Evidence map›Paper›PMID 31789291›Full record

ArticleJournal of musculoskeletal & neuronal interactions2019

Comparing effects of rest with or without a NK1RA on fibrosis and sensorimotor declines induced by a voluntary moderate demand task.

Mary F Barbe, Amanda R White, Brendan A Hilliard, Danielle M Salvadeo, Mamta Amin, Michele Y Harris, Geneva E Cruz, Lucas Hobson, Steven N Popoff

Abstract read
In one paragraph

Article in Journal of musculoskeletal & neuronal interactions, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Blocking CTGF/CCN2 reduces established skeletal muscle fibrosis in a rat model of overuse injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    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

9 authors.

Mary F BarbeAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Amanda R WhiteAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Brendan A HilliardAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Danielle M SalvadeoAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Mamta AminAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Michele Y HarrisAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Geneva E CruzAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Lucas HobsonAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.
Steven N PopoffAnatomy and Cell Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, USA.

Funding

Biomarkers of Tissue Tolerance and Behavior in a Rat ModelR01AR056019 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI BARBE, MARY F · 2009 to 2025
$7.3M
NIAMS NIH HHS R01 AR056019
6 · The paper itself

Abstract

objectivesFibrosis is one contributing factor in motor dysfunction and discomfort in patients with overuse musculoskeletal disorders. We pharmacologically targeted the primary receptor for Substance P, neurokinin-1, using a specific antagonist (NK1RA) in a rat model of overuse with the goal of improving tissue fibrosis and discomfort.

methodsFemale rats performed a low repetition, high force (LRHF) grasping task for 12 weeks, or performed the task for 12 weeks before being placed on a four week rest break, with or without simultaneous NK1RA treatment. Results were compared to control rats (untreated, or treated 4 weeks with NK1RA or vehicle).

resultsRest improved LRHF-induced declines in grip strength, although rest plus NK1RA treatment (Rest/NK1RA) rescued it. Both treatments improved LRHF-induced increases in muscle TGFβ1 and collagen type 1 levels, forepaw mechanical hypersensitivity (Rest/NK1RA more effectively), macrophage influx into median nerves, and enhanced collagen deposition in forepaw dermis. Only Rest/NK1RA reduced muscle hypercellularity. However, LRHF+4wk Rest /NK1RA rats showed hyposensitivity to noxious hot temperatures.

conclusionsWhile the NK1RA induced hot temperature hyposensitivity should be taken into consideration if this or related drug were used long-term, the NK1RA more effectively reduced muscle hypercellularity and improved grip strength and forepaw mechanical hypersensitivity.

Indexed as

AnimalsCytokinesFemaleFibrosisHand StrengthMuscle, SkeletalMuscle StrengthNeurokinin-1 Receptor AntagonistsPsychomotor PerformanceRatsRats, Sprague-DawleyCytokinesNeurokinin-1 Receptor AntagonistsCollagenCummulative Trauma DisordersMuscleNerveTGFbeta 1

Identifiers

PMID31789291
PMCPMC6944794

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.