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Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats
Peripheral nerve injuries can cause disabilities, social or economic problems. Melatonin, the secretory product of the pineal gland has antioxidant and anti-inflammatory actions. The aim of the present study was to investigate the effect of melatonin on the recovery of sciatic nerve after injury, co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Leibniz Research Centre for Working Environment and Human Factors
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379119/ https://www.ncbi.nlm.nih.gov/pubmed/28435433 http://dx.doi.org/10.17179/excli2016-763 |
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author | Rateb, Enas Ezzat Amin, Shaimaa Nasr El-Tablawy, Nashwa Rashed, Laila Ahmed El-Attar, Samah |
author_facet | Rateb, Enas Ezzat Amin, Shaimaa Nasr El-Tablawy, Nashwa Rashed, Laila Ahmed El-Attar, Samah |
author_sort | Rateb, Enas Ezzat |
collection | PubMed |
description | Peripheral nerve injuries can cause disabilities, social or economic problems. Melatonin, the secretory product of the pineal gland has antioxidant and anti-inflammatory actions. The aim of the present study was to investigate the effect of melatonin on the recovery of sciatic nerve after injury, comparing its effect when given in the light or the dark periods. Forty adult male Albino rats were allocated into four groups: control, nerve injury, nerve injury + melatonin given at light and nerve injury + melatonin given at dark. Nerve injury was initiated by clamping the sciatic nerve. Sciatic functional index (SFI) was measured preoperatively and postoperatively. Melatonin was given daily for six weeks. Recovery of the function was analyzed by functional analysis, electrophysiological analysis and biochemical measurement of Superoxide dismutase (SOD), Interleukin 1-beta (IL-1 β), Nerve growth factor (NGF), and bcl-2. Melatonin improved SFI, nerve conduction velocity (NCV) and the force of gastrocnemius muscle contraction as compared to the untreated rats. SOD activity, NGF, and bcl-2 were significantly increased, while IL-1β was significantly decreased after melatonin treatment as compared to the untreated injury group. SFI reached the control level; muscle contraction and IL-1B were significantly improved in the group treated with melatonin in the dark. Melatonin fastened the neural recovery and may be used in the treatment of nerve injury and it induced better nerve regeneration when the rats were treated during the dark period. |
format | Online Article Text |
id | pubmed-5379119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
spelling | pubmed-53791192017-04-21 Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats Rateb, Enas Ezzat Amin, Shaimaa Nasr El-Tablawy, Nashwa Rashed, Laila Ahmed El-Attar, Samah EXCLI J Original Article Peripheral nerve injuries can cause disabilities, social or economic problems. Melatonin, the secretory product of the pineal gland has antioxidant and anti-inflammatory actions. The aim of the present study was to investigate the effect of melatonin on the recovery of sciatic nerve after injury, comparing its effect when given in the light or the dark periods. Forty adult male Albino rats were allocated into four groups: control, nerve injury, nerve injury + melatonin given at light and nerve injury + melatonin given at dark. Nerve injury was initiated by clamping the sciatic nerve. Sciatic functional index (SFI) was measured preoperatively and postoperatively. Melatonin was given daily for six weeks. Recovery of the function was analyzed by functional analysis, electrophysiological analysis and biochemical measurement of Superoxide dismutase (SOD), Interleukin 1-beta (IL-1 β), Nerve growth factor (NGF), and bcl-2. Melatonin improved SFI, nerve conduction velocity (NCV) and the force of gastrocnemius muscle contraction as compared to the untreated rats. SOD activity, NGF, and bcl-2 were significantly increased, while IL-1β was significantly decreased after melatonin treatment as compared to the untreated injury group. SFI reached the control level; muscle contraction and IL-1B were significantly improved in the group treated with melatonin in the dark. Melatonin fastened the neural recovery and may be used in the treatment of nerve injury and it induced better nerve regeneration when the rats were treated during the dark period. Leibniz Research Centre for Working Environment and Human Factors 2017-03-06 /pmc/articles/PMC5379119/ /pubmed/28435433 http://dx.doi.org/10.17179/excli2016-763 Text en Copyright © 2017 Rateb et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited. |
spellingShingle | Original Article Rateb, Enas Ezzat Amin, Shaimaa Nasr El-Tablawy, Nashwa Rashed, Laila Ahmed El-Attar, Samah Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title | Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title_full | Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title_fullStr | Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title_full_unstemmed | Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title_short | Effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
title_sort | effect of melatonin supplemented at the light or dark period on recovery of sciatic nerve injury in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379119/ https://www.ncbi.nlm.nih.gov/pubmed/28435433 http://dx.doi.org/10.17179/excli2016-763 |
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