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The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap
Investigating the effect of four types of artificial nerve graft (ANG) structures on rat sciatic nerve defect repair will aid future ANG designs. In this study, fibroin fibers and polylactic acid were used to prepare four ANGs with differing structures: nerve conduit with micron‐sized pores (Conduit...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659138/ https://www.ncbi.nlm.nih.gov/pubmed/28782192 http://dx.doi.org/10.1002/jbm.a.36172 |
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author | Zhou, Chan Liu, Bin Huang, Yong Zeng, Xiu You, Huajian Li, Jin Zhang, Yaoguang |
author_facet | Zhou, Chan Liu, Bin Huang, Yong Zeng, Xiu You, Huajian Li, Jin Zhang, Yaoguang |
author_sort | Zhou, Chan |
collection | PubMed |
description | Investigating the effect of four types of artificial nerve graft (ANG) structures on rat sciatic nerve defect repair will aid future ANG designs. In this study, fibroin fibers and polylactic acid were used to prepare four ANGs with differing structures: nerve conduit with micron‐sized pores (Conduit with pore group), nerve conduit without micron‐sized pores (Conduit group), nerve scaffold comprising Conduit with pore group material plus silk fibers (Scaffold with pore group), and nerve scaffold comprising Conduit group material plus silk fibers (Scaffold group). ANGs or autologous nerves (Autologous group) were implanted into 10 mm rat sciatic nerve defects (n = 50 per group). Twenty weeks after nerve grafting, the time required to retract the surgical limb from the hot water was ranked as follows: Conduit with pore group > Scaffold with pore group > Conduit group > Scaffold group > Autologous group. The static sciatic index was ranked in descending order: Autologous group > Scaffold group > Conduit group > Scaffold with pore group > Conduit with pore group. Immunofluorescence staining identified significant differences in the distribution and number of axons, Schwann cells, and fibroblasts. These findings indicate that ANGs with micron‐sized pores had a negative impact on the repair of peripheral nerve defects, while internal microchannels were beneficial. © 2017 The Authors. Journal of Biomedical Materials Research Part A Published by Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 3077–3085, 2017. |
format | Online Article Text |
id | pubmed-5659138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56591382017-11-03 The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap Zhou, Chan Liu, Bin Huang, Yong Zeng, Xiu You, Huajian Li, Jin Zhang, Yaoguang J Biomed Mater Res A Original Articles Investigating the effect of four types of artificial nerve graft (ANG) structures on rat sciatic nerve defect repair will aid future ANG designs. In this study, fibroin fibers and polylactic acid were used to prepare four ANGs with differing structures: nerve conduit with micron‐sized pores (Conduit with pore group), nerve conduit without micron‐sized pores (Conduit group), nerve scaffold comprising Conduit with pore group material plus silk fibers (Scaffold with pore group), and nerve scaffold comprising Conduit group material plus silk fibers (Scaffold group). ANGs or autologous nerves (Autologous group) were implanted into 10 mm rat sciatic nerve defects (n = 50 per group). Twenty weeks after nerve grafting, the time required to retract the surgical limb from the hot water was ranked as follows: Conduit with pore group > Scaffold with pore group > Conduit group > Scaffold group > Autologous group. The static sciatic index was ranked in descending order: Autologous group > Scaffold group > Conduit group > Scaffold with pore group > Conduit with pore group. Immunofluorescence staining identified significant differences in the distribution and number of axons, Schwann cells, and fibroblasts. These findings indicate that ANGs with micron‐sized pores had a negative impact on the repair of peripheral nerve defects, while internal microchannels were beneficial. © 2017 The Authors. Journal of Biomedical Materials Research Part A Published by Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 3077–3085, 2017. John Wiley and Sons Inc. 2017-08-21 2017-11 /pmc/articles/PMC5659138/ /pubmed/28782192 http://dx.doi.org/10.1002/jbm.a.36172 Text en © 2017 The Authors. The Authors. Journal of Biomedical Materials Research Part A Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Zhou, Chan Liu, Bin Huang, Yong Zeng, Xiu You, Huajian Li, Jin Zhang, Yaoguang The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title | The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title_full | The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title_fullStr | The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title_full_unstemmed | The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title_short | The effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
title_sort | effect of four types of artificial nerve graft structures on the repair of 10‐mm rat sciatic nerve gap |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659138/ https://www.ncbi.nlm.nih.gov/pubmed/28782192 http://dx.doi.org/10.1002/jbm.a.36172 |
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