Evidence map›Paper›PMID 33434400›Full record

ArticleBrain and behavior2021

Phenotypic characterization of frontal cortex microglia in a rat model of post-traumatic stress disorder.

Thomas S Cotrone, Charina B Hocog, Joseph T Ramsey, Marcus A Sanchez, Heather M Sullivan, Angus G Scrimgeour

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Thomas S CotroneMilitary Nutrition Division, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.ORCID 0000-0002-4016-7572
Charina B HocogVeterinary Support and Oversight Branch, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
Joseph T RamseyVeterinary Support and Oversight Branch, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
Marcus A SanchezVeterinary Support and Oversight Branch, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
Heather M SullivanVeterinary Support and Oversight Branch, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
Angus G ScrimgeourMilitary Nutrition Division, U.S. Army Research Institute of Environmental Medicine, Natick, MA, USA.
U.S. Army Research Institute of Environmental Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPost-traumatic stress disorder (PTSD) is an anxiety disorder induced by psychologically traumatic events. Using a rat model, this study aimed to determine whether psychological trauma alters relative expression between pro-inflammatory and anti-inflammatory markers in microglia. To meet this goal, expression of genes encoding i-NOS, arginase, TNF-α, interleukin-10, CD74, and Mannose Receptor C was analyzed on multiple days following trauma exposure.

methodsSingle-prolonged stress (SPS) was used to model PTSD in male Sprague-Dawley rats. Twenty-four rats (12 Controls and 12 SPS-exposed) were sacrificed on Days 1, 3, and 7 post-SPS. Twenty-four (12 Controls and 12 SPS-exposed) additional rats were exposed to classical fear conditioning on Day 7, and fear extinction on Days 8, 9, 10, 15, 16, and 17. Freezing behavior was measured to assess fear resolution. Microglial isolates were collected from the frontal cortex, and RNA was extracted. Changes in relative expression of target genes were quantified via RT-PCR.

resultsSPS rats showed significant decreases in IL-10 and TNF-α expression and increases in the i-NOS:Arginase and TNF-α:IL-10 ratios compared to Controls on Day 1, but not on Day 3 or Day 7 for any of the dependent variables. Day 17 SPS rats showed a significant decrease in IL-10 expression and an increase in the TNF-α:IL-10 ratio, further characterized by a significant inverse relationship between IL-10 expression and fear persistence.

conclusionPsychological trauma impacts the immunological phenotype of microglia of the frontal cortex. Consequently, future studies should further evaluate the mechanistic role of microglia in PTSD pathology.

Indexed as

Stress Disorders, Post-TraumaticAnimalsDisease Models, AnimalExtinction, PsychologicalFearFrontal LobeMaleMicrogliaPhenotypeRatsRats, Sprague-DawleyStress, PsychologicalFear ExtinctionMicrogliaPost-traumatic Stress DisorderPTSDRatSingle Prolonged StressSPS

Identifiers

PMID33434400
PMCPMC7994680
OpenAlexW3119915319

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LicenceCC BY
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Registered trials

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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.