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Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy
Nucleus pulposus (NP) has been suggested to trigger an autoimmune response if exposed to the immune system, which plays a key role in neuropathic pain. Therefore, appropriate suppression of inflammation is a key factor for treating the radiculopathy caused by intervertebral disk (IVD) degeneration....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228059/ https://www.ncbi.nlm.nih.gov/pubmed/28101174 http://dx.doi.org/10.3892/etm.2016.3878 |
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author | Lin, Bin Yu, Hui He, Yongzhi Xu, Yang Zhang, Wenbin Lu, Chengwu Ao, Qingfang |
author_facet | Lin, Bin Yu, Hui He, Yongzhi Xu, Yang Zhang, Wenbin Lu, Chengwu Ao, Qingfang |
author_sort | Lin, Bin |
collection | PubMed |
description | Nucleus pulposus (NP) has been suggested to trigger an autoimmune response if exposed to the immune system, which plays a key role in neuropathic pain. Therefore, appropriate suppression of inflammation is a key factor for treating the radiculopathy caused by intervertebral disk (IVD) degeneration. Resveratrol, a key component of red wine, has been suggested to exhibit anti-inflammatory properties in vitro and in vivo. However, the effects of resveratrol on NP-mediated pain in vivo have not been studied. The aim of the present study was to investigate whether resveratrol may be useful in treating NP-mediated pain in an autologous NP model of radiculopathy. A total of 36 adult male Sprague-Dawley rats were allocated randomly into sham (group I), saline-treated (group II) and resveratrol-treated (group III) groups. Animal behavior in response to non-noxious mechanical stimulation with von Frey filaments was compared at days 0 (baseline), 3, 7, 14 and 21 following surgery. The expression of proinflammatory cytokines such as tumor necrosis factor α (TNF-α) and interleukin-1 (IL-1) were assessed at days 7 and 14. The data showed that resveratrol exhibited an anti-inflammatory effect on the expression of proinflammatory cytokines. Compared with group II, the expression of TNF-α and IL-1 was significantly decreased at each time point in group III. In addition, resveratrol significantly reduced pain behavior triggered by the application of NP tissue on the dorsal root ganglion for up to 14 days. These data suggest that resveratrol has potential for the treatment of NP-mediated pain, indicating a potential clinical application. |
format | Online Article Text |
id | pubmed-5228059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-52280592017-01-18 Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy Lin, Bin Yu, Hui He, Yongzhi Xu, Yang Zhang, Wenbin Lu, Chengwu Ao, Qingfang Exp Ther Med Articles Nucleus pulposus (NP) has been suggested to trigger an autoimmune response if exposed to the immune system, which plays a key role in neuropathic pain. Therefore, appropriate suppression of inflammation is a key factor for treating the radiculopathy caused by intervertebral disk (IVD) degeneration. Resveratrol, a key component of red wine, has been suggested to exhibit anti-inflammatory properties in vitro and in vivo. However, the effects of resveratrol on NP-mediated pain in vivo have not been studied. The aim of the present study was to investigate whether resveratrol may be useful in treating NP-mediated pain in an autologous NP model of radiculopathy. A total of 36 adult male Sprague-Dawley rats were allocated randomly into sham (group I), saline-treated (group II) and resveratrol-treated (group III) groups. Animal behavior in response to non-noxious mechanical stimulation with von Frey filaments was compared at days 0 (baseline), 3, 7, 14 and 21 following surgery. The expression of proinflammatory cytokines such as tumor necrosis factor α (TNF-α) and interleukin-1 (IL-1) were assessed at days 7 and 14. The data showed that resveratrol exhibited an anti-inflammatory effect on the expression of proinflammatory cytokines. Compared with group II, the expression of TNF-α and IL-1 was significantly decreased at each time point in group III. In addition, resveratrol significantly reduced pain behavior triggered by the application of NP tissue on the dorsal root ganglion for up to 14 days. These data suggest that resveratrol has potential for the treatment of NP-mediated pain, indicating a potential clinical application. D.A. Spandidos 2016-12 2016-11-07 /pmc/articles/PMC5228059/ /pubmed/28101174 http://dx.doi.org/10.3892/etm.2016.3878 Text en Copyright: © Lin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Lin, Bin Yu, Hui He, Yongzhi Xu, Yang Zhang, Wenbin Lu, Chengwu Ao, Qingfang Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title | Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title_full | Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title_fullStr | Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title_full_unstemmed | Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title_short | Protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
title_sort | protective effects of resveratrol on autologous nucleus pulposus model of radiculopathy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228059/ https://www.ncbi.nlm.nih.gov/pubmed/28101174 http://dx.doi.org/10.3892/etm.2016.3878 |
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