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A novel excisional wound pain model for evaluation of analgesics in rats
BACKGROUND: Management of pain from open wounds is a growing unmet healthcare need. However, the models available to study pain from wounds or to develop analgesics for the patients suffering from them have primarily relied on incisional models. Here, we present the first characterized and validated...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019955/ https://www.ncbi.nlm.nih.gov/pubmed/33785668 http://dx.doi.org/10.3344/kjp.2021.34.2.165 |
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author | Parra, Sergio Thanawala, Vaidehi J. Rege, Ajay Giles, Heather |
author_facet | Parra, Sergio Thanawala, Vaidehi J. Rege, Ajay Giles, Heather |
author_sort | Parra, Sergio |
collection | PubMed |
description | BACKGROUND: Management of pain from open wounds is a growing unmet healthcare need. However, the models available to study pain from wounds or to develop analgesics for the patients suffering from them have primarily relied on incisional models. Here, we present the first characterized and validated model of open wound pain. METHODS: Unilateral full-skin excisional punch biopsy wounds on rat hind paws were evaluated for evoked pain using withdrawal responses to mechanical and thermal stimulation, and spontaneous pain was measured using hind paw weight distribution and guarding behavior. Evaluations were done before wounding (baseline) and 2-96 hours post-wounding. The model was validated by testing the effects of buprenorphine and carprofen. RESULTS: Pain responses to all tests increased within 2 hours post-wounding and were sustained for at least 4 days. Buprenorphine caused a reversal of all four pain responses at 1 and 4 hours post-treatment compared to 0.9% saline (P < 0.001). Carprofen decreased the pain response to thermal stimulation at 1 (P ≤ 0.049) and 4 hours (P < 0.011) post-treatment compared to 0.9% saline, but not to mechanical stimulation. CONCLUSIONS: This is the first well-characterized and validated model of pain from open wounds and will allow study of the pathophysiology of pain in open wounds and the development of wound-specific analgesics. |
format | Online Article Text |
id | pubmed-8019955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80199552021-04-13 A novel excisional wound pain model for evaluation of analgesics in rats Parra, Sergio Thanawala, Vaidehi J. Rege, Ajay Giles, Heather Korean J Pain Experimental Research Articles BACKGROUND: Management of pain from open wounds is a growing unmet healthcare need. However, the models available to study pain from wounds or to develop analgesics for the patients suffering from them have primarily relied on incisional models. Here, we present the first characterized and validated model of open wound pain. METHODS: Unilateral full-skin excisional punch biopsy wounds on rat hind paws were evaluated for evoked pain using withdrawal responses to mechanical and thermal stimulation, and spontaneous pain was measured using hind paw weight distribution and guarding behavior. Evaluations were done before wounding (baseline) and 2-96 hours post-wounding. The model was validated by testing the effects of buprenorphine and carprofen. RESULTS: Pain responses to all tests increased within 2 hours post-wounding and were sustained for at least 4 days. Buprenorphine caused a reversal of all four pain responses at 1 and 4 hours post-treatment compared to 0.9% saline (P < 0.001). Carprofen decreased the pain response to thermal stimulation at 1 (P ≤ 0.049) and 4 hours (P < 0.011) post-treatment compared to 0.9% saline, but not to mechanical stimulation. CONCLUSIONS: This is the first well-characterized and validated model of pain from open wounds and will allow study of the pathophysiology of pain in open wounds and the development of wound-specific analgesics. The Korean Pain Society 2021-04-01 2021-04-01 /pmc/articles/PMC8019955/ /pubmed/33785668 http://dx.doi.org/10.3344/kjp.2021.34.2.165 Text en © The Korean Pain Society, 2021 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Experimental Research Articles Parra, Sergio Thanawala, Vaidehi J. Rege, Ajay Giles, Heather A novel excisional wound pain model for evaluation of analgesics in rats |
title | A novel excisional wound pain model for evaluation of analgesics in rats |
title_full | A novel excisional wound pain model for evaluation of analgesics in rats |
title_fullStr | A novel excisional wound pain model for evaluation of analgesics in rats |
title_full_unstemmed | A novel excisional wound pain model for evaluation of analgesics in rats |
title_short | A novel excisional wound pain model for evaluation of analgesics in rats |
title_sort | novel excisional wound pain model for evaluation of analgesics in rats |
topic | Experimental Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019955/ https://www.ncbi.nlm.nih.gov/pubmed/33785668 http://dx.doi.org/10.3344/kjp.2021.34.2.165 |
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