Evidence map›Paper›PMID 30538258›Full record

ArticleScientific reports2018

Differential regulation of cysteine oxidative post-translational modifications in high and low aerobic capacity.

Rodrigo W A Souza, Christiano R R Alves, Alessandra Medeiros, Natale Rolim, Gustavo J J Silva, José B N Moreira, Marcia N Alves, Martin Wohlwend, Mohammed Gebriel, Lars Hagen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 23 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

16 authors at 7 institutions in 4 countries.

Rodrigo W A SouzaSchool of Physical Education and Sport, University of São Paulo, São Paulo, Brazil. rodrigowas@usp.br.
Christiano R R AlvesSchool of Physical Education and Sport, University of São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-2646-9689
Alessandra MedeirosBiosciences Department, Federal University of São Paulo, Santos, Brazil.
Natale RolimK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Gustavo J J SilvaK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
José B N MoreiraK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Marcia N AlvesK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Martin WohlwendK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Mohammed GebrielDepartment of Cancer Research and Molecular Medicine and PROMEC Core Facility for Proteomics and Modomics, Norwegian University of Science and Technology (NTNU), and Central Norway Regional Health Authority, Trondheim, Norway.
Lars HagenDepartment of Cancer Research and Molecular Medicine and PROMEC Core Facility for Proteomics and Modomics, Norwegian University of Science and Technology (NTNU), and Central Norway Regional Health Authority, Trondheim, Norway.
Animesh SharmaDepartment of Cancer Research and Molecular Medicine and PROMEC Core Facility for Proteomics and Modomics, Norwegian University of Science and Technology (NTNU), and Central Norway Regional Health Authority, Trondheim, Norway.ORCID http://orcid.org/0000-0002-8791-4635
Lauren G KochDepartment of Physiology & Pharmacology, The University of Toledo, Toledo, Ohio, USA.
Steven L BrittonDepartment of Anesthesiology, University of Michigan - Medical School, Ann Arbor, Michigan, USA.
Geir SlupphaugDepartment of Cancer Research and Molecular Medicine and PROMEC Core Facility for Proteomics and Modomics, Norwegian University of Science and Technology (NTNU), and Central Norway Regional Health Authority, Trondheim, Norway.
Ulrik WisløffK.G. Jebsen Center of Exercise in Medicine, Department of Circulation and Medical Imaging, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Patricia C BrumSchool of Physical Education and Sport, University of São Paulo, São Paulo, Brazil. pcbrum@usp.br.ORCID http://orcid.org/0000-0002-4750-6506
Norwegian University of Science and Technology · NOUniversidade de São Paulo · BRJoslin Diabetes Center · USThe University of Queensland · AUUniversidade Federal de São Paulo · BRUniversity of Michigan · USUniversity of Toledo · US

Funding

Resource for Rat Genetic Models of Aerobic CapacityP40OD021331 · OD · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI KOCH, LAUREN GERARD · 2015 to 2019
$1.9M
Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 12/25240-1, 14/03016-8Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 14/25957-9Fundação de Amparo à Pesquisa do Estado de São Paulo (São Paulo Research Foundation) 2015/22814-5Ministry of Science, Technology and Innovation | Conselho Nacional de Desenvolvimento Científico e Tecnológico (National Council for Scientific and Technological Development) 306261/2016-2NIH HHS P40 OD021331
6 · The paper itself

Abstract

Given the association between high aerobic capacity and the prevention of metabolic diseases, elucidating the mechanisms by which high aerobic capacity regulates whole-body metabolic homeostasis is a major research challenge. Oxidative post-translational modifications (Ox-PTMs) of proteins can regulate cellular homeostasis in skeletal and cardiac muscles, but the relationship between Ox-PTMs and intrinsic components of oxidative energy metabolism is still unclear. Here, we evaluated the Ox-PTM profile in cardiac and skeletal muscles of rats bred for low (LCR) and high (HCR) intrinsic aerobic capacity. Redox proteomics screening revealed different cysteine (Cys) Ox-PTM profile between HCR and LCR rats. HCR showed a higher number of oxidized Cys residues in skeletal muscle compared to LCR, while the opposite was observed in the heart. Most proteins with differentially oxidized Cys residues in the skeletal muscle are important regulators of oxidative metabolism. The most oxidized protein in the skeletal muscle of HCR rats was malate dehydrogenase (MDH1). HCR showed higher MDH1 activity compared to LCR in skeletal, but not cardiac muscle. These novel findings indicate a clear association between Cys Ox-PTMs and aerobic capacity, leading to novel insights into the role of Ox-PTMs as an essential signal to maintain metabolic homeostasis.

Indexed as

AnimalsCell RespirationCysteineEnergy MetabolismExercise ToleranceMalate DehydrogenaseMaleMuscle, SkeletalMyocardiumOxidation-ReductionOxidative StressPhysical Conditioning, AnimalPhysical EnduranceProtein Processing, Post-TranslationalRatsRunningCysteineMalate Dehydrogenase

Identifiers

PMID30538258
PMCPMC6289973
OpenAlexW2902460706

What OpenQuestion holds

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LicenceCC BY
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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.