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Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed

BACKGROUND: Several types of artificial nerve conduit have been used for bridging peripheral nerve gaps as an alternative to autologous nerves. However, their efficacy in repairing nerve injuries accompanied by surrounding tissue damage remains unclear. We fabricated a novel nerve conduit vasculariz...

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Autores principales: Iijima, Yuki, Ajiki, Takashi, Murayama, Akira, Takeshita, Katsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874309/
https://www.ncbi.nlm.nih.gov/pubmed/27257595
http://dx.doi.org/10.1097/GOX.0000000000000652
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author Iijima, Yuki
Ajiki, Takashi
Murayama, Akira
Takeshita, Katsushi
author_facet Iijima, Yuki
Ajiki, Takashi
Murayama, Akira
Takeshita, Katsushi
author_sort Iijima, Yuki
collection PubMed
description BACKGROUND: Several types of artificial nerve conduit have been used for bridging peripheral nerve gaps as an alternative to autologous nerves. However, their efficacy in repairing nerve injuries accompanied by surrounding tissue damage remains unclear. We fabricated a novel nerve conduit vascularized by superficial inferior epigastric (SIE) vessels and evaluated whether it could promote axonal regeneration in a necrotic bed. METHODS: A 15-mm nerve conduit was implanted beneath the SIE vessels in the groin of a rat to supply it with blood vessels 2 weeks before nerve reconstruction. We removed a 13-mm segment of the sciatic nerve and then pressed a heated iron against the dorsal thigh muscle to produce a burn. The defects were immediately repaired with an autograft (n = 10), nerve conduit graft (n = 8), or vascularized nerve conduit graft (n = 8). Recovery of motor function was examined for 18 weeks after surgery. The regenerated nerves were electrophysiologically and histologically evaluated. RESULTS: The vascularity of the nerve conduit implanted beneath the SIE vessels was confirmed histologically 2 weeks after implantation. Between 14 and 18 weeks after surgery, motor function of the vascularized conduit group was significantly better than that of the nonvascularized conduit group. Electrophysiological and histological evaluations revealed that although the improvement did not reach the level of reinnervation achieved by an autograft, the vascularized nerve conduit improved axonal regeneration more than did the conduit alone. CONCLUSION: Vascularization of artificial nerve conduits accelerated peripheral nerve regeneration, but further research is required to improve the quality of nerve regeneration.
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spelling pubmed-48743092016-06-02 Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed Iijima, Yuki Ajiki, Takashi Murayama, Akira Takeshita, Katsushi Plast Reconstr Surg Glob Open Original Article BACKGROUND: Several types of artificial nerve conduit have been used for bridging peripheral nerve gaps as an alternative to autologous nerves. However, their efficacy in repairing nerve injuries accompanied by surrounding tissue damage remains unclear. We fabricated a novel nerve conduit vascularized by superficial inferior epigastric (SIE) vessels and evaluated whether it could promote axonal regeneration in a necrotic bed. METHODS: A 15-mm nerve conduit was implanted beneath the SIE vessels in the groin of a rat to supply it with blood vessels 2 weeks before nerve reconstruction. We removed a 13-mm segment of the sciatic nerve and then pressed a heated iron against the dorsal thigh muscle to produce a burn. The defects were immediately repaired with an autograft (n = 10), nerve conduit graft (n = 8), or vascularized nerve conduit graft (n = 8). Recovery of motor function was examined for 18 weeks after surgery. The regenerated nerves were electrophysiologically and histologically evaluated. RESULTS: The vascularity of the nerve conduit implanted beneath the SIE vessels was confirmed histologically 2 weeks after implantation. Between 14 and 18 weeks after surgery, motor function of the vascularized conduit group was significantly better than that of the nonvascularized conduit group. Electrophysiological and histological evaluations revealed that although the improvement did not reach the level of reinnervation achieved by an autograft, the vascularized nerve conduit improved axonal regeneration more than did the conduit alone. CONCLUSION: Vascularization of artificial nerve conduits accelerated peripheral nerve regeneration, but further research is required to improve the quality of nerve regeneration. Wolters Kluwer Health 2016-03-22 /pmc/articles/PMC4874309/ /pubmed/27257595 http://dx.doi.org/10.1097/GOX.0000000000000652 Text en Copyright © 2016 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Original Article
Iijima, Yuki
Ajiki, Takashi
Murayama, Akira
Takeshita, Katsushi
Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title_full Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title_fullStr Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title_full_unstemmed Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title_short Effect of Artificial Nerve Conduit Vascularization on Peripheral Nerve in a Necrotic Bed
title_sort effect of artificial nerve conduit vascularization on peripheral nerve in a necrotic bed
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4874309/
https://www.ncbi.nlm.nih.gov/pubmed/27257595
http://dx.doi.org/10.1097/GOX.0000000000000652
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