Evidence map›Paper›PMID 29659058›Full record

ArticleJournal of neuroscience research2018

Polyethylene glycol solutions rapidly restore and maintain axonal continuity, neuromuscular structures, and behaviors lost after sciatic nerve transections in female rats.

Michelle Mikesh, Cameron L Ghergherehchi, Robert Louis Hastings, Amir Ali, Sina Rahesh, Karthik Jagannath, Dale R Sengelaub, Richard C Trevino, David M Jackson, George D Bittner

Erratum issuedAbstract read
In one paragraph

Article in Journal of neuroscience research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–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

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  16. Compound Motor Action Potentials During a Modest Nerve Crush.Frontiers in cellular neuroscience · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Michelle MikeshDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.
Cameron L GhergherehchiInstitute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas.ORCID 0000-0003-2125-1186
Robert Louis HastingsDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.
Amir AliDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.
Sina RaheshDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.
Karthik JagannathDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.
Dale R SengelaubDepartment of Psychological and Brain Sciences, Indiana University, Bloomington, Indiana.
Richard C TrevinoDepartment of Orthopedic Surgery, Wellspan Teaching Hospitals, York, Pennsylvania.
David M JacksonNeuraptive Therapeutics, Lafayette, Colorado.
George D BittnerDepartment of Neuroscience, University of Texas at Austin, Austin, Texas.ORCID 0000-0002-5610-6264

Funding

A novel bioengineered technique to rapidly and permanently repair cut PNS nervesR01NS081063 · NINDS · UNIVERSITY OF TEXAS AT AUSTIN · PI BITTNER, GEORGE DAVIS · 2012 to 2016
$1.7M
NINDS NIH HHS R01 NS081063
6 · The paper itself

Abstract

Complete severance of major peripheral mixed sensory-motor nerve proximally in a mammalian limb produces immediate loss of action potential conduction and voluntary behaviors mediated by the severed distal axonal segments. These severed distal segments undergo Wallerian degeneration within days. Denervated muscles atrophy within weeks. Slowly regenerating (∼1 mm/day) outgrowths from surviving proximal stumps that often nonspecifically reinnervate denervated targets produce poor, if any, restoration of lost voluntary behaviors. In contrast, in this study using completely transected female rat sciatic axons as a model system, we provide extensive morphometric, immunohistochemical, electrophysiological, and behavioral data to show that these adverse outcomes are avoided by microsuturing closely apposed axonal cut ends (neurorrhaphy) and applying a sequence of well-specified solutions, one of which contains polyethylene glycol (PEG). This "PEG-fusion" procedure within minutes reestablishes axoplasmic and axolemmal continuity and signaling by nonspecifically fusing (connecting) closely apposed open ends of severed motor and/or sensory axons at the lesion site. These PEG-fused axons continue to conduct action potentials and generate muscle action potentials and muscle twitches for months and do not undergo Wallerian degeneration. Continuously innervated muscle fibers undergo much less atrophy compared with denervated muscle fibers. Dramatic behavioral recovery to near-unoperated levels occurs within days to weeks, almost certainly by activating many central nervous system and peripheral nervous system synaptic and other plasticities, some perhaps to a greater extent than most neuroscientists would expect. Negative control transections in which neurorrhaphy and all solutions except the PEG-containing solution are applied produce none of these remarkably fortuitous outcomes observed for PEG-fusion.

Indexed as

AnimalsAxonsAxotomyDisease Models, AnimalFemaleNerve RegenerationNeural ConductionNeuromuscular JunctionPolyethylene GlycolsRatsRecovery of FunctionSciatic NerveSciatic NeuropathyWallerian DegenerationPolyethylene Glycolsaxotomynerve regenerationnerve repairpolyethylene glycolsciatic nerveWallerian degeneration

Identifiers

PMID29659058
PMCPMC5980706

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Registered trials

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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.