Evidence map›Paper›PMID 30660008›Full record

ArticleActa biomaterialia2019

Laminin polymer treatment accelerates repair of the crushed peripheral nerve in adult rats.

Agnes E Haggerty, Maria R Bening, Gordon Pherribo, Edward A Dauer, Martin Oudega

Abstract read
In one paragraph

Article in Acta biomaterialia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Bio-Scaffolds as Cell or Exosome Carriers for Nerve Injury Repair.International journal of molecular sciences · 2021
    Review
  6. Review
  7. Article
  8. 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 3 institutions in 2 countries.

Agnes E HaggertyThe Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, FL, USA. Electronic address: aeh92@med.miami.edu.
Maria R BeningDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA, USA.
Gordon PherriboDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA, USA.
Edward A DauerDepartment of Biomedical Engineering, University of Miami, Miami, FL, USA.
Martin OudegaThe Miami Project to Cure Paralysis, University of Miami Miller School of Medicine, Miami, FL, USA; Department of Neurological Surgery, University of Miami Miller School of Medicine, Miami, FL, USA; Bruce W. Carter Department of Veterans Affairs Medical Center, Miami, FL, USA; Affiliated Cancer Hospital & Institute, Guangzhou Medical University, Guangzhou, China. Electronic address: moudega@miami.edu.
University of Miami · USCarnegie Mellon University · USUniversity of Pittsburgh · US

Funding

Mechanisms of 6-AN facilitated Schwann cell-astrocyte interminglingR21NS101298 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI OUDEGA, MARTIN · 2018 to 2019
$422k
NINDS NIH HHS R21 NS101298RRD VA I01 RX001807
6 · The paper itself

Abstract

Promoting axon growth after peripheral nerve injury may support recovery. Soluble laminin polymers formed at pH 4 (aLam) accelerate axon growth from adult dorsal root ganglion neurons in vitro. We used an adult rat model of a peripheral (peroneal) nerve crush to investigate whether an injection of aLam enhances axon growth and functional recovery in vivo. Rats that received an injection of aLam into the crush at 2 days post-injury show significant improvements in hind limb motor function at 2 and 5 weeks after injury compared with control rats that received phosphate-buffered saline. Functional improvement was not associated with changes in sensitivity to thermal or mechanical stimuli. Treatment with aLam decreased the occurrence of autophagia and abolished non-compliance with treadmill walking. Rats treated with aLam showed increased axon presence in the crush site at 2 weeks post-injury and larger axon diameter at 10 weeks post-injury compared with controls. Treatment with aLam did not affect Schwann cell presence or axon myelination. Our results demonstrated that aLam accelerates axon growth and maturity in a crushed peroneal nerve associated with expedited hind limb motor function recovery. Our data support the therapeutic potential of injectable aLam polymers for treatment of peripheral nerve crush injuries. STATEMENT OF SIGNIFICANCE: Incidence of peripheral nerve injury has been estimated to be as high as 5% of all cases entering a Level 1 trauma center and the majority of cases are young males. Peripheral nerves have some endogenous repair capabilities, but overall recovery of function remains limited, which typically has devastating effects on the individual, family, and society, as wages are lost and rehabilitation is extended until the nerves can repair. We report here that laminin polymers injected into a crush accelerated repair and recovery, had no adverse effects on sensory function, obliterated non-compliance for walking tests, and decreased the occurrence of autophagia. These data support the use of laminin polymers for safe and effective recovery after peripheral nerve injury.

Indexed as

Nerve CrushAnimalsAxonsCrush InjuriesFemaleHydrogen-Ion ConcentrationLamininMotor ActivityMyelin SheathNerve RegenerationPeripheral Nerve InjuriesPeroneal NervePhysical Conditioning, AnimalPolymersRats, Sprague-DawleySchwann CellsLamininPolymersAutophagiaAxon regenerationBiomaterialExtracellular matrixLamininNerve repairPeroneal functional index

Identifiers

PMID30660008
PMCPMC6444353
OpenAlexW2910746761

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.