysregulated neural oscillatory activity is an emerging mechanism thought to underlie major depressive disorder, but whether sex differences in these rhythms contribute to the development of symptoms is unknown. Methods: We exposed male and female rats to chronic unpredictable stress and characterized them as stress-resilient or stress-susceptible based on behavioural output in the forced swim test and the sucrose preference test. To identify sex-specific neural oscillatory patterns associated with stress response, we recorded local field potentials from the prefrontal cortex, cingulate cortex, nucleus accumbens and dorsal hippocampus throughout stress exposure. Results: At baseline, female stress-resilient rats innately exhibited higher theta coherence in hippocampal connections compared with stress-susceptible female rats. Following stress exposure, additional oscillatory changes manifested: stress-resilient females were characterized by increased dorsal hippocampal theta power and cortical gamma power, and stress-resilient males were characterized by a widespread increase in high gamma coherence. In stress-susceptible animals, we observed a pattern of increased delta and reduced theta power; the changes were restricted to the cingulate cortex and dorsal hippocampus in males but occurred globally in females. Finally, stress exposure was accompanied by the time-dependent recruitment of specific neural pathways, which culminated in system-wide changes that temporally coincided with the onset of depression-like behaviour. Limitations: We could not establish causality between the electrophysiological changes and behaviours with the methodology we employed. Conclusion: Sex-specific neurophysiological patterns can function as early markers for stress vulnerability and the onset of depression-like behaviours in rats.

Indexed as

NeuronsResilience, PsychologicalSex CharacteristicsAnimalsBrainFemaleHippocampusMajor Depressive DisorderMaleRatsStress, Psychological

Identifiers

PMID33769022
PMCPMC8061734
OpenAlexW3139127775

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.