Evidence map›Paper›PMID 32015413›Full record

ArticleScientific reports2020

Improved Calcium Homeostasis and Force by Selenium Treatment and Training in Aged Mouse Skeletal Muscle.

János Fodor, Dána Al-Gaadi, Tamás Czirják, Tamás Oláh, Beatrix Dienes, László Csernoch, Péter Szentesi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
  2. Review
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  7. Article
  8. Molecular Framework of the Onset and Progression of Skeletal Muscle Aging.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Reversing Decline in Aging Muscles: Expected Trends, Impacts and Remedies.Journal of functional morphology and kinesiology · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Ablation of skeletal muscle estrogen receptor alpha impairs contractility in male mice.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
    Article
  18. Article
  19. Article
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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

7 authors at 1 institution in 1 country.

János Fodor *Department of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Dána Al-Gaadi *Department of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Tamás CzirjákDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Tamás OláhDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID http://orcid.org/0000-0002-3834-6272
Beatrix DienesDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
László CsernochDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Péter SzentesiDepartment of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary. szentesi.peter@med.unideb.hu.ORCID http://orcid.org/0000-0003-2621-2282
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During aging reduction in muscle mass (sarcopenia) and decrease in physical activity lead to partial loss of muscle force and increased fatigability. Deficiency in the essential trace element selenium might augment these symptoms as it can cause muscle pain, fatigue, and proximal weakness. Average voluntary daily running, maximal twitch and tetanic force, and calcium release from the sarcoplasmic reticulum (SR) decreased while reactive oxygen species (ROS) production associated with tetanic contractions increased in aged - 22-month-old - as compared to young - 4-month-old - mice. These changes were accompanied by a decline in the ryanodine receptor type 1 (RyR1) and Selenoprotein N content and the increased amount of a degraded RyR1. Both lifelong training and selenium supplementation, but not the presence of an increased muscle mass at young age, were able to compensate for the reduction in muscle force and SR calcium release with age. Selenium supplementation was also able to significantly enhance the Selenoprotein N levels in aged mice. Our results describe, for the first time, the beneficial effects of selenium supplementation on calcium release from the SR and muscle force in old age while point out that increased muscle mass does not improve physical performance with aging.

Indexed as

AgingAnimalsCalciumDietary SupplementsHomeostasisHumansMiceMotor ActivityMuscle ContractionMuscle ProteinsMuscle, SkeletalRyanodine Receptor Calcium Release ChannelSarcopeniaSarcoplasmic ReticulumSeleniumSelenoproteinsCalciumMuscle Proteinsryanodine receptor 1, mouseRyanodine Receptor Calcium Release ChannelSeleniumSelenoproteinsSEPN1 protein, mouse

Identifiers

PMID32015413
PMCPMC6997352
OpenAlexW3004062245

What OpenQuestion holds

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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.