Evidence map›Paper›PMID 40193354›Full record

ArticlePloS one2025

A novel ex vivo protocol that mimics length and excitation changes of human muscles during walking induces force losses in EDL but not in soleus of mdx mice.

Xiao Hu, Allison N McCrady, Katherine E Bukovec, Claire Yuan, Emily Y Miller, Rachel K Bour, Anthony C Bruce, Katherine B Crump, Shayn M Peirce, Robert W Grange and 1 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Xiao HuDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0001-9633-1450
Allison N McCradyDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Katherine E BukovecDepartment of Human Nutrition, Foods, and Exercise and Metabolism Core, Virginia Tech, Blacksburg, Virginia, United States of America.
Claire YuanDepartment of Human Nutrition, Foods, and Exercise and Metabolism Core, Virginia Tech, Blacksburg, Virginia, United States of America.
Emily Y MillerDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Rachel K BourDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Anthony C BruceDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Katherine B CrumpDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Shayn M PeirceDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.
Robert W GrangeDepartment of Human Nutrition, Foods, and Exercise and Metabolism Core, Virginia Tech, Blacksburg, Virginia, United States of America.
Silvia S BlemkerDepartment of Biomedical Engineering, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0002-2019-1153

Funding

Multiscale Modeling for Treatment Discovery in Duchenne Muscular DystrophyU01AR069393 · NIAMS · UNIVERSITY OF VIRGINIA · PI BLEMKER, SILVIA SALINAS, PEIRCE-COTTLER, SHAYN · 2016 to 2020
$2.5M
NIAMS NIH HHS U01 AR069393
6 · The paper itself

Abstract

Although eccentric contraction protocols are widely used to study the pathophysiology and potential treatments for Duchenne muscular dystrophy (DMD), they do not reflect the stresses, strains, strain rates, and excitation profiles that DMD muscles experience during human daily functional tasks, like walking. This limitation of eccentric contractions may impede our understanding of disease progression in DMD and proper assessment of treatment efficacy. The goals of this study were to examine the extent of force loss induced by a gait cycling protocol we developed, and compare to that from a typical eccentric contraction protocol in soleus and extensor digitorum longus (EDL) muscles of mdx mice. To achieve this goal, mdx soleus and EDL muscles were subjected to eccentric contractions at three levels of strain (10%, 20% and 30% optimal length Lo) and up to 200 cycles of our gait cycling protocol that mimicked the length changes and excitation patterns of the corresponding muscles during human walking gait. Our results showed that EDL but not soleus muscles had significant losses in isometric tetanic forces after the cycling protocols. Compared to the eccentric contraction protocol, the decrements in contractile performance from the cycling protocol were similar to those from the eccentric contractions at 10% in soleus and 20% Lo in EDL. Together, these results indicated the gait cycling protocol is a valuable experimental approach to better understand disease progression and to screen and evaluate efficacy of novel therapeutics for DMD.

Indexed as

Muscle ContractionMuscle, SkeletalMuscular Dystrophy, DuchenneWalkingAnimalsGaitHumansMaleMiceMice, Inbred mdx

Identifiers

PMID40193354
PMCPMC11975108

What OpenQuestion holds

Textmetadata
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.