Evidence map›Paper›PMID 32471349›Full record

ArticleBMC neuroscience2020

Repeated social defeat promotes persistent inflammatory changes in splenic myeloid cells; decreased expression of β-arrestin-2 (ARRB2) and increased expression of interleukin-6 (IL-6).

Dhaksshaginy Rajalingam, Ingeborg Nymoen, Daniel Pitz Jacobsen, Mina Baarnes Eriksen, Erik Dissen, Morten Birkeland Nielsen, Ståle Valvatne Einarsen, Johannes Gjerstad

Open access · goldAbstract read
In one paragraph

Article in BMC neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 43% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 3 institutions in 1 country.

Dhaksshaginy RajalingamDepartment of Psychosocial Science, University of Bergen, Bergen, Norway. Dhaksshaginy.Rajalingam@uib.no.ORCID 0000-0002-4647-5437
Ingeborg NymoenNational Institute of Occupational Health, Oslo, Norway.
Daniel Pitz JacobsenNational Institute of Occupational Health, Oslo, Norway.
Mina Baarnes EriksenNational Institute of Occupational Health, Oslo, Norway.
Erik DissenInstitute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Morten Birkeland NielsenDepartment of Psychosocial Science, University of Bergen, Bergen, Norway.
Ståle Valvatne EinarsenDepartment of Psychosocial Science, University of Bergen, Bergen, Norway.
Johannes GjerstadDepartment of Psychosocial Science, University of Bergen, Bergen, Norway.
National Institute of Occupational Health · NOUniversity of Bergen · NOUniversity of Oslo · NO

Funding

Forskningsrådet 237777Universitetet i Bergen 250127
6 · The paper itself

Abstract

backgroundPrevious studies suggest that persistent exposure to social stress in mammals may be associated with multiple physiological effects. Here, we examine the effects of social stress in rats, i.e. repeated social defeat, on behavior, hypothalamic-pituitary-adrenal (HPA)-axis and immune system.

methodsA resident-intruder paradigm, where an intruder rat was exposed to social stress by a dominant resident rat for 1 hour each day for 7 consecutive days was used. The day after the last stress exposure in the paradigm the data were analyzed. Variation in social interaction was observed manually, whereas locomotion was analyzed off-line by a purpose-made software. Gene expression in the pituitary gland, adrenal gland and myeloid cells isolated from the spleen was measured by qPCR.

resultsThe exposure to social stress induced decreased weight gain and increased locomotion. An increased nuclear receptor subfamily group C number 1 (NR3C1) expression in the pituitary gland was also shown. In myeloid cells harvested from the spleen, we observed decreased expression of the β

conclusionOur results show that that the experience of social stress in the form of repeated social defeat in rats is a potent stressor that in myeloid cells in the spleen promotes persistent inflammatory changes. Future research is needed to examine whether similar inflammatory changes also can explain the impact of social stress, such as bullying and harassment, among humans.

Indexed as

Social DefeatAnimalsBehavior, Animalbeta-Arrestin 2Hypothalamo-Hypophyseal SystemInflammationInterleukin-6Motor ActivityMyeloid CellsPituitary-Adrenal SystemRats, Long-EvansRats, Sprague-DawleySpleenStress, PsychologicalArrb2 protein, ratbeta-Arrestin 2Il6 protein, ratInterleukin-6ADRB2ARRB2BullyingIL-6Repeated social defeatSocial stressors

Identifiers

PMID32471349
PMCPMC7260804
OpenAlexW3031659968

What Socratic holds

Textmetadata
LicenceCC BY
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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.