Evidence map›Paper›PMID 27861125›Full record

ArticleEMBO molecular medicine2016

4-Aminopyridine promotes functional recovery and remyelination in acute peripheral nerve injury.

Kuang-Ching Tseng, Haiyan Li, Andrew Clark, Leigh Sundem, Michael Zuscik, Mark Noble, John Elfar

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
  2. Review
  3. Advancing Peripheral Nerve Regeneration (Nerve SPACE 2025).Journal of hand surgery global online · 2026
    Article
  4. A review of new developments in peripheral nerve regeneration.Biochemistry and biophysics reports · 2026
    Review
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  19. Peripheral Nerve Injury Treatments and Advances: One Health Perspective.International journal of molecular sciences · 2022
    Review
  20. 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

7 authors at 1 institution in 1 country.

Kuang-Ching TsengCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, USA.
Haiyan LiCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, USA.
Andrew ClarkDepartment of Orthopaedics & Rehabilitation, University of Rochester Medical Center, Rochester, NY, USA.
Leigh SundemDepartment of Orthopaedics & Rehabilitation, University of Rochester Medical Center, Rochester, NY, USA.
Michael ZuscikCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, USA.
Mark NobleDepartment of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY, USA mark_noble@urmc.rochester.edu openelfar@gmail.com.ORCID 0000-0002-2375-7773
John ElfarCenter for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY, USA mark_noble@urmc.rochester.edu openelfar@gmail.com.
University of Rochester Medical Center · US

Funding

Erythropoietin for NeuroregenerationK08AR060164 · NIAMS · UNIVERSITY OF ROCHESTER · PI ELFAR, JOHN · 2013 to 2017
$578k
NIAMS NIH HHS K08 AR060164
6 · The paper itself

Abstract

Traumatic peripheral nerve damage is a major medical problem without effective treatment options. In repurposing studies on 4-aminopyridine (4-AP), a potassium channel blocker that provides symptomatic relief in some chronic neurological afflictions, we discovered this agent offers significant promise as a small molecule regenerative agent for acute traumatic nerve injury. We found, in a mouse model of sciatic crush injury, that sustained early 4-AP administration increased the speed and extent of behavioral recovery too rapidly to be explained by axonal regeneration. Further studies demonstrated that 4-AP also enhanced recovery of nerve conduction velocity, promoted remyelination, and increased axonal area post-injury. We additionally found that 4-AP treatment enables distinction between incomplete and complete lesions more rapidly than existing approaches, thereby potentially addressing the critical challenge of more effectively distinguishing injured individuals who may require mutually exclusive treatment approaches. Thus, 4-AP singularly provides both a new potential therapy to promote durable recovery and remyelination in acute peripheral nerve injury and a means of identifying lesions in which this therapy would be most likely to be of value.

Indexed as

4-AminopyridineAnimalsDisease Models, AnimalMiceNeural ConductionNeuroprotective AgentsPeripheral Nerve InjuriesPotassium Channel BlockersSciatic NeuropathyTreatment Outcome4-AminopyridineNeuroprotective AgentsPotassium Channel Blockers4‐aminopyridinelocalized deliverynerve conduction velocityperipheral nerve injuryremyelination

Identifiers

PMID27861125
PMCPMC5167128
OpenAlexW2549310065

What OpenQuestion holds

Textmetadata
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.