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End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration
End-to-side neurorrhaphy is an option in the treatment of the long segment defects of a nerve. It involves suturing the distal stump of the disconnected nerve (recipient nerve) to the side of the intimate adjacent nerve (donor nerve). However, the motor-sensory specificity after end-to-side neurorrh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696852/ https://www.ncbi.nlm.nih.gov/pubmed/29171436 http://dx.doi.org/10.4103/1673-5374.217350 |
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author | Yu, Qing Zhang, She-hong Wang, Tao Peng, Feng Han, Dong Gu, Yu-dong |
author_facet | Yu, Qing Zhang, She-hong Wang, Tao Peng, Feng Han, Dong Gu, Yu-dong |
author_sort | Yu, Qing |
collection | PubMed |
description | End-to-side neurorrhaphy is an option in the treatment of the long segment defects of a nerve. It involves suturing the distal stump of the disconnected nerve (recipient nerve) to the side of the intimate adjacent nerve (donor nerve). However, the motor-sensory specificity after end-to-side neurorrhaphy remains unclear. This study sought to evaluate whether cutaneous sensory nerve regeneration induces motor nerves after end-to-side neurorrhaphy. Thirty rats were randomized into three groups: (1) end-to-side neurorrhaphy using the ulnar nerve (mixed sensory and motor) as the donor nerve and the cutaneous antebrachii medialis nerve as the recipient nerve; (2) the sham group: ulnar nerve and cutaneous antebrachii medialis nerve were just exposed; and (3) the transected nerve group: cutaneous antebrachii medialis nerve was transected and the stumps were turned over and tied. At 5 months, acetylcholinesterase staining results showed that 34% ± 16% of the myelinated axons were stained in the end-to-side group, and none of the myelinated axons were stained in either the sham or transected nerve groups. Retrograde fluorescent tracing of spinal motor neurons and dorsal root ganglion showed the proportion of motor neurons from the cutaneous antebrachii medialis nerve of the end-to-side group was 21% ± 5%. In contrast, no motor neurons from the cutaneous antebrachii medialis nerve of the sham group and transected nerve group were found in the spinal cord segment. These results confirmed that motor neuron regeneration occurred after cutaneous nerve end-to-side neurorrhaphy. |
format | Online Article Text |
id | pubmed-5696852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56968522017-12-04 End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration Yu, Qing Zhang, She-hong Wang, Tao Peng, Feng Han, Dong Gu, Yu-dong Neural Regen Res Research Article End-to-side neurorrhaphy is an option in the treatment of the long segment defects of a nerve. It involves suturing the distal stump of the disconnected nerve (recipient nerve) to the side of the intimate adjacent nerve (donor nerve). However, the motor-sensory specificity after end-to-side neurorrhaphy remains unclear. This study sought to evaluate whether cutaneous sensory nerve regeneration induces motor nerves after end-to-side neurorrhaphy. Thirty rats were randomized into three groups: (1) end-to-side neurorrhaphy using the ulnar nerve (mixed sensory and motor) as the donor nerve and the cutaneous antebrachii medialis nerve as the recipient nerve; (2) the sham group: ulnar nerve and cutaneous antebrachii medialis nerve were just exposed; and (3) the transected nerve group: cutaneous antebrachii medialis nerve was transected and the stumps were turned over and tied. At 5 months, acetylcholinesterase staining results showed that 34% ± 16% of the myelinated axons were stained in the end-to-side group, and none of the myelinated axons were stained in either the sham or transected nerve groups. Retrograde fluorescent tracing of spinal motor neurons and dorsal root ganglion showed the proportion of motor neurons from the cutaneous antebrachii medialis nerve of the end-to-side group was 21% ± 5%. In contrast, no motor neurons from the cutaneous antebrachii medialis nerve of the sham group and transected nerve group were found in the spinal cord segment. These results confirmed that motor neuron regeneration occurred after cutaneous nerve end-to-side neurorrhaphy. Medknow Publications & Media Pvt Ltd 2017-10 /pmc/articles/PMC5696852/ /pubmed/29171436 http://dx.doi.org/10.4103/1673-5374.217350 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Yu, Qing Zhang, She-hong Wang, Tao Peng, Feng Han, Dong Gu, Yu-dong End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title | End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title_full | End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title_fullStr | End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title_full_unstemmed | End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title_short | End-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
title_sort | end-to-side neurorrhaphy repairs peripheral nerve injury: sensory nerve induces motor nerve regeneration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696852/ https://www.ncbi.nlm.nih.gov/pubmed/29171436 http://dx.doi.org/10.4103/1673-5374.217350 |
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