PEG-fusion of viable sciatic nerve isografts restores axonal structure and behavioral recovery after segmental-loss sciatic nerve injuries in Lewis rats

Segmental-loss peripheral nerve injuries (SL-PNIs) often produce severe deficits in sensory/motor functions and voluntary behaviors. The current gold standard for repair is neurorrhaphy of a cable autograft that (1) produces donor site morbidity; (2) results in rapid Wallerian degeneration (WD) of severed distal nerve segments; (3) relies on slow (1-2 mm/day) axonal regeneration; (4) does not prevent atrophy of denervated muscles and sensory structures; and (5) results in poor to non-existent recovery of sensory/motor functions and voluntary behaviors, especially with longer segmental-loss gaps and/or with denervated targets located rather distal to a proximal SL-PNI. Our study used genetically identical Lewis rats as a model system for isograft transplants. Neurorrhaphy of viable peripheral nerve isografts (VPNIs) of 5- or 10-mm length was performed to repair sciatic SL-PNIs of 4- or 8-mm gap length, respectively. Animals were repaired with a set of well-specified solutions that did (PEG-fusion group) or did not (Negative Control [NC] group) contain 50% w/w 3.35 kDa polyethylene glycol (PEG), an axolemmal fusogen at that specific weight and concentration. We also examined the effects of locally applied FK506 on 10-mm VPNI repairs both with and without PEG-fusion. We hypothesized that PEG-fusion groups would show better axonal morphology and behavioral recovery, as assessed by the Sciatic Functional Index (SFI), compared to NC groups regardless of the gap length. We also hypothesized that FK506 would improve the effects of PEG-fusion by reducing inflammation. Our data showed that PEG-fused VPNI groups had significantly larger axonal diameters and lower g-ratios, less WD, and better SFI scores compared to NC groups regardless of the gap lengths for SL-PNIs. However, localized FK506 treatment only transiently improved axonal regeneration and impaired long-term SFI behavioral recovery, which is the most important measure of successful repairs. In conclusion, PEG-fusion repair technologies show great potential for improving clinical treatments.

Authors

Institutions

Publication Details

Journal
PLoS ONE
Published
2026-05-21
DOI
https://doi.org/10.1371/journal.pone.0349204
Primary Topic
Nerve injury and regeneration
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

PEG-fusion of viable sciatic nerve isografts restores axonal structure and behavioral recovery after segmental-loss sciatic nerve injuries in Lewis rats

Arjun Agarwal, George D. Bittner, Joseph F. Alderete, Guhan Periyasamy et al.
PLoS ONE
Nerve injury and regeneration
article

PEG-fusion of viable sciatic nerve isografts restores axonal structure and behavioral recovery after segmental-loss sciatic nerve injuries in Lewis rats

Arjun Agarwal, George D. Bittner, Joseph F. Alderete, Guhan Periyasamy, Cathy Z. Yang, Liwen Zhou, Alexa Olivarez, Varun Gokhale, Henry A. Garcia, Rhea Sood, Alexander M. Schafer
article en

Abstract

Segmental-loss peripheral nerve injuries (SL-PNIs) often produce severe deficits in sensory/motor functions and voluntary behaviors. The current gold standard for repair is neurorrhaphy of a cable autograft that (1) produces donor site morbidity; (2) results in rapid Wallerian degeneration (WD) of severed distal nerve segments; (3) relies on slow (1-2 mm/day) axonal regeneration; (4) does not prevent atrophy of denervated muscles and sensory structures; and (5) results in poor to non-existent recovery of sensory/motor functions and voluntary behaviors, especially with longer segmental-loss gaps and/or with denervated targets located rather distal to a proximal SL-PNI. Our study used genetically identical Lewis rats as a model system for isograft transplants. Neurorrhaphy of viable peripheral nerve isografts (VPNIs) of 5- or 10-mm length was performed to repair sciatic SL-PNIs of 4- or 8-mm gap length, respectively. Animals were repaired with a set of well-specified solutions that did (PEG-fusion group) or did not (Negative Control [NC] group) contain 50% w/w 3.35 kDa polyethylene glycol (PEG), an axolemmal fusogen at that specific weight and concentration. We also examined the effects of locally applied FK506 on 10-mm VPNI repairs both with and without PEG-fusion. We hypothesized that PEG-fusion groups would show better axonal morphology and behavioral recovery, as assessed by the Sciatic Functional Index (SFI), compared to NC groups regardless of the gap length. We also hypothesized that FK506 would improve the effects of PEG-fusion by reducing inflammation. Our data showed that PEG-fused VPNI groups had significantly larger axonal diameters and lower g-ratios, less WD, and better SFI scores compared to NC groups regardless of the gap lengths for SL-PNIs. However, localized FK506 treatment only transiently improved axonal regeneration and impaired long-term SFI behavioral recovery, which is the most important measure of successful repairs. In conclusion, PEG-fusion repair technologies show great potential for improving clinical treatments.

PLoS ONEVol. 21(5)
The University of Texas at San Antonio Health Science Center (US), The University of Texas at Austin (US)
U.S. Department of Defense
No poverty
Openalex Percentile: Top 8%
Nerve injury and regeneration
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.