Evidence map›Paper›PMID 22001505›Full record

ArticleInjury2012

An in vivo rodent model of contraction-induced injury in the quadriceps muscle.

Stephen J P Pratt, Michael W Lawlor, Sameer B Shah, Richard M Lovering

Abstract read
In one paragraph

Article in Injury, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. ACS chemical neuroscience · 2021
    Article
  6. Article
  7. Article
  8. Glycerol induces early fibrosis in regenerating rat skeletal muscle.The Journal of veterinary medical science · 2018
    Article
  9. Article
  10. Review
  11. A method to test contractility of the supraspinatus muscle in mouse, rat, and rabbit.Journal of applied physiology (Bethesda, Md. : 1985) · 2016
    Article
  12. In Vivo Assessment of Muscle Contractility in Animal Studies.Methods in molecular biology (Clifton, N.J.) · 2016
    Article
  13. SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models.American journal of physiology. Cell physiology · 2015
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

4 authors at 3 institutions in 1 country.

Stephen J P PrattUniversity of Maryland School of Medicine, Department of Orthopaedics, Baltimore, MD, United States.
Michael W Lawlor
Sameer B Shah
Richard M Lovering
University of Maryland, Baltimore · USBoston Children's Hospital · USUniversity of Maryland, College Park · US

Funding

Progenitor Cells inHuman Skeletal MuscleP50NS040828 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI KUNKEL, LOUIS M · 2008 to 2011
$5.9M
Mechanisms of Force Loss in Injured and Dystrophic Skeletal MuscleR01AR059179 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI LOVERING, RICHARD M · 2010 to 2014
$1.4M
The Role of Intermediate Filaments in Skeletal Muscle Injury and DiseaseK01AR053235 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI LOVERING, RICHARD M · 2007 to 2011
$654k
Mechanisms and efficacy of myostatin inhibition in myotubular myopathyK08AR059750 · NIAMS · MEDICAL COLLEGE OF WISCONSIN · PI LAWLOR, MICHAEL WILLIAM · 2010 to 2014
$641k
NIAMS NIH HHS 1R01AR059179NIAMS NIH HHS K01 AR053235NIAMS NIH HHS K01AR053235NIAMS NIH HHS K08 AR059750NIAMS NIH HHS L40 AR057721NIAMS NIH HHS R01 AR059179NINDS NIH HHS P50 NS040828
6 · The paper itself

Abstract

Most animal studies of muscle contractile function utilise the anterior or posterior crural muscle (dorsiflexors and plantarflexors, respectively). An advantage to using these muscles is that the common fibular and tibial nerves are readily accessible, while the small size of the crural muscles is a disadvantage. Working with small muscles not only makes some in vivo imaging and the muscle testing techniques more challenging, but also provides limited amounts of tissue to study. The purpose of this study was to describe a new animal muscle injury model in the quadriceps that results in a significant and reproducible loss of force. The thigh of Sprague Dawley rats (N=5) and C57BL/10 mice (N=5) was immobilised and the ankle was attached to a custom-made lever arm. The femoral nerve was stimulated using subcutaneous electrodes and injury was induced using 50 lengthening ("eccentric") contractions through a 70° arc of knee motion. This protocol produces a significant and reproducible injury, with comparable susceptibility to injury in the rats and mice. This novel model shows that the quadriceps muscle provides a means to study whole muscle contractility, injury, and recovery in vivo. In addition to the usual benefits of an in vivo model, the larger size of the quadriceps facilitates in vivo imaging and provides a significant increase in the amount of tissue available for histology and biochemistry studies. A controlled muscle injury in the quadriceps also allows one to study a muscle, with mixed fibre types, which is extremely relevant to gait in humans and quadruped models.

Indexed as

Disease Models, AnimalMuscle ContractionAnimalsBiomechanical PhenomenaHindlimbMaleMiceMice, Inbred C57BLQuadriceps MuscleRatsRats, Sprague-Dawley

Identifiers

PMID22001505
PMCPMC3310278
OpenAlexW2069963937

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.