Evidence map›Paper›PMID 25907787›Full record

ArticlePhysiological reports2015

Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice.

Erick O Hernández-Ochoa, Stephen J P Pratt, Karla P Garcia-Pelagio, Martin F Schneider, Richard M Lovering

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Twisting Paths: The Paradox of Fiber Branching in Muscle Regeneration.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Lymphatic dysfunction is linked to disease pathogenesis in Duchenne muscular dystrophy animal models.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Voltage sensor movements of CaProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Lifespan Analysis of DystrophicFrontiers in physiology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Altered nuclear dynamics in MDX myofibers.Journal of applied physiology (Bethesda, Md. : 1985) · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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

5 authors at 1 institution in 1 country.

Erick O Hernández-OchoaDepartment of Biochemistry & Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland.
Stephen J P PrattDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, Maryland.
Karla P Garcia-PelagioDepartment of Physiology, University of Maryland School of Medicine, Baltimore, Maryland.
Martin F SchneiderDepartment of Biochemistry & Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland.
Richard M LoveringDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, Maryland rlovering@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

Roles of voltage sensor, S100A1 and calmodulin in skeletal muscle Ca2+ signalingR37AR055099 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHNEIDER, MARTIN F · 2012 to 2021
$3.5M
NIAMS NIH HHS R37 AR055099
6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD), the most common and severe muscular dystrophy, is caused by the absence of dystrophin. Muscle weakness and fragility (i.e., increased susceptibility to damage) are presumably due to structural instability of the myofiber cytoskeleton, but recent studies suggest that the increased presence of malformed/branched myofibers in dystrophic muscle may also play a role. We have previously studied myofiber morphology in healthy wild-type (WT) and dystrophic (MDX) skeletal muscle. Here, we examined myofiber excitability using high-speed confocal microscopy and the voltage-sensitive indicator di-8-butyl-amino-naphthyl-ethylene-pyridinium-propyl-sulfonate (di-8-ANEPPS) to assess the action potential (AP) properties. We also examined AP-induced Ca(2+) transients using high-speed confocal microscopy with rhod-2, and assessed sarcolemma fragility using elastimetry. AP recordings showed an increased width and time to peak in malformed MDX myofibers compared to normal myofibers from both WT and MDX, but no significant change in AP amplitude. Malformed MDX myofibers also exhibited reduced AP-induced Ca(2+) transients, with a further Ca(2+) transient reduction in the branches of malformed MDX myofibers. Mechanical studies indicated an increased sarcolemma deformability and instability in malformed MDX myofibers. The data suggest that malformed myofibers are functionally different from myofibers with normal morphology. The differences seen in AP properties and Ca(2+) signals suggest changes in excitability and remodeling of the global Ca(2+) signal, both of which could underlie reported weakness in dystrophic muscle. The biomechanical changes in the sarcolemma support the notion that malformed myofibers are more susceptible to damage. The high prevalence of malformed myofibers in dystrophic muscle may contribute to the progressive strength loss and fragility seen in dystrophic muscles.

Indexed as

Action potentialanimal model of muscular dystrophyCa2+ indicatorCa2+ transientsdi‐8‐ANEPPSDuchenne muscular dystrophyelastimetryMDXmyofiber branchingsarcolemma biomechanicsT‐tubule morphologyvoltage‐sensitive dye

Identifiers

PMID25907787
PMCPMC4425971
OpenAlexW2143370070

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.