Evidence map›Paper›PMID 31866157›Full record

ArticleNeurobiology of aging2020

Neuromuscular junction transmission failure is a late phenotype in aging mice.

Deepti Chugh, Chitra C Iyer, Xueyong Wang, Prameela Bobbili, Mark M Rich, W David Arnold

Open access · greenAbstract read
In one paragraph

Article in Neurobiology of aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. The Neuromuscular Junction: A Shared Vulnerability in Aging and Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  9. 5-HTGeroScience · 2025
    Article
  10. MuSK Regulates Neuromuscular Junction Nav1.4 Localization and Excitability.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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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

6 authors at 2 institutions in 1 country.

Deepti ChughDepartment of Neurology, Neuromuscular Division, The Ohio State University, Wexner Medical Center, Columbus, OH, USA.
Chitra C IyerDepartment of Neurology, Neuromuscular Division, The Ohio State University, Wexner Medical Center, Columbus, OH, USA.
Xueyong WangDepartment of Neuroscience, Cell Biology, and Physiology Wright State University, Dayton, OH, USA.
Prameela BobbiliDepartment of Neurology, Neuromuscular Division, The Ohio State University, Wexner Medical Center, Columbus, OH, USA.
Mark M RichDepartment of Neuroscience, Cell Biology, and Physiology Wright State University, Dayton, OH, USA.
W David ArnoldDepartment of Neurology, Neuromuscular Division, The Ohio State University, Wexner Medical Center, Columbus, OH, USA; Department of Physical Medicine and Rehabilitation, The Ohio State University, Wexner Medical Center, Columbus, OH, USA; Department of Neuroscience, The Ohio State University, Wexner Medical Center, Columbus, OH, USA; Department of Physiology and Cell Biology, The Ohio State University, Wexner Medical Center, Columbus, OH, USA. Electronic address: william.arnold@osumc.edu.
The Ohio State University Wexner Medical Center · USWright State University · US

Funding

Novel Approaches to Therapy of Muscle Ion ChannelopathiesR01AR074985 · NIAMS · WRIGHT STATE UNIVERSITY · PI MARK M RICH · 2019 to 2026
$3.9M
The Role of SMN in Aging Related Weakness: A Novel Therapeutic TargetR56AG055795 · NIA · OHIO STATE UNIVERSITY · PI ARNOLD, WILLIAM DAVID · 2019 to 2019
$504k
Sarcopenia and the motor neuronR03AG050877 · NIA · OHIO STATE UNIVERSITY · PI ARNOLD, WILLIAM DAVID · 2016 to 2017
$231k
NIAMS NIH HHS R01 AR074985NIA NIH HHS R03 AG050877NIA NIH HHS R56 AG055795
6 · The paper itself

Abstract

Neurodegeneration has increasingly been considered an important factor in the pathogenesis of sarcopenia or age-related loss of muscle mass and strength. Experiments were designed to investigate the fidelity of neuromuscular junction (NMJ) transmission across the lifespan in hindlimb muscles of male and female C57BL/6J mice (at 12, 20, 24, 27, and 29 months of age). Single-fiber electromyography recordings demonstrated abrupt onset of NMJ transmission failure at 27 months of age. Failed NMJ transmission was a later onset phenotype as compared with other assessments of motor unit numbers, muscle contractility, and frailty which showed alterations at 20 months of age. Ex vivo NMJ recordings demonstrated no reduction of endplate current amplitude in support of reduced muscle fiber excitability as the cause of failed NMJ transmission in aged mice. Improved understanding of age-related neurodegeneration will likely have important implications in designing novel therapeutic interventions specific for different stages of sarcopenia. Our findings suggest reduced muscle excitability may be a potential therapeutic target for improvement of physical function in older adults.

Indexed as

PhenotypeAgingAnimalsFemaleMaleMice, Inbred C57BLMuscle ContractionMuscle, SkeletalNeuromuscular JunctionSarcopeniaAgingFrailtyMotor unitNeuromuscular junctionSarcopeniaTransmission

Identifiers

PMID31866157
PMCPMC6995686
OpenAlexW2987737829

What OpenQuestion holds

Textmetadata
LicenceTDM
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.