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Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain

BACKGROUND AND THE PURPOSE OF THE STUDY: Pentoxifylline (PTX) is a non-specific cytokite pain in several animal models and humans. However, long-term therapeutic effects of PTX on neuropathic pain in a rat model of chronic constriction injury (CCI) are not completely clear. This study was conducted...

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Autores principales: Vakili, A., Shirvanian, MJ., Safakhah, HA., Rashidy-Pour, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304381/
https://www.ncbi.nlm.nih.gov/pubmed/22615674
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author Vakili, A.
Shirvanian, MJ.
Safakhah, HA.
Rashidy-Pour, A.
author_facet Vakili, A.
Shirvanian, MJ.
Safakhah, HA.
Rashidy-Pour, A.
author_sort Vakili, A.
collection PubMed
description BACKGROUND AND THE PURPOSE OF THE STUDY: Pentoxifylline (PTX) is a non-specific cytokite pain in several animal models and humans. However, long-term therapeutic effects of PTX on neuropathic pain in a rat model of chronic constriction injury (CCI) are not completely clear. This study was conducted to examine the effect of long-term administration of PTX on neuropathic pain in rats. METHODS: Neuropathic pain was induced by sciatic nerve ligation using of CCI model in rats. Rats were randomly assigned into sham, CCI-saline treated, and CCI-PTX treated (30 or 60 mg/kg ip) groups. PTX or saline administered at 30 min before CCI and daily for 14 days post-CCI. At the days of 3, 7, 11 and 14 following CCI, by using standard methods effects of thermal hyperalgesia, thermal and mechanical allodynia in all groups were examined using the standard methods. RESULTS: The CCI-saline treated group showed a significant increase in mechanical and thermal allodynia, and thermal hyperalgesia as compared with the sham group in the tested days. Administration of the higher dose of PTX (60 mg/kg/day), but not the lower dose (30 mg/kg/day) significantly reduced mechanical and thermal allodynia, as compared with the CCI–saline treated group on days of 3, 7, 11 and 14 (all P values<0.001). Also, both doses of PTX significantly reduced thermal hyperalgesia as compared with the CCI-saline treated group on these days (all P values<0.001). CONCLUSION: Results of this study show that chronic administration of PTX reduces the neuropathic pain in a rat model of CCI. Thus, this drug may have a therapeutic application in the treatment and management of neuropathic pain in humans.
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spelling pubmed-33043812012-05-21 Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain Vakili, A. Shirvanian, MJ. Safakhah, HA. Rashidy-Pour, A. Daru Original Article BACKGROUND AND THE PURPOSE OF THE STUDY: Pentoxifylline (PTX) is a non-specific cytokite pain in several animal models and humans. However, long-term therapeutic effects of PTX on neuropathic pain in a rat model of chronic constriction injury (CCI) are not completely clear. This study was conducted to examine the effect of long-term administration of PTX on neuropathic pain in rats. METHODS: Neuropathic pain was induced by sciatic nerve ligation using of CCI model in rats. Rats were randomly assigned into sham, CCI-saline treated, and CCI-PTX treated (30 or 60 mg/kg ip) groups. PTX or saline administered at 30 min before CCI and daily for 14 days post-CCI. At the days of 3, 7, 11 and 14 following CCI, by using standard methods effects of thermal hyperalgesia, thermal and mechanical allodynia in all groups were examined using the standard methods. RESULTS: The CCI-saline treated group showed a significant increase in mechanical and thermal allodynia, and thermal hyperalgesia as compared with the sham group in the tested days. Administration of the higher dose of PTX (60 mg/kg/day), but not the lower dose (30 mg/kg/day) significantly reduced mechanical and thermal allodynia, as compared with the CCI–saline treated group on days of 3, 7, 11 and 14 (all P values<0.001). Also, both doses of PTX significantly reduced thermal hyperalgesia as compared with the CCI-saline treated group on these days (all P values<0.001). CONCLUSION: Results of this study show that chronic administration of PTX reduces the neuropathic pain in a rat model of CCI. Thus, this drug may have a therapeutic application in the treatment and management of neuropathic pain in humans. Tehran University of Medical Sciences 2011 /pmc/articles/PMC3304381/ /pubmed/22615674 Text en © 2011 Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Vakili, A.
Shirvanian, MJ.
Safakhah, HA.
Rashidy-Pour, A.
Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title_full Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title_fullStr Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title_full_unstemmed Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title_short Pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
title_sort pentoxifylline decreases allodynia and hyperalgesia in a rat model of neuropathic pain
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304381/
https://www.ncbi.nlm.nih.gov/pubmed/22615674
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