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Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats

BACKGROUND: The neural mobilization technique is a noninvasive method that has proved clinically effective in reducing pain sensitivity and consequently in improving quality of life after neuropathic pain. The present study examined the effects of neural mobilization (NM) on pain sensitivity induced...

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Autores principales: Santos, Fabio M, Silva, Joyce T, Giardini, Aline C, Rocha, Priscila A, Achermann, Arnold PP, S Alves, Adilson, Britto, Luiz RG, Chacur, Marucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495676/
https://www.ncbi.nlm.nih.gov/pubmed/22839415
http://dx.doi.org/10.1186/1744-8069-8-57
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author Santos, Fabio M
Silva, Joyce T
Giardini, Aline C
Rocha, Priscila A
Achermann, Arnold PP
S Alves, Adilson
Britto, Luiz RG
Chacur, Marucia
author_facet Santos, Fabio M
Silva, Joyce T
Giardini, Aline C
Rocha, Priscila A
Achermann, Arnold PP
S Alves, Adilson
Britto, Luiz RG
Chacur, Marucia
author_sort Santos, Fabio M
collection PubMed
description BACKGROUND: The neural mobilization technique is a noninvasive method that has proved clinically effective in reducing pain sensitivity and consequently in improving quality of life after neuropathic pain. The present study examined the effects of neural mobilization (NM) on pain sensitivity induced by chronic constriction injury (CCI) in rats. The CCI was performed on adult male rats, submitted thereafter to 10 sessions of NM, each other day, starting 14 days after the CCI injury. Over the treatment period, animals were evaluated for nociception using behavioral tests, such as tests for allodynia and thermal and mechanical hyperalgesia. At the end of the sessions, the dorsal root ganglion (DRG) and spinal cord were analyzed using immunohistochemistry and Western blot assays for neural growth factor (NGF) and glial fibrillary acidic protein (GFAP). RESULTS: The NM treatment induced an early reduction (from the second session) of the hyperalgesia and allodynia in CCI-injured rats, which persisted until the end of the treatment. On the other hand, only after the 4(th) session we observed a blockade of thermal sensitivity. Regarding cellular changes, we observed a decrease of GFAP and NGF expression after NM in the ipsilateral DRG (68% and 111%, respectively) and the decrease of only GFAP expression after NM in the lumbar spinal cord (L3-L6) (108%). CONCLUSIONS: These data provide evidence that NM treatment reverses pain symptoms in CCI-injured rats and suggest the involvement of glial cells and NGF in such an effect.
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spelling pubmed-34956762012-11-13 Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats Santos, Fabio M Silva, Joyce T Giardini, Aline C Rocha, Priscila A Achermann, Arnold PP S Alves, Adilson Britto, Luiz RG Chacur, Marucia Mol Pain Research BACKGROUND: The neural mobilization technique is a noninvasive method that has proved clinically effective in reducing pain sensitivity and consequently in improving quality of life after neuropathic pain. The present study examined the effects of neural mobilization (NM) on pain sensitivity induced by chronic constriction injury (CCI) in rats. The CCI was performed on adult male rats, submitted thereafter to 10 sessions of NM, each other day, starting 14 days after the CCI injury. Over the treatment period, animals were evaluated for nociception using behavioral tests, such as tests for allodynia and thermal and mechanical hyperalgesia. At the end of the sessions, the dorsal root ganglion (DRG) and spinal cord were analyzed using immunohistochemistry and Western blot assays for neural growth factor (NGF) and glial fibrillary acidic protein (GFAP). RESULTS: The NM treatment induced an early reduction (from the second session) of the hyperalgesia and allodynia in CCI-injured rats, which persisted until the end of the treatment. On the other hand, only after the 4(th) session we observed a blockade of thermal sensitivity. Regarding cellular changes, we observed a decrease of GFAP and NGF expression after NM in the ipsilateral DRG (68% and 111%, respectively) and the decrease of only GFAP expression after NM in the lumbar spinal cord (L3-L6) (108%). CONCLUSIONS: These data provide evidence that NM treatment reverses pain symptoms in CCI-injured rats and suggest the involvement of glial cells and NGF in such an effect. BioMed Central 2012-07-29 /pmc/articles/PMC3495676/ /pubmed/22839415 http://dx.doi.org/10.1186/1744-8069-8-57 Text en Copyright ©2012 Santos et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Santos, Fabio M
Silva, Joyce T
Giardini, Aline C
Rocha, Priscila A
Achermann, Arnold PP
S Alves, Adilson
Britto, Luiz RG
Chacur, Marucia
Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title_full Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title_fullStr Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title_full_unstemmed Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title_short Neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
title_sort neural mobilization reverses behavioral and cellular changes that characterize neuropathic pain in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495676/
https://www.ncbi.nlm.nih.gov/pubmed/22839415
http://dx.doi.org/10.1186/1744-8069-8-57
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