Evidence map›Paper›PMID 28883493›Full record

ArticleScientific reports2017

Regulation of Akt-mTOR, ubiquitin-proteasome and autophagy-lysosome pathways in locomotor and respiratory muscles during experimental sepsis in mice.

Jérome Morel, Jean-Charles Palao, Josiane Castells, Marine Desgeorges, Thierry Busso, Serge Molliex, Vanessa Jahnke, Peggy Del Carmine, Julien Gondin, David Arnould and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Jérome MorelUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France. jerome.morel@chu-st-etienne.fr.
Jean-Charles PalaoUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Josiane CastellsUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Marine DesgeorgesUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Thierry BussoUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.ORCID 0000-0002-5042-4384
Serge MolliexDépartement d'anesthésie et réanimation, Centre Hospitalier Universitaire de Saint Etienne, Saint Etienne, France.
Vanessa JahnkeUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Peggy Del CarmineInstitut NeuroMyoGène, Université Claude Bernard Lyon 1, INSERM U1217, CNRS UMR 5310, Villeurbanne, France.
Julien GondinInstitut NeuroMyoGène, Université Claude Bernard Lyon 1, INSERM U1217, CNRS UMR 5310, Villeurbanne, France.
David ArnouldUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Anne Cécile DurieuxUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Damien FreyssenetUniv Lyon - University Jean Monnet Saint Etienne; Inter-university Laboratory of Human Movement, EA7424, F-42023, Saint Etienne, France.
Université Claude Bernard Lyon 1 · FRCentre Hospitalier Universitaire de Saint-Étienne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis induced loss of muscle mass and function contributes to promote physical inactivity and disability in patients. In this experimental study, mice were sacrificed 1, 4, or 7 days after cecal ligation and puncture (CLP) or sham surgery. When compared with diaphragm, locomotor muscles were more prone to sepsis-induced muscle mass loss. This could be attributed to a greater activation of ubiquitin-proteasome system and an increased myostatin expression. Thus, this study strongly suggests that the contractile activity pattern of diaphragm muscle confers resistance to atrophy compared to the locomotor gastrocnemius muscle. These data also suggest that a strategy aimed at preventing the activation of catabolic pathways and preserving spontaneous activity would be of interest for the treatment of patients with sepsis-induced neuromyopathy.

Indexed as

AutophagySignal TransductionAnimalsAtrophyBiomarkersCytokinesDiaphragmDisease Models, AnimalInflammation MediatorsLysosomesMaleMicePhosphorylationProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktSepsisBiomarkersCytokinesInflammation MediatorsProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesUbiquitin

Identifiers

PMID28883493
PMCPMC5589872
OpenAlexW2753206310

What OpenQuestion 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 OpenQuestion graph.