Evidence map›Paper›PMID 33004706›Full record

ArticleMedical gas research

Argon treatment after experimental subarachnoid hemorrhage: evaluation of microglial activation and neuronal survival as a subanalysis of a randomized controlled animal trial.

Benedikt Kremer, Mark Coburn, Agnieszka Weinandy, Kay Nolte, Hans Clusmann, Michael Veldeman, Anke Höllig

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Medical gas research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  7. Article
  8. Neuroprotective Strategies in Aneurysmal Subarachnoid Hemorrhage (aSAH).International journal of molecular sciences · 2021
    Review
  9. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Benedikt KremerDepartment of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany.
Mark CoburnDepartment of Anaesthesiology, RWTH Aachen University Hospital, Aachen, Germany.
Agnieszka WeinandyDepartment of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany.
Kay NolteInstitute of Neuropathology, RWTH Aachen University Hospital, Aachen, Germany.
Hans ClusmannDepartment of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany.
Michael VeldemanDepartment of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany.
Anke HölligDepartment of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany.
Universitätsklinikum Aachen · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereinafter, we evaluate argon's neuroprotective and immunomodulatory properties after experimental subarachnoid hemorrhage (SAH) examining various localizations (hippocampal and cortical regions) with respect to neuronal damage and microglial activation 6, 24 and 72 hours after SAH. One hour after SAH (endovascular perforation rat model) or sham surgery, a mixture of gas containing 50% argon (argon group) or 50% nitrogen (control group) was applied for 1 hour. At 6 hours after SAH, argon reduced neuronal damage in the hippocampal regions in the argon group compared to the control group (P < 0.034). Hippocampal microglial activation did not differ between the treatment groups over time. The basal cortical regions did not show a different lesion pattern, but microglial activation was significantly reduced in the argon group 72 hours after SAH (P = 0.034 vs. control group). Whereas callosal microglial activation was significantly reduced at 24 hours in the argon-treated group (P = 0.018). Argon treatment ameliorated only early hippocampal neuronal damage after SAH. Inhibition of microglial activation was seen in some areas later on. Thus, argon may influence the microglial inflammatory response and neuronal survival after SAH; however, due to low sample sizes the interpretation of our results is limited. The study protocol was approved by the Government Agency for Animal Use and Protection (Protocol number: TVA 10416G1; initially approved by the "Landesamt für Natur, Umwelt und Verbraucherschutz NRW," Recklinghausen, Germany, on April 28, 2009).

Indexed as

AnimalsArgonCalcium-Binding ProteinsDisease Models, AnimalGermanyHippocampusMaleMicrofilament ProteinsMicrogliaNeuronsNeuroprotective AgentsRandomized Controlled Trials as TopicRatsRats, Sprague-DawleySubarachnoid HemorrhageTime FactorsAIF1 protein, humanArgonCalcium-Binding ProteinsMicrofilament ProteinsNeuroprotective Agentsargonearly brain injuryexperimental subarachnoid hemorrhageIba-1microglial activationneuroinflammationneuronal survivalneuroprotection

Identifiers

PMID33004706
PMCPMC8086619
OpenAlexW3088501244

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.