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Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation
OBJECTIVE(S): Neurotrophins (NTs) exert various effects on neuronal system. Growing evidence indicates that NTs are involved in the pathophysiology of neuropathic pain. However, the exact role of these proteins in modulating nociceptive signaling requires being defined. Thus, the aim of this study w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243971/ https://www.ncbi.nlm.nih.gov/pubmed/28133521 http://dx.doi.org/10.22038/ijbms.2017.8089 |
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author | Kazemi, Abdolreza Rahmati, Masoud Eslami, Rasoul Sheibani, Vahid |
author_facet | Kazemi, Abdolreza Rahmati, Masoud Eslami, Rasoul Sheibani, Vahid |
author_sort | Kazemi, Abdolreza |
collection | PubMed |
description | OBJECTIVE(S): Neurotrophins (NTs) exert various effects on neuronal system. Growing evidence indicates that NTs are involved in the pathophysiology of neuropathic pain. However, the exact role of these proteins in modulating nociceptive signaling requires being defined. Thus, the aim of this study was to evaluate the effects of spinal nerve ligation (SNL) on NTs activation in the lumbar dorsal root. MATERIALS AND METHODS: Ten male Wistar rats were randomly assigned to two groups: tight ligation of the L5 spinal nerve (SNL: n=5) and Sham (n=5). In order to produce neuropathic pain, the L5 spinal nerve was tightly ligated (SNL). Then, allodynia and hyperalgesia tests were conducted weekly. After 4 weeks, tissue samples were taken from the two groups for laboratory evaluations. Here, Real-Time PCR quantity method was used for measuring NTs gene expression levels. RESULTS: SNL resulted in a significant weight loss in the soleus muscle (P<0.05), mechanical allodynia and thermal hyperalgesia thresholds (respectively, P<0.05; P<0.05). Also, NGF, NT-4, NT-3, TrkA, TrkB and TrkC expression were up-regulated following spinal nerve ligation group (respectively, P=0.025, P=0.013, P=0.001, P=0.002, P<0.001, P=001) (respectively, 4.7, 5.2, 7.5, 5.1, 7.2, 6.2 folds). CONCLUSION: The present study provides new evidence that neuropathic pain induced by spinal nerve ligation probably activates NTs and Trk receptors expression in DRG. However, further studies are needed to better elucidate the role of NTs in a neuropathic pain. |
format | Online Article Text |
id | pubmed-5243971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-52439712017-01-27 Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation Kazemi, Abdolreza Rahmati, Masoud Eslami, Rasoul Sheibani, Vahid Iran J Basic Med Sci Original Article OBJECTIVE(S): Neurotrophins (NTs) exert various effects on neuronal system. Growing evidence indicates that NTs are involved in the pathophysiology of neuropathic pain. However, the exact role of these proteins in modulating nociceptive signaling requires being defined. Thus, the aim of this study was to evaluate the effects of spinal nerve ligation (SNL) on NTs activation in the lumbar dorsal root. MATERIALS AND METHODS: Ten male Wistar rats were randomly assigned to two groups: tight ligation of the L5 spinal nerve (SNL: n=5) and Sham (n=5). In order to produce neuropathic pain, the L5 spinal nerve was tightly ligated (SNL). Then, allodynia and hyperalgesia tests were conducted weekly. After 4 weeks, tissue samples were taken from the two groups for laboratory evaluations. Here, Real-Time PCR quantity method was used for measuring NTs gene expression levels. RESULTS: SNL resulted in a significant weight loss in the soleus muscle (P<0.05), mechanical allodynia and thermal hyperalgesia thresholds (respectively, P<0.05; P<0.05). Also, NGF, NT-4, NT-3, TrkA, TrkB and TrkC expression were up-regulated following spinal nerve ligation group (respectively, P=0.025, P=0.013, P=0.001, P=0.002, P<0.001, P=001) (respectively, 4.7, 5.2, 7.5, 5.1, 7.2, 6.2 folds). CONCLUSION: The present study provides new evidence that neuropathic pain induced by spinal nerve ligation probably activates NTs and Trk receptors expression in DRG. However, further studies are needed to better elucidate the role of NTs in a neuropathic pain. Mashhad University of Medical Sciences 2017-01 /pmc/articles/PMC5243971/ /pubmed/28133521 http://dx.doi.org/10.22038/ijbms.2017.8089 Text en Copyright: © Iranian Journal of Basic Medical Sciences 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 | Original Article Kazemi, Abdolreza Rahmati, Masoud Eslami, Rasoul Sheibani, Vahid Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title | Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title_full | Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title_fullStr | Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title_full_unstemmed | Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title_short | Activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
title_sort | activation of neurotrophins in lumbar dorsal root probably contributes to neuropathic pain after spinal nerve ligation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243971/ https://www.ncbi.nlm.nih.gov/pubmed/28133521 http://dx.doi.org/10.22038/ijbms.2017.8089 |
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