Evidence map›Paper›PMID 35281473›Full record

ArticleOxidative medicine and cellular longevity2022

Temporal Characterization of Microglia-Associated Pro- and Anti-Inflammatory Genes in a Neonatal Inflammation-Sensitized Hypoxic-Ischemic Brain Injury Model.

Maria E Bernis, Yvonne Schleehuber, Margit Zweyer, Elke Maes, Ursula Felderhoff-Müser, Daniel Picard, Hemmen Sabir

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 26 citations in OpenAlex.

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  11. NLRP3 inflammasome: a key player in neonatal brain injury.Clinical and experimental pediatrics · 2025
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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

7 authors at 3 institutions in 1 country.

Maria E BernisDepartment of Neonatology and Pediatric Intensive Care, Children's Hospital University of Bonn, Bonn, Germany.
Yvonne SchleehuberDepartment of Neonatology and Pediatric Intensive Care, Children's Hospital University of Bonn, Bonn, Germany.
Margit ZweyerDepartment of Neonatology and Pediatric Intensive Care, Children's Hospital University of Bonn, Bonn, Germany.
Elke MaesDepartment of Neonatology and Pediatric Intensive Care, Children's Hospital University of Bonn, Bonn, Germany.
Ursula Felderhoff-MüserDepartment of Pediatrics I, Neonatology and Experimental Perinatal Neurosciences, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Daniel PicardDivision of Pediatric Neuro-Oncogenomics, German Consortium for Translational Cancer Research (DKTK), Partner site Essen/Düsseldorf, Düsseldorf, Germany.
Hemmen SabirDepartment of Neonatology and Pediatric Intensive Care, Children's Hospital University of Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0002-4225-3554
University of Bonn · DEHeinrich Heine University Düsseldorf · DEUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxic-ischemic encephalopathy (HIE) mainly affects preterm and term newborns, leading to a high risk of brain damage. Coexisting infection/inflammation and birth asphyxia are key factors associated with intracerebral increase of proinflammatory cytokines linked to HIE. Microglia are key mediators of inflammation during perinatal brain injury, characterized by their phenotypic plasticity, which may facilitate their participation in both the progression and resolution of injury-induced inflammation. The purpose of this study was to investigate the temporal expression of genes associated with pro- and anti-inflammatory cytokines as well as the nucleotide-binding domain, leucine-rich repeat protein (NLRP-3) inflammasome from microglia cells. For this purpose, we used our established neonatal rat model of inflammation-sensitized hypoxic-ischemic (HI) brain injury in seven-day-old rats. We assessed gene expression profiles of 11 cytokines and for NLRP-3 using real-time PCR from sorted CD11b/c microglia of brain samples at different time points (3.5 h after LPS injection and 0, 5, 24, 48, and 72 hours post HI) following different treatments: vehicle,

Indexed as

AnimalsAnimals, NewbornBrain InjuriesDisease Models, AnimalFemaleHypoxia-Ischemia, BrainMicrogliaRatsRats, Wistar

Identifiers

PMID35281473
PMCPMC8906938
OpenAlexW4214846118

What Socratic holds

Textmetadata
LicenceCC BY
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.