Evidence map›Paper›PMID 38660728›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2024

Persistent neuroinflammation and functional deficits in a murine model of decompression sickness.

Abid R Bhat, Awadhesh K Arya, Veena M Bhopale, Zuha Imtiyaz, Su Xu, Dilara Bedir, Stephen R Thom

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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 2 countries.

Abid R BhatDepartment of Emergency Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.ORCID 0000-0003-4476-1189
Awadhesh K AryaDepartment of Emergency Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.ORCID 0000-0002-2142-4924
Veena M BhopaleDepartment of Emergency Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.
Zuha ImtiyazDepartment of Emergency Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.
Su XuDepartment of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.
Dilara BedirDepartment of Undersea and Hyperbaric Medicine, Gulhane Education and Research Hospital, Istanbul, Turkey.
Stephen R ThomDepartment of Emergency Medicine, University of Maryland School of Medicine, Baltimore, Maryland, United States.ORCID 0000-0002-3533-6124
University of Maryland, Baltimore · USGülhane Askerî Tıp Akademisi · TR

Funding

Inflammatory changes and glymphatic dysfunction in carbon monoxide neuropathologyR01NS122855 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI STEPHEN RAYMOND THOM · 2022 to 2026
$2.9M
DOD | USN | Office of Naval Research (ONR) N00014-22-1-2818HHS | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01-NS-122855NINDS NIH HHS R01 NS122855
6 · The paper itself

Abstract

We hypothesized that early intra-central nervous system (CNS) responses in a murine model of decompression sickness (DCS) would be reflected by changes in the microparticles (MPs) that exit the brain via the glymphatic system, and due to systemic responses the MPs would cause inflammatory changes lasting for many days leading to functional neurological deficits. Elevations on the order of threefold of blood-borne inflammatory MPs, neutrophil activation, glymphatic flow, and neuroinflammation in cerebral cortex and hippocampus were found in mice at 12 days after exposure to 760 kPa of air for 2 h. Mice also exhibited a significant decline in memory and locomotor activity, as assessed by novel object recognition and rotarod testing. Similar inflammatory changes in blood, neuroinflammation, and functional impairments were initiated in naïve mice by injection of filamentous (F-) actin-positive MPs, but not F-actin-negative MPs, obtained from decompressed mice. We conclude that high pressure/decompression stress establishes a systemic inflammatory process that results in prolonged neuroinflammation and functional impairments in the mouse decompression model.

Indexed as

Decompression SicknessDisease Models, AnimalMice, Inbred C57BLNeuroinflammatory DiseasesAnimalsCell-Derived MicroparticlesCerebral CortexGlymphatic SystemHippocampusInflammationMaleMiceNeutrophil Activationastrocytesdecompressionmicrogliamicroparticlesneutrophil activation

Identifiers

PMID38660728
PMCPMC11389893
OpenAlexW4395463457

What OpenQuestion holds

Textmetadata
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.