Evidence map›Paper›PMID 35025912›Full record

ArticlePloS one2022

Effect of short-term hindlimb immobilization on skeletal muscle atrophy and the transcriptome in a low compared with high responder to endurance training model.

Jamie-Lee M Thompson, Daniel W D West, Thomas M Doering, Boris P Budiono, Sarah J Lessard, Lauren G Koch, Steven L Britton, Nuala M Byrne, Matthew A Brown, Kevin J Ashton and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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  5. Article
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

11 authors at 8 institutions in 4 countries.

Jamie-Lee M ThompsonFaculty of Health Sciences and Medicine, Bond University, Robina, Australia.
Daniel W D WestDepartment of Physiology and Membrane Biology, University of California, Davis, Davis, California, United States of America.
Thomas M DoeringFaculty of Health Sciences and Medicine, Bond University, Robina, Australia.ORCID 0000-0002-6427-1067
Boris P BudionoSchool of Community Health, Charles Sturt University, Bathurst, Australia.ORCID 0000-0002-1189-739X
Sarah J LessardResearch Division, Joslin Diabetes Center, Boston, Massachusetts, United States of America.
Lauren G KochDepartment of Physiology and Pharmacology, The University of Toledo College of Medicine and Life Sciences, Toledo, Ohio, United States of America.
Steven L BrittonDepartment of Anesthesiology, University of Michigan, Ann Arbor, Michigan, United States of America.
Nuala M ByrneSchool of Health Sciences, University of Tasmania, Hobart, Australia.
Matthew A BrownNational Institute for Health Research, Guy's and St Thomas' Biomedical Research Centre, Kings College London, London, United Kingdom.
Kevin J AshtonFaculty of Health Sciences and Medicine, Bond University, Robina, Australia.
Vernon G CoffeyFaculty of Health Sciences and Medicine, Bond University, Robina, Australia.ORCID 0000-0001-6837-1906
Bond University · AUBrigham and Women's Hospital · USCharles Sturt University · AUKing's College London · GBUniversity of Michigan · USUniversity of Tasmania · AUUniversity of Toledo · USUniversity of Toronto · CA

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
NIH HHS P40 OD021331
6 · The paper itself

Abstract

Skeletal muscle atrophy is a physiological response to disuse, aging, and disease. We compared changes in muscle mass and the transcriptome profile after short-term immobilization in a divergent model of high and low responders to endurance training to identify biological processes associated with the early atrophy response. Female rats selectively bred for high response to endurance training (HRT) and low response to endurance training (LRT; n = 6/group; generation 19) underwent 3 day hindlimb cast immobilization to compare atrophy of plantaris and soleus muscles with line-matched controls (n = 6/group). RNA sequencing was utilized to identify Gene Ontology Biological Processes with differential gene set enrichment. Aerobic training performed prior to the intervention showed HRT improved running distance (+60.6 ± 29.6%), while LRT were unchanged (-0.3 ± 13.3%). Soleus atrophy was greater in LRT vs. HRT (-9.0 ±8.8 vs. 6.2 ±8.2%; P<0.05) and there was a similar trend in plantaris (-16.4 ±5.6% vs. -8.5 ±7.4%; P = 0.064). A total of 140 and 118 biological processes were differentially enriched in plantaris and soleus muscles, respectively. Soleus muscle exhibited divergent LRT and HRT responses in processes including autophagy and immune response. In plantaris, processes associated with protein ubiquitination, as well as the atrogenes (Trim63 and Fbxo32), were more positively enriched in LRT. Overall, LRT demonstrate exacerbated atrophy compared to HRT, associated with differential gene enrichments of biological processes. This indicates that genetic factors that result in divergent adaptations to endurance exercise, may also regulate biological processes associated with short-term muscle unloading.

Indexed as

Adaptation, PhysiologicalAnimalsEndurance TrainingExercise TherapyFemaleGenomic LibraryHindlimb SuspensionHumansMaleMuscle, SkeletalMuscular AtrophyPhysical Conditioning, AnimalRatsSequence Analysis, RNATranscriptome

Identifiers

PMID35025912
PMCPMC8757917
OpenAlexW4206714171

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.