Evidence map›Paper›PMID 42511670›Full record

ReviewInternational journal of molecular sciences2026

Beneficially Stressing the Peripheral Nervous System to Repair.

Valerie M K Verge, Zhengxin Ying, Wafa A Mustafa, Justin M Naniong, Joelle R Nadeau, Jovan C D Hasmatali, Miles E Magno, Vikram Misra, Gillian D Muir

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Special Issue "Plasticity of the Nervous System After Injury: 2nd Edition".International journal of molecular sciences · 2026
    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.

Valerie M K VergeDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Zhengxin YingDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0003-0948-4948
Wafa A MustafaDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Justin M NaniongDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0000-0002-1094-6778
Joelle R NadeauDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0009-0000-2250-0725
Jovan C D HasmataliDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.
Miles E MagnoDepartment of Anatomy, Physiology and Pharmacology, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.ORCID 0009-0008-2510-4662
Vikram MisraDepartment of Veterinary Microbiology, WCVM, University of Saskatchewan, Saskatoon, SK S7N 5B4, Canada.ORCID 0000-0001-6818-7156
Gillian D MuirCameco MS Neuroscience Research Centre, University of Saskatchewan, Saskatoon, SK S7K 0M7, Canada.ORCID 0000-0002-6426-1651

Funding

CIHR MOP-142328 and PJT-183666
6 · The paper itself

Abstract

Peripheral neurons have an intrinsic capacity for repair, albeit still challenging. How the nervous system responds to the cellular stress imposed by nerve injury and adjunct therapies impacts axon regeneration and functional outcomes. Here, we summarize some of the key primarily axonal and neuronal adaptive stress responses and mechanisms that underlie the ability of peripheral neurons to regenerate an axon. This includes activation of the unfolded protein response and endoplasmic reticulum membrane-associated molecules, namely Luman/CREB3, a transmembrane basic leucine zipper transcription factor that regulates the encoding of beneficial adaptive stress responses that drive the ability of an injured sensory neuron to regenerate their axon. We also highlight an emerging novel non-invasive strategy, therapeutic acute intermittent hypoxia, that imposes a level of beneficial adaptive stress that can alter gene programs induced by the injury to enhance regeneration in a manner akin to the more invasive yet highly effective electrical nerve stimulation. The ability to manipulate and significantly elevate the intrinsic adaptive stress/repair responses of injured peripheral neurons holds therapeutic promise, with accumulating evidence supporting its clinical use.

Indexed as

Nerve RegenerationPeripheral Nerve InjuriesPeripheral Nervous SystemStress, PhysiologicalAnimalsAxonsCyclic AMP Response Element-Binding ProteinHumansUnfolded Protein ResponseCyclic AMP Response Element-Binding Proteinacute intermittent hypoxiaCREB3electrical nerve stimulationendoplasmic reticulum stressLumanmotor neuronmyelinationregenerationsensory neuronunfolded protein response

Identifiers

PMID42511670
PMCPMC13411429

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.