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Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test
Objective(s): There are many reports about the role of rostral ventromedial medulla (RVM) in modulating stress-induced analgesia (SIA). In the previous study we demonstrated that temporal inactivation of RVM by lidocaine potentiated stress-induced analgesia. In this study, we investigated the effect...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016692/ https://www.ncbi.nlm.nih.gov/pubmed/24847424 |
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author | Shamsizadeh, Ali Soliemani, Neda Mohammad-Zadeh, Mohammad Azhdari-Zarmehri, Hassan |
author_facet | Shamsizadeh, Ali Soliemani, Neda Mohammad-Zadeh, Mohammad Azhdari-Zarmehri, Hassan |
author_sort | Shamsizadeh, Ali |
collection | PubMed |
description | Objective(s): There are many reports about the role of rostral ventromedial medulla (RVM) in modulating stress-induced analgesia (SIA). In the previous study we demonstrated that temporal inactivation of RVM by lidocaine potentiated stress-induced analgesia. In this study, we investigated the effect of permanent lesion of the RVM on SIA by using formalin test as a model of acute inflammatory pain. Materials and Methods: Three sets of experiments were conducted: (1) Application of stress protocol (2) Formalin injection after exposing the animals to the swim stress (3) Either the relevant vehicle or dopamine receptor 1 (D1) agonist R-SKF38393 was injected into the RVM to cause a lesion. For permanent lesion of RVM, R-SKF38393 was injected into the RVM. Forced swim stress in water was employed in adult male rats. Nociceptive responses were measured by formalin test (50µl injection of formalin 2% subcutaneously into hind paw) and pain related behaviors were monitored for 90 min. Results: In the unstressed rats, permanent lesion of the RVM by R-SKF38393 decreased formalin-induced nociceptive behaviors in phase 1, while in stressed rats, injection of R-SKF38393 into the RVM potentiated swim stress-induced antinociception in phase 1 and interphase, phase 2A of formalin test. Furthermore, R-SKF38393 had pronociceptive effects in phase2B whereas injections of R-SKF38393 resulted in significant difference in nociceptive bahaviours in all phases of formalin test (P<0.05). Conclusion: The result of the present study demonstrated that permanent inactivation of RVM can potentiate stress-induced analgesia in formalin test. |
format | Online Article Text |
id | pubmed-4016692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-40166922014-05-20 Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test Shamsizadeh, Ali Soliemani, Neda Mohammad-Zadeh, Mohammad Azhdari-Zarmehri, Hassan Iran J Basic Med Sci Original Article Objective(s): There are many reports about the role of rostral ventromedial medulla (RVM) in modulating stress-induced analgesia (SIA). In the previous study we demonstrated that temporal inactivation of RVM by lidocaine potentiated stress-induced analgesia. In this study, we investigated the effect of permanent lesion of the RVM on SIA by using formalin test as a model of acute inflammatory pain. Materials and Methods: Three sets of experiments were conducted: (1) Application of stress protocol (2) Formalin injection after exposing the animals to the swim stress (3) Either the relevant vehicle or dopamine receptor 1 (D1) agonist R-SKF38393 was injected into the RVM to cause a lesion. For permanent lesion of RVM, R-SKF38393 was injected into the RVM. Forced swim stress in water was employed in adult male rats. Nociceptive responses were measured by formalin test (50µl injection of formalin 2% subcutaneously into hind paw) and pain related behaviors were monitored for 90 min. Results: In the unstressed rats, permanent lesion of the RVM by R-SKF38393 decreased formalin-induced nociceptive behaviors in phase 1, while in stressed rats, injection of R-SKF38393 into the RVM potentiated swim stress-induced antinociception in phase 1 and interphase, phase 2A of formalin test. Furthermore, R-SKF38393 had pronociceptive effects in phase2B whereas injections of R-SKF38393 resulted in significant difference in nociceptive bahaviours in all phases of formalin test (P<0.05). Conclusion: The result of the present study demonstrated that permanent inactivation of RVM can potentiate stress-induced analgesia in formalin test. Mashhad University of Medical Sciences 2014-03 /pmc/articles/PMC4016692/ /pubmed/24847424 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shamsizadeh, Ali Soliemani, Neda Mohammad-Zadeh, Mohammad Azhdari-Zarmehri, Hassan Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title | Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title_full | Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title_fullStr | Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title_full_unstemmed | Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title_short | Permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
title_sort | permanent lesion in rostral ventromedial medulla potentiates swim stress-induced analgesia in formalin test |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016692/ https://www.ncbi.nlm.nih.gov/pubmed/24847424 |
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