Evidence map›Paper›PMID 29470148›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2018

Voluntary wheel running increases satellite cell abundance and improves recovery from disuse in gastrocnemius muscles from mice.

Matthew J Brooks, Ameena Hajira, Junaith S Mohamed, Stephen E Alway

Open access · bronzeAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
1.8field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 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

4 authors at 1 institution in 1 country.

Matthew J BrooksLaboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, Department of Human Performance and Applied Exercise Science, West Virginia University School of Medicine , Morgantown, West Virginia.
Ameena HajiraLaboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, Department of Human Performance and Applied Exercise Science, West Virginia University School of Medicine , Morgantown, West Virginia.
Junaith S MohamedLaboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, Department of Human Performance and Applied Exercise Science, West Virginia University School of Medicine , Morgantown, West Virginia.
Stephen E AlwayLaboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, Department of Human Performance and Applied Exercise Science, West Virginia University School of Medicine , Morgantown, West Virginia.
West Virginia University · US

Funding

WVU &MU NEW FACULTY GRANTSP20RR016477 · NCRR · MARSHALL UNIVERSITY · PI RANKIN, GARY O · 2001 to 2011
$35.5M
West Virginia University Stroke COBREP20GM109098 · NIGMS · WEST VIRGINIA UNIVERSITY · PI HRUSKA, MARTIN · 2014 to 2024
$24.5M
THE ROLE OF HEF1 PROTEIN IN INVASION OF METASTATIC BREAST CANCERP20RR016440 · NCRR · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2001 to 2010
$22.8M
West Virginia Flow Cytometry Core FacilityP30GM103488 · NIGMS · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2012 to 2016
$4.8M
NCRR NIH HHS P20 RR016440NCRR NIH HHS P20 RR016477NIGMS NIH HHS P20 GM109098NIGMS NIH HHS P30 GM103488
6 · The paper itself

Abstract

Reloading of atrophied muscles after hindlimb suspension unloading (HSU) can induce injury and prolong recovery. Low-impact exercise, such as voluntary wheel running, has been identified as a nondamaging rehabilitation therapy in rodents, but its effects on muscle function, morphology, and satellite cell activity after HSU are unclear. This study tested the hypothesis that low-impact wheel running would increase satellite cell proliferation and improve recovery of muscle structure and function after HSU in mice. Young adult male and female C57BL/6 mice ( n = 6/group) were randomly placed into five groups. These included HSU without recovery (HSU), normal ambulatory recovery for 14 days after HSU (HSU+NoWR), and voluntary wheel running recovery for 14 days after HSU (HSU+WR). Two control groups were used: nonsuspended mouse cage controls (Control) and voluntary wheel running controls (ControlWR). Satellite cell activation was evaluated by providing mice 5-bromo-2'-deoxyuridine (BrdU) in their drinking water. As expected, HSU significantly reduced in vivo maximal force, decreased in vivo fatigability, and decreased type I and IIa myosin heavy chain (MHC) abundance in plantarflexor muscles. HSU+WR mice significantly improved plantarflexor fatigue resistance, increased type I and IIa MHC abundance, increased fiber cross-sectional area, and increased the percentage of type I and IIA muscle fibers in the gastrocnemius muscle. HSU+WR mice also had a significantly greater percentage of BrdU-positive and Pax 7-positive nuclei inside muscle fibers and a greater MyoD-to-Pax 7 protein ratio compared with HSU+NoWR mice. The mechanotransduction protein Yes-associated protein (YAP) was elevated with reloading after HSU, but HSU+WR mice had lower levels of the inactive phosphorylated YAP

Indexed as

Recovery of FunctionAdaptor Proteins, Signal TransducingAnimalsCell Cycle ProteinsCell ProliferationFemaleHindlimb SuspensionHippo Signaling PathwayMaleMice, Inbred C57BLMuscle, SkeletalPhosphoproteinsProtein Serine-Threonine KinasesRandom AllocationRunningSatellite Cells, Skeletal MuscleAdaptor Proteins, Signal TransducingCell Cycle ProteinsPhosphoproteinsProtein Serine-Threonine KinasesYap1 protein, mouseYAP-Signaling Proteinsatrophyfatiguemuscle disusemuscle fibersrunning exercisesatellite cellsYes-associated protein

Identifiers

PMID29470148
PMCPMC6032091
OpenAlexW2788065557

What OpenQuestion holds

Textmetadata
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.