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Objective validation of central sensitization in the rat UVB and heat rekindling model
BACKGROUND: The UVB and heat rekindling (UVB/HR) model shows potential as a translatable inflammatory pain model. However, the occurrence of central sensitization in this model, a fundamental mechanism underlying chronic pain, has been debated. Face, construct and predictive validity are key requisi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232048/ https://www.ncbi.nlm.nih.gov/pubmed/24590815 http://dx.doi.org/10.1002/j.1532-2149.2014.00469.x |
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author | Weerasinghe, NS Lumb, BM Apps, R Koutsikou, S Murrell, JC |
author_facet | Weerasinghe, NS Lumb, BM Apps, R Koutsikou, S Murrell, JC |
author_sort | Weerasinghe, NS |
collection | PubMed |
description | BACKGROUND: The UVB and heat rekindling (UVB/HR) model shows potential as a translatable inflammatory pain model. However, the occurrence of central sensitization in this model, a fundamental mechanism underlying chronic pain, has been debated. Face, construct and predictive validity are key requisites of animal models; electromyogram (EMG) recordings were utilized to objectively demonstrate validity of the rat UVB/HR model. METHODS: The UVB/HR model was induced on the heel of the hind paw under anaesthesia. Mechanical withdrawal thresholds (MWTs) were obtained from biceps femoris EMG responses to a gradually increasing pinch at the mid hind paw region under alfaxalone anaesthesia, 96 h after UVB irradiation. MWT was compared between UVB/HR and SHAM-treated rats (anaesthetic only). Underlying central mechanisms in the model were pharmacologically validated by MWT measurement following intrathecal N-methyl-d-aspartate (NMDA) receptor antagonist, MK-801, or saline. RESULTS: Secondary hyperalgesia was confirmed by a significantly lower pre-drug MWT {mean [±standard error of the mean (SEM)]} in UVB/HR [56.3 (±2.1) g/mm(2), n = 15] compared with SHAM-treated rats [69.3 (±2.9) g/mm(2), n = 8], confirming face validity of the model. Predictive validity was demonstrated by the attenuation of secondary hyperalgesia by MK-801, where mean (±SEM) MWT was significantly higher [77.2 (±5.9) g/mm(2) n = 7] in comparison with pre-drug [57.8 (±3.5) g/mm(2) n = 7] and saline [57.0 (±3.2) g/mm(2) n = 8] at peak drug effect. The occurrence of central sensitization confirmed construct validity of the UVB/HR model. CONCLUSIONS: This study used objective outcome measures of secondary hyperalgesia to validate the rat UVB/HR model as a translational model of inflammatory pain. WHAT'S ALREADY KNOWN ABOUT THIS TOPIC? Most current animal chronic pain models lack translatability to human subjects. Primary hyperalgesia is an established feature of the UVB/heat rekindling inflammatory pain model in rodents and humans, but the presence of secondary hyperalgesia, a hallmark feature of central sensitization and thus chronic pain, is contentious. WHAT DOES THIS STUDY ADD? Secondary hyperalgesia was demonstrated in the rat UVB/heat rekindling model using an objective outcome measure (electromyogram), overcoming the subjective limitations of previous behavioural studies. |
format | Online Article Text |
id | pubmed-4232048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42320482014-12-15 Objective validation of central sensitization in the rat UVB and heat rekindling model Weerasinghe, NS Lumb, BM Apps, R Koutsikou, S Murrell, JC Eur J Pain New Research BACKGROUND: The UVB and heat rekindling (UVB/HR) model shows potential as a translatable inflammatory pain model. However, the occurrence of central sensitization in this model, a fundamental mechanism underlying chronic pain, has been debated. Face, construct and predictive validity are key requisites of animal models; electromyogram (EMG) recordings were utilized to objectively demonstrate validity of the rat UVB/HR model. METHODS: The UVB/HR model was induced on the heel of the hind paw under anaesthesia. Mechanical withdrawal thresholds (MWTs) were obtained from biceps femoris EMG responses to a gradually increasing pinch at the mid hind paw region under alfaxalone anaesthesia, 96 h after UVB irradiation. MWT was compared between UVB/HR and SHAM-treated rats (anaesthetic only). Underlying central mechanisms in the model were pharmacologically validated by MWT measurement following intrathecal N-methyl-d-aspartate (NMDA) receptor antagonist, MK-801, or saline. RESULTS: Secondary hyperalgesia was confirmed by a significantly lower pre-drug MWT {mean [±standard error of the mean (SEM)]} in UVB/HR [56.3 (±2.1) g/mm(2), n = 15] compared with SHAM-treated rats [69.3 (±2.9) g/mm(2), n = 8], confirming face validity of the model. Predictive validity was demonstrated by the attenuation of secondary hyperalgesia by MK-801, where mean (±SEM) MWT was significantly higher [77.2 (±5.9) g/mm(2) n = 7] in comparison with pre-drug [57.8 (±3.5) g/mm(2) n = 7] and saline [57.0 (±3.2) g/mm(2) n = 8] at peak drug effect. The occurrence of central sensitization confirmed construct validity of the UVB/HR model. CONCLUSIONS: This study used objective outcome measures of secondary hyperalgesia to validate the rat UVB/HR model as a translational model of inflammatory pain. WHAT'S ALREADY KNOWN ABOUT THIS TOPIC? Most current animal chronic pain models lack translatability to human subjects. Primary hyperalgesia is an established feature of the UVB/heat rekindling inflammatory pain model in rodents and humans, but the presence of secondary hyperalgesia, a hallmark feature of central sensitization and thus chronic pain, is contentious. WHAT DOES THIS STUDY ADD? Secondary hyperalgesia was demonstrated in the rat UVB/heat rekindling model using an objective outcome measure (electromyogram), overcoming the subjective limitations of previous behavioural studies. BlackWell Publishing Ltd 2014-09 2014-03-03 /pmc/articles/PMC4232048/ /pubmed/24590815 http://dx.doi.org/10.1002/j.1532-2149.2014.00469.x Text en Copyright © 2014 European Pain Federation - EFIC® http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | New Research Weerasinghe, NS Lumb, BM Apps, R Koutsikou, S Murrell, JC Objective validation of central sensitization in the rat UVB and heat rekindling model |
title | Objective validation of central sensitization in the rat UVB and heat rekindling model |
title_full | Objective validation of central sensitization in the rat UVB and heat rekindling model |
title_fullStr | Objective validation of central sensitization in the rat UVB and heat rekindling model |
title_full_unstemmed | Objective validation of central sensitization in the rat UVB and heat rekindling model |
title_short | Objective validation of central sensitization in the rat UVB and heat rekindling model |
title_sort | objective validation of central sensitization in the rat uvb and heat rekindling model |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232048/ https://www.ncbi.nlm.nih.gov/pubmed/24590815 http://dx.doi.org/10.1002/j.1532-2149.2014.00469.x |
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