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Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats
Treatment of peripheral nerve injuries (PNIs) remains a challenge. Interposing a graft delivers better regenerative outcomes. Autografts present major drawbacks which have given rise to the development of alternatives such as artificial scaffolds, some of which are very promising. This study was des...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675695/ https://www.ncbi.nlm.nih.gov/pubmed/35503142 http://dx.doi.org/10.1007/s10561-022-10006-8 |
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author | Lecoq, Flore-Anne Barnouin, Laurence Ardouin, Ludovic Hartmann, Daniel Obert, Laurent |
author_facet | Lecoq, Flore-Anne Barnouin, Laurence Ardouin, Ludovic Hartmann, Daniel Obert, Laurent |
author_sort | Lecoq, Flore-Anne |
collection | PubMed |
description | Treatment of peripheral nerve injuries (PNIs) remains a challenge. Interposing a graft delivers better regenerative outcomes. Autografts present major drawbacks which have given rise to the development of alternatives such as artificial scaffolds, some of which are very promising. This study was designed to investigate the potential use of an inverted human umbilical cord artery (iHUA) as a 3D scaffold nerve chamber, for nerve regeneration after transection of the sciatic nerve (SN) in rats. Rats underwent surgical SN transection in their right hindlimb, followed by suture of the device at the resected stumps. Local tolerance, insert biodegradability and nerve reconstruction over time were thoroughly studied by histopathological and morphometric analysis, completed by functional test assessment of sensitivity and motricity recovery. We have demonstrated that nerve reconstruction in the presence of an iHUA insert is effective. The device is well tolerated and highly biodegraded. Although the regenerated nerve is still immature at the end of our study, signs of sensitivity and partial functional recovery were witnessed, confirming our histological findings. Our results support the potential clinical use of iHUA as a 3D scaffold to bridge nerve discontinuity and guide axonal regrowth in selected cases of PNIs. |
format | Online Article Text |
id | pubmed-9675695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-96756952022-11-21 Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats Lecoq, Flore-Anne Barnouin, Laurence Ardouin, Ludovic Hartmann, Daniel Obert, Laurent Cell Tissue Bank Full Length Paper Treatment of peripheral nerve injuries (PNIs) remains a challenge. Interposing a graft delivers better regenerative outcomes. Autografts present major drawbacks which have given rise to the development of alternatives such as artificial scaffolds, some of which are very promising. This study was designed to investigate the potential use of an inverted human umbilical cord artery (iHUA) as a 3D scaffold nerve chamber, for nerve regeneration after transection of the sciatic nerve (SN) in rats. Rats underwent surgical SN transection in their right hindlimb, followed by suture of the device at the resected stumps. Local tolerance, insert biodegradability and nerve reconstruction over time were thoroughly studied by histopathological and morphometric analysis, completed by functional test assessment of sensitivity and motricity recovery. We have demonstrated that nerve reconstruction in the presence of an iHUA insert is effective. The device is well tolerated and highly biodegraded. Although the regenerated nerve is still immature at the end of our study, signs of sensitivity and partial functional recovery were witnessed, confirming our histological findings. Our results support the potential clinical use of iHUA as a 3D scaffold to bridge nerve discontinuity and guide axonal regrowth in selected cases of PNIs. Springer Netherlands 2022-05-03 2022 /pmc/articles/PMC9675695/ /pubmed/35503142 http://dx.doi.org/10.1007/s10561-022-10006-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Full Length Paper Lecoq, Flore-Anne Barnouin, Laurence Ardouin, Ludovic Hartmann, Daniel Obert, Laurent Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title | Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title_full | Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title_fullStr | Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title_full_unstemmed | Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title_short | Inverted human umbilical artery as a 3D scaffold for sciatic nerve regeneration in rats |
title_sort | inverted human umbilical artery as a 3d scaffold for sciatic nerve regeneration in rats |
topic | Full Length Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675695/ https://www.ncbi.nlm.nih.gov/pubmed/35503142 http://dx.doi.org/10.1007/s10561-022-10006-8 |
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