Evidence map›Paper›PMID 35866213›Full record

ArticleJournal of neuroendocrinology2022

The emotional impact of disrupted environmental contexts: Enrichment loss and coping profiles influence stress response recovery in Long-Evans rats.

Molly Kent, Dmitry Kovalev, Benjamin Hart, Danielle Leserve, Gabriella Handford, Dylan Vavra, Kelly Lambert

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroendocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Potential resilience treatments for orangutans (Animal welfare (South Mimms, England) · 2023
    Article
  3. 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

7 authors at 2 institutions in 1 country.

Molly KentDepartment of Biology, Virginia Military Institute, Lexington, VA, USA.
Dmitry KovalevDepartment of Psychology, University of Richmond, Richmond, VA, USA.
Benjamin HartDepartment of Psychology, University of Richmond, Richmond, VA, USA.
Danielle LeserveDepartment of Psychology, University of Richmond, Richmond, VA, USA.
Gabriella HandfordDepartment of Biology, Virginia Military Institute, Lexington, VA, USA.
Dylan VavraDepartment of Psychology, University of Richmond, Richmond, VA, USA.
Kelly LambertDepartment of Psychology, University of Richmond, Richmond, VA, USA.ORCID 0000-0003-1626-5129
University of Richmond · USVirginia Military Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With increasing rates of anxiety and mood disorders across the world, there is an unprecedented need for preclinical animal models to generate translational results for humans experiencing disruptive emotional symptoms. Considering that life events resulting in a perception of loss are correlated with depressive symptoms, the enrichment-loss rodent model offers promise as a translational model for stress-initiated psychiatric disorders. Additionally, predisposed temperament characteristics such as coping styles have been found to influence an individual's stress response. Accordingly, male rats were profiled as either consistent or flexible copers and assigned to one of three environments: standard laboratory housing, enriched environment, or enriched environment exposure followed by downsizing to standard laboratory cages (i.e., enrichment-loss group). Throughout the study, several behaviors were assessed to determine stress, social, and reward-processing responses. To assess recovery of the stress response, fecal samples were collected following the swim stress in 3-h increments to determine the recovery trajectory of corticosterone (CORT) and dehydroepiandrosterone (DHEA) metabolite levels. Upon death, neural markers of neuroplasticity including doublecortin, glial fibrillary acidic factor, and brain-derived neurotrophic factor were assessed via immunohistochemistry. Results indicated the flexible coping animals in the continuous enriched group had higher DHEA/CORT ratios (consistent with adaptive responses in past research); furthermore, the enrichment-loss animals exhibited a blunted CORT response throughout the assessments and enriched flexible copers had faster CORT recovery rates than consistent copers. Standard housed animals exhibited less exploratory behavior in the open field task and continuous enriched, flexible rats consumed more food rewards than the other groups. No differences in neuroplasticity neural markers were observed. In sum, the results of the present study support past research indicating the disruptive consequences of enrichment-loss, providing evidence that the model represents a valuable approach for the investigation of neurobiological mechanisms contributing to interindividual variability in responses to changing experiential landscapes.

Indexed as

Housing, AnimalStress, PsychologicalAdaptation, PsychologicalAnimalsCorticosteroneDehydroepiandrosteroneHumansMaleRatsRats, Long-EvansCorticosteroneDehydroepiandrosteronecopingcorticosteronedehydroepiandrosterone (DHEA)enrichment lossstress

Identifiers

PMID35866213
PMCPMC9540572
OpenAlexW4283368431

What OpenQuestion 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 OpenQuestion graph.