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Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis

Electrical stimulation has been shown to accelerate and enhance nerve regeneration in sensory and motor neurons after injury, but there is little evidence that focuses on the varying degrees of fibrosis in the delayed repair of peripheral nerve tissue. In this study, a rat model of sciatic nerve tra...

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Autores principales: Han, Na, Xu, Chun-gui, Wang, Tian-bing, Kou, Yu-hui, Yin, Xiao-feng, Zhang, Pei-xun, Xue, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357124/
https://www.ncbi.nlm.nih.gov/pubmed/25788926
http://dx.doi.org/10.4103/1673-5374.150714
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author Han, Na
Xu, Chun-gui
Wang, Tian-bing
Kou, Yu-hui
Yin, Xiao-feng
Zhang, Pei-xun
Xue, Feng
author_facet Han, Na
Xu, Chun-gui
Wang, Tian-bing
Kou, Yu-hui
Yin, Xiao-feng
Zhang, Pei-xun
Xue, Feng
author_sort Han, Na
collection PubMed
description Electrical stimulation has been shown to accelerate and enhance nerve regeneration in sensory and motor neurons after injury, but there is little evidence that focuses on the varying degrees of fibrosis in the delayed repair of peripheral nerve tissue. In this study, a rat model of sciatic nerve transection injury was repaired with a biodegradable conduit at 1 day, 1 week, 1 month and 2 months after injury, when the rats were divided into two subgroups. In the experimental group, rats were treated with electrical stimuli of frequency of 20 Hz, pulse width 100 ms and direct current voltage of 3 V; while rats in the control group received no electrical stimulation after the conduit operation. Histological results showed that stained collagen fibers comprised less than 20% of the total operated area in the two groups after delayed repair at both 1 day and 1 week but after longer delays, the collagen fiber area increased with the time after injury. Immunohistochemical staining revealed that the expression level of transforming growth factor β (an indicator of tissue fibrosis) decreased at both 1 day and 1 week after delayed repair but increased at both 1 and 2 months after delayed repair. These findings indicate that if the biodegradable conduit repair combined with electrical stimulation is delayed, it results in a poor outcome following sciatic nerve injury. One month after injury, tissue degeneration and distal fibrosis are apparent and are probably the main reason why electrical stimulation fails to promote nerve regeneration after delayed repair.
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spelling pubmed-43571242015-03-18 Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis Han, Na Xu, Chun-gui Wang, Tian-bing Kou, Yu-hui Yin, Xiao-feng Zhang, Pei-xun Xue, Feng Neural Regen Res Special Issue Electrical stimulation has been shown to accelerate and enhance nerve regeneration in sensory and motor neurons after injury, but there is little evidence that focuses on the varying degrees of fibrosis in the delayed repair of peripheral nerve tissue. In this study, a rat model of sciatic nerve transection injury was repaired with a biodegradable conduit at 1 day, 1 week, 1 month and 2 months after injury, when the rats were divided into two subgroups. In the experimental group, rats were treated with electrical stimuli of frequency of 20 Hz, pulse width 100 ms and direct current voltage of 3 V; while rats in the control group received no electrical stimulation after the conduit operation. Histological results showed that stained collagen fibers comprised less than 20% of the total operated area in the two groups after delayed repair at both 1 day and 1 week but after longer delays, the collagen fiber area increased with the time after injury. Immunohistochemical staining revealed that the expression level of transforming growth factor β (an indicator of tissue fibrosis) decreased at both 1 day and 1 week after delayed repair but increased at both 1 and 2 months after delayed repair. These findings indicate that if the biodegradable conduit repair combined with electrical stimulation is delayed, it results in a poor outcome following sciatic nerve injury. One month after injury, tissue degeneration and distal fibrosis are apparent and are probably the main reason why electrical stimulation fails to promote nerve regeneration after delayed repair. Medknow Publications & Media Pvt Ltd 2015-01 /pmc/articles/PMC4357124/ /pubmed/25788926 http://dx.doi.org/10.4103/1673-5374.150714 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue
Han, Na
Xu, Chun-gui
Wang, Tian-bing
Kou, Yu-hui
Yin, Xiao-feng
Zhang, Pei-xun
Xue, Feng
Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title_full Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title_fullStr Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title_full_unstemmed Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title_short Electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
title_sort electrical stimulation does not enhance nerve regeneration if delayed after sciatic nerve injury: the role of fibrosis
topic Special Issue
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357124/
https://www.ncbi.nlm.nih.gov/pubmed/25788926
http://dx.doi.org/10.4103/1673-5374.150714
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