Evidence map›Paper›PMID 25535961›Full record

ArticlePloS one2014

Argon inhalation attenuates retinal apoptosis after ischemia/reperfusion injury in a time- and dose-dependent manner in rats.

Felix Ulbrich, Nils Schallner, Mark Coburn, Torsten Loop, Wolf Alexander Lagrèze, Julia Biermann, Ulrich Goebel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. CardioPulmonary resuscitation withResuscitation plus · 2025
    Article
  5. Review
  6. Positive Effects of Argon Inhalation After Traumatic Brain Injury in Rats.International journal of molecular sciences · 2024
    Article
  7. Article
  8. Review
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  11. Article
  12. Article
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  14. Article
  15. Article
  16. Article
  17. Article
  18. The Molecular Pathway of Argon-Mediated Neuroprotection.International journal of molecular sciences · 2016
    Review
  19. Carbon monoxide treatment reduces microglial activation in the ischemic rat retina.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2016
    Article
  20. 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 1 country.

Felix UlbrichDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Nils SchallnerDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Mark CoburnDepartment of Anesthesiology, University Hospital RWTH Aachen, Aachen, Germany.
Torsten LoopDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Wolf Alexander LagrèzeEye Center, University Medical Center, Freiburg, Germany.
Julia BiermannEye Center, University Medical Center, Freiburg, Germany.
Ulrich GoebelDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
University Medical Center Freiburg · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRetinal ischemia and reperfusion injuries (IRI) permanently affect neuronal tissue and function by apoptosis and inflammation due to the limited regenerative potential of neurons. Recently, evidence emerged that the noble gas Argon exerts protective properties, while lacking any detrimental or adverse effects. We hypothesized that Argon inhalation after IRI would exert antiapoptotic effects in the retina, thereby protecting retinal ganglion cells (RGC) of the rat's eye.

methodsIRI was performed on the left eyes of rats (n = 8) with or without inhaled Argon postconditioning (25, 50 and 75 Vol%) for 1 hour immediately or delayed after ischemia (i.e. 1.5 and 3 hours). Retinal tissue was harvested after 24 hours to analyze mRNA and protein expression of Bcl-2, Bax and Caspase-3, NF-κB. Densities of fluorogold-prelabeled RGCs were analyzed 7 days after injury in whole-mounts. Histological tissue samples were prepared for immunohistochemistry and blood was analyzed regarding systemic effects of Argon or IRI. Statistics were performed using One-Way ANOVA.

resultsIRI induced RGC loss was reduced by Argon 75 Vol% inhalation and was dose-dependently attenuated by lower concentrations, or by delayed Argon inhalation (1504±300 vs. 2761±257; p<0.001). Moreover, Argon inhibited Bax and Bcl-2 mRNA expression significantly (Bax: 1.64±0.30 vs. 0.78±0.29 and Bcl-2: 2.07±0.29 vs. 0.99±0.22; both p<0.01), as well as caspase-3 cleavage (1.91±0.46 vs. 1.05±0.36; p<0.001). Expression of NF-κB was attenuated significantly. Immunohistochemistry revealed an affection of Müller cells and astrocytes. In addition, IRI induced leukocytosis was reduced significantly after Argon inhalation at 75 Vol%.

conclusionImmediate and delayed Argon postconditioning protects IRI induced apoptotic loss of RGC in a time- and dose-dependent manner, possibly mediated by the inhibition of NF-κB. Further studies need to evaluate Argon's possible role as a therapeutic option.

Indexed as

Administration, InhalationAnimalsApoptosisArgonbcl-2-Associated X ProteinCaspase 3FemaleGene Expression Regulation, NeoplasticMaleProto-Oncogene Proteins c-bcl-2RatsRats, Sprague-DawleyReperfusion InjuryRetinaRNA, MessengerArgonbcl-2-Associated X ProteinCaspase 3Proto-Oncogene Proteins c-bcl-2RNA, Messenger

Identifiers

PMID25535961
PMCPMC4275290
OpenAlexW1998665003

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.