Evidence map›Paper›PMID 26624894›Full record

ArticlePloS one2015

Argon Mediates Anti-Apoptotic Signaling and Neuroprotection via Inhibition of Toll-Like Receptor 2 and 4.

Felix Ulbrich, Kai Kaufmann, Martin Roesslein, Franziska Wellner, Volker Auwärter, Jürgen Kempf, Torsten Loop, Hartmut Buerkle, Ulrich Goebel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  10. Argon Attenuates Multiorgan Failure in Relation with HMGB1 Inhibition.International journal of molecular sciences · 2021
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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

9 authors at 2 institutions in 1 country.

Felix UlbrichDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Kai KaufmannDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Martin RoessleinDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Franziska WellnerDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Volker AuwärterInstitute of Forensic Medicine, Forensic Toxicology, University of Freiburg, Freiburg, Germany.
Jürgen KempfInstitute of Forensic Medicine, Forensic Toxicology, University of Freiburg, Freiburg, Germany.
Torsten LoopDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Hartmut BuerkleDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
Ulrich GoebelDepartment of Anesthesiology and Intensive Care Medicine, University Medical Center, Freiburg, Germany.
University Medical Center Freiburg · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRecently, the noble gas argon attracted significant attention due to its neuroprotective properties. However, the underlying molecular mechanism is still poorly understood. There is growing evidence that the extracellular regulated kinase 1/2 (ERK1/2) is involved in Argon´s protective effect. We hypothesized that argon mediates its protective effects via the upstream located toll-like receptors (TLRs) 2 and 4.

methodsApoptosis in a human neuroblastoma cell line (SH-SY5Y) was induced using rotenone. Argon treatment was performed after induction of apoptosis with different concentrations (25, 50 and 75 Vol% in oxygen 21 Vol%, carbon dioxide and nitrogen) for 2 or 4 hours respectively. Apoptosis was analyzed using flow cytometry (annexin-V (AV)/propidiumiodide (PI)) staining, caspase-3 activity and caspase cleavage. TLR density on the cells' surface was analyzed using FACS and immunohistochemistry. Inhibition of TLR signaling and extracellular regulated kinase 1/2 (ERK1/2) were assessed by western blot, activity assays and FACS analysis.

resultsArgon 75 Vol% treatment abolished rotenone-induced apoptosis. This effect was attenuated dose- and time-dependently. Argon treatment was accompanied with a significant reduction of TLR2 and TLR4 receptor density and protein expression. Moreover, argon mediated increase in ERK1/2 phosphorylation was attenuated after inhibition of TLR signaling. ERK1/2 and TLR signaling inhibitors abolished the anti-apoptotic and cytoprotective effects of argon. Immunohistochemistry results strengthened these findings.

conclusionThese findings suggest that argon-mediated anti-apoptotic and neuroprotective effects are mediated via inhibition of TLR2 and TLR4.

Indexed as

ApoptosisArgonCaspase 3Cell Line, TumorHumansMAP Kinase Signaling SystemNeuroblastomaNeuroprotectionNeuroprotective AgentsPhosphorylationRotenoneSignal TransductionToll-Like Receptor 2Toll-Like Receptor 4ArgonCaspase 3Neuroprotective AgentsRotenoneTLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4

Identifiers

PMID26624894
PMCPMC4666627
OpenAlexW2186406222

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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.