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Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain

PURPOSE: Baclofen and morphine have shown efficacy against mechanical allodynia after infraorbital nerve chronic constriction injury (IoN-CCI). No drug effects have yet been reported on spontaneous trigeminal neuropathic pain. It has been proposed that the directed face grooming behavior that also d...

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Autores principales: Deseure, K, Hans, GH
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291328/
https://www.ncbi.nlm.nih.gov/pubmed/28184169
http://dx.doi.org/10.2147/JPR.S124526
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author Deseure, K
Hans, GH
author_facet Deseure, K
Hans, GH
author_sort Deseure, K
collection PubMed
description PURPOSE: Baclofen and morphine have shown efficacy against mechanical allodynia after infraorbital nerve chronic constriction injury (IoN-CCI). No drug effects have yet been reported on spontaneous trigeminal neuropathic pain. It has been proposed that the directed face grooming behavior that also develops following IoN-CCI offers a measure of spontaneous trigeminal neuropathic pain. SUBJECTS AND METHODS: We examined the effects of a continuous 1-week infusion of 30 mg/day carbamazepine (the first-line drug treatment for trigeminal neuralgia), 1.06 mg/day baclofen, 4.18 mg/day clomipramine, and 5 mg/day morphine on spontaneous and mechanically evoked pain behavior (ie, directed face grooming and von Frey testing) in IoN-CCI rats. RESULTS: Isolated face grooming was significantly reduced in rats receiving carbamazepine and baclofen but not in clomipramine- or morphine-treated rats. All drugs showed significant antiallodynic effects; carbamazepine showed the strongest effects, whereas clomipramine had only minor efficacy. CONCLUSION: The tested drugs have differential effects in the IoN-CCI model, and different neuropathological mechanisms may underlie the different somatosensory symptoms in this model. A mechanism-based approach may be needed to treat (trigeminal) neuropathic pain. The present data support IoN-CCI as a model of trigeminal neuralgia in which isolated face grooming is used as a measure of spontaneous neuropathic pain.
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spelling pubmed-52913282017-02-09 Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain Deseure, K Hans, GH J Pain Res Original Research PURPOSE: Baclofen and morphine have shown efficacy against mechanical allodynia after infraorbital nerve chronic constriction injury (IoN-CCI). No drug effects have yet been reported on spontaneous trigeminal neuropathic pain. It has been proposed that the directed face grooming behavior that also develops following IoN-CCI offers a measure of spontaneous trigeminal neuropathic pain. SUBJECTS AND METHODS: We examined the effects of a continuous 1-week infusion of 30 mg/day carbamazepine (the first-line drug treatment for trigeminal neuralgia), 1.06 mg/day baclofen, 4.18 mg/day clomipramine, and 5 mg/day morphine on spontaneous and mechanically evoked pain behavior (ie, directed face grooming and von Frey testing) in IoN-CCI rats. RESULTS: Isolated face grooming was significantly reduced in rats receiving carbamazepine and baclofen but not in clomipramine- or morphine-treated rats. All drugs showed significant antiallodynic effects; carbamazepine showed the strongest effects, whereas clomipramine had only minor efficacy. CONCLUSION: The tested drugs have differential effects in the IoN-CCI model, and different neuropathological mechanisms may underlie the different somatosensory symptoms in this model. A mechanism-based approach may be needed to treat (trigeminal) neuropathic pain. The present data support IoN-CCI as a model of trigeminal neuralgia in which isolated face grooming is used as a measure of spontaneous neuropathic pain. Dove Medical Press 2017-01-27 /pmc/articles/PMC5291328/ /pubmed/28184169 http://dx.doi.org/10.2147/JPR.S124526 Text en © 2017 Deseure and Hans. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. 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
Deseure, K
Hans, GH
Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title_full Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title_fullStr Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title_full_unstemmed Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title_short Differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
title_sort differential drug effects on spontaneous and evoked pain behavior in a model of trigeminal neuropathic pain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291328/
https://www.ncbi.nlm.nih.gov/pubmed/28184169
http://dx.doi.org/10.2147/JPR.S124526
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