Evidence map›Paper›PMID 35774589›Full record

ArticleFunction (Oxford, England)2022

Muscle-Specific Cellular and Molecular Adaptations to Late-Life Voluntary Concurrent Exercise.

Cory M Dungan, Camille R Brightwell, Yuan Wen, Christopher J Zdunek, Christine M Latham, Nicholas T Thomas, Alyaa M Zagzoog, Benjamin D Brightwell, Georgia L VonLehmden, Alexander R Keeble and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Function (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

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  19. Article
  20. DNA Methylation in the Adaptive Response to Exercise.Sports medicine (Auckland, N.Z.) · 2024
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Cory M DunganDepartment of Physical Therapy, University of Kentucky, Lexington 40536, KY, USA.
Camille R BrightwellCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Yuan WenDepartment of Physical Therapy, University of Kentucky, Lexington 40536, KY, USA.
Christopher J ZdunekCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Christine M LathamCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Nicholas T ThomasCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Alyaa M ZagzoogCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Benjamin D BrightwellKinesiology and Health Promotion Graduate Program, University of Kentucky, Lexington 40536, KY, USA.
Georgia L VonLehmdenCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Alexander R KeebleCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.
Stanley J WatowichDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston 77555, TX, USA.
Kevin A MurachCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.ORCID 0000-0003-2783-7137
Christopher S FryCenter for Muscle Biology, University of Kentucky, Lexington 40536, KY, USA.

Funding

Exercise-induced skeletal muscle exosomes promote adipocyte lipolysisR01DK119619 · NIDDK · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, PETERSON, CHARLOTTE A. · 2018 to 2022
$2.3M
The role of satellite cells in skeletal muscle hypertrophy with agingR01AG069909 · NIA · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, WEN, YUAN · 2021 to 2025
$2.1M
Myonuclear Epigenetics of Skeletal Muscle Mass Regulation with AgeR00AG063994 · NIA · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI MURACH, KEVIN · 2021 to 2023
$735k
Development of NNMT inhibitors as novel interventions to activate quiescent muscle stem cells and improve age-related muscle degenerationR21AG063056 · NIA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WATOWICH, STANLEY J · 2019 to 2020
$435k
NIA NIH HHS R00 AG063994NIA NIH HHS R01 AG069909NIA NIH HHS R21 AG063056NIDDK NIH HHS R01 DK119619
6 · The paper itself

Abstract

Murine exercise models can provide information on factors that influence muscle adaptability with aging, but few translatable solutions exist. Progressive weighted wheel running (PoWeR) is a simple, voluntary, low-cost, high-volume endurance/resistance exercise approach for training young mice. In the current investigation, aged mice (22-mo-old) underwent a modified version of PoWeR for 8 wk. Muscle functional, cellular, biochemical, transcriptional, and myonuclear DNA methylation analyses provide an encompassing picture of how muscle from aged mice responds to high-volume combined training. Mice run 6-8 km/d, and relative to sedentary mice, PoWeR increases plantarflexor muscle strength. The oxidative soleus of aged mice responds to PoWeR similarly to young mice in every parameter measured in previous work; this includes muscle mass, glycolytic-to-oxidative fiber type transitioning, fiber size, satellite cell frequency, and myonuclear number. The oxidative/glycolytic plantaris adapts according to fiber type, but with modest overall changes in muscle mass. Capillarity increases markedly with PoWeR in both muscles, which may be permissive for adaptability in advanced age. Comparison to published PoWeR RNA-sequencing data in young mice identified conserved regulators of adaptability across age and muscles; this includes

Indexed as

Muscle Fibers, SkeletalPhysical Conditioning, AnimalAdaptation, PhysiologicalAnimalsMiceMotor ActivityMuscle, Skeletalcapillarizationconcurrent trainingDNA methylationhypertrophysarcopeniaskeletal muscle

Identifiers

PMID35774589
PMCPMC9233305

What OpenQuestion holds

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LicenceCC BY-NC
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.