Surgical Angiogenesis of Decellularized Nerve Allografts Improves Early Functional Recovery in a Rat Sciatic Nerve Defect Model.


Journal

Plastic and reconstructive surgery
ISSN: 1529-4242
Titre abrégé: Plast Reconstr Surg
Pays: United States
ID NLM: 1306050

Informations de publication

Date de publication:
01 Sep 2021
Historique:
pubmed: 23 7 2021
medline: 13 1 2022
entrez: 22 7 2021
Statut: ppublish

Résumé

Surgical angiogenesis applied to nerve grafts has been suggested to enhance nerve regeneration after nerve injury. The authors hypothesized that surgical angiogenesis to decellularized nerve allografts would improve functional recovery in a rat sciatic nerve defect model. Sixty Lewis rats were divided in three groups of 20 animals each. Unilateral sciatic nerve defects were repaired with (1) autografts, (2) decellularized allografts, and (3) decellularized allografts wrapped with a superficial inferior epigastric artery fascial flap to add surgical angiogenesis. Twelve and 16 weeks after surgery, nerve regeneration was assessed using functional, electrophysiologic, histologic, and immunofluorescence analyses. Ultrasonography was used during the survival period to noninvasively evaluate muscle atrophy and reinnervation by measuring cross-sectional muscle area. Surgical angiogenesis of allografts demonstrated significantly improved isometric tetanic force recovery at 12 weeks, compared to allograft alone, which normalized between groups at 16 weeks. Cross-sectional muscle areas showed no differences between groups. Electrophysiology showed superiority of autografts at both time points. No differences were found in histologic analysis, besides a significantly inferior N ratio in allografts at 12 weeks. Immunofluorescent expression of CD34, indicating vascularity, was significantly enhanced in the superficial inferior epigastric artery fascial group compared to allografts at 12 weeks, with highest expression at 16 weeks compared to all groups. Surgical angiogenesis with an adipofascial flap to the nerve allograft increases vascularity in the nerve graft, with subsequent improvement of early muscle force recovery, comparable to autografts.

Sections du résumé

BACKGROUND BACKGROUND
Surgical angiogenesis applied to nerve grafts has been suggested to enhance nerve regeneration after nerve injury. The authors hypothesized that surgical angiogenesis to decellularized nerve allografts would improve functional recovery in a rat sciatic nerve defect model.
METHODS METHODS
Sixty Lewis rats were divided in three groups of 20 animals each. Unilateral sciatic nerve defects were repaired with (1) autografts, (2) decellularized allografts, and (3) decellularized allografts wrapped with a superficial inferior epigastric artery fascial flap to add surgical angiogenesis. Twelve and 16 weeks after surgery, nerve regeneration was assessed using functional, electrophysiologic, histologic, and immunofluorescence analyses. Ultrasonography was used during the survival period to noninvasively evaluate muscle atrophy and reinnervation by measuring cross-sectional muscle area.
RESULTS RESULTS
Surgical angiogenesis of allografts demonstrated significantly improved isometric tetanic force recovery at 12 weeks, compared to allograft alone, which normalized between groups at 16 weeks. Cross-sectional muscle areas showed no differences between groups. Electrophysiology showed superiority of autografts at both time points. No differences were found in histologic analysis, besides a significantly inferior N ratio in allografts at 12 weeks. Immunofluorescent expression of CD34, indicating vascularity, was significantly enhanced in the superficial inferior epigastric artery fascial group compared to allografts at 12 weeks, with highest expression at 16 weeks compared to all groups.
CONCLUSION CONCLUSIONS
Surgical angiogenesis with an adipofascial flap to the nerve allograft increases vascularity in the nerve graft, with subsequent improvement of early muscle force recovery, comparable to autografts.

Identifiants

pubmed: 34292916
doi: 10.1097/PRS.0000000000008291
pii: 00006534-202109000-00012
pmc: PMC8805151
mid: NIHMS1772176
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

561-570

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS102360
Pays : United States

Informations de copyright

Copyright © 2021 by the American Society of Plastic Surgeons.

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Auteurs

Tiam M Saffari (TM)

From the Department of Orthopedic Surgery, Mayo Clinic; and the Department of Plastic, Reconstructive, and Hand Surgery, Radboud University.

Femke Mathot (F)

From the Department of Orthopedic Surgery, Mayo Clinic; and the Department of Plastic, Reconstructive, and Hand Surgery, Radboud University.

Patricia F Friedrich (PF)

From the Department of Orthopedic Surgery, Mayo Clinic; and the Department of Plastic, Reconstructive, and Hand Surgery, Radboud University.

Allen T Bishop (AT)

From the Department of Orthopedic Surgery, Mayo Clinic; and the Department of Plastic, Reconstructive, and Hand Surgery, Radboud University.

Alexander Y Shin (AY)

From the Department of Orthopedic Surgery, Mayo Clinic; and the Department of Plastic, Reconstructive, and Hand Surgery, Radboud University.

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