Cargando…
Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats
PURPOSE: The treatment of central neuropathic pain remains amongst the biggest challenges for pain specialists. The main objective of this study was to assess gabapentin (GBP), amitriptyline (AMI), and carbamazepine (CARBA) for the treatment of a rodent central neuropathic pain model. METHODS: Male...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869939/ https://www.ncbi.nlm.nih.gov/pubmed/24368890 http://dx.doi.org/10.2147/JPR.S55201 |
_version_ | 1782296641137541120 |
---|---|
author | Castel, Aude Vachon, Pascal |
author_facet | Castel, Aude Vachon, Pascal |
author_sort | Castel, Aude |
collection | PubMed |
description | PURPOSE: The treatment of central neuropathic pain remains amongst the biggest challenges for pain specialists. The main objective of this study was to assess gabapentin (GBP), amitriptyline (AMI), and carbamazepine (CARBA) for the treatment of a rodent central neuropathic pain model. METHODS: Male Sprague Dawley rats were trained on the rotarod, Hargreaves, Von Frey and acetone behavioral tests, and baseline values were obtained prior to surgery. A stereotaxic injection of either a collagenase solution or saline was made in the right ventral posterolateral thalamic nucleus. The rats were tested on days 2, 4, 8, and 11 postsurgery. They were retested at regular intervals from day 15 to day 25 postsurgery, after oral administration of either the vehicle (n=7 and n=8 rats with intracerebral injections of collagenase and saline, respectively) or the different drugs (GBP [60 mg/kg], AMI [10 mg/kg], CARBA [100 mg/kg]; n=8 rats/drug). RESULTS: A significant decrease in the mechanical thresholds and no change in heat threshold were observed in both hind limbs in the collagenase group, as we had previously shown elsewhere. Reversal of the mechanical hypersensitivity was achieved only with GBP (P<0.05). AMI and CARBA, at the dosages used, failed to show any effect on mechanical thresholds. Transient cold allodynia was observed in some collagenase-injected rats but failed to be statistically significant. CONCLUSION: Intrathalamic hemorrhaging in the ventrolateral thalamic nucleus induced a bilateral mechanical allodynia, which was reversed by GBP but not AMI or CARBA. |
format | Online Article Text |
id | pubmed-3869939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38699392013-12-24 Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats Castel, Aude Vachon, Pascal J Pain Res Original Research PURPOSE: The treatment of central neuropathic pain remains amongst the biggest challenges for pain specialists. The main objective of this study was to assess gabapentin (GBP), amitriptyline (AMI), and carbamazepine (CARBA) for the treatment of a rodent central neuropathic pain model. METHODS: Male Sprague Dawley rats were trained on the rotarod, Hargreaves, Von Frey and acetone behavioral tests, and baseline values were obtained prior to surgery. A stereotaxic injection of either a collagenase solution or saline was made in the right ventral posterolateral thalamic nucleus. The rats were tested on days 2, 4, 8, and 11 postsurgery. They were retested at regular intervals from day 15 to day 25 postsurgery, after oral administration of either the vehicle (n=7 and n=8 rats with intracerebral injections of collagenase and saline, respectively) or the different drugs (GBP [60 mg/kg], AMI [10 mg/kg], CARBA [100 mg/kg]; n=8 rats/drug). RESULTS: A significant decrease in the mechanical thresholds and no change in heat threshold were observed in both hind limbs in the collagenase group, as we had previously shown elsewhere. Reversal of the mechanical hypersensitivity was achieved only with GBP (P<0.05). AMI and CARBA, at the dosages used, failed to show any effect on mechanical thresholds. Transient cold allodynia was observed in some collagenase-injected rats but failed to be statistically significant. CONCLUSION: Intrathalamic hemorrhaging in the ventrolateral thalamic nucleus induced a bilateral mechanical allodynia, which was reversed by GBP but not AMI or CARBA. Dove Medical Press 2013-12-17 /pmc/articles/PMC3869939/ /pubmed/24368890 http://dx.doi.org/10.2147/JPR.S55201 Text en © 2014 Castel and Vachon. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Castel, Aude Vachon, Pascal Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title | Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title_full | Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title_fullStr | Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title_full_unstemmed | Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title_short | Gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
title_sort | gabapentin reverses central pain sensitization following a collagenase-induced intrathalamic hemorrhage in rats |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869939/ https://www.ncbi.nlm.nih.gov/pubmed/24368890 http://dx.doi.org/10.2147/JPR.S55201 |
work_keys_str_mv | AT castelaude gabapentinreversescentralpainsensitizationfollowingacollagenaseinducedintrathalamichemorrhageinrats AT vachonpascal gabapentinreversescentralpainsensitizationfollowingacollagenaseinducedintrathalamichemorrhageinrats |