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Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice
The use of botulinum neurotoxin-A (BoNT-A) is an alternative for the management of orofacial pain disorders. Although only Botox has labeled, there are other commercial brands available for use, among them: Dysport, Botulift, Prosigne, and Xeomin. The objective of the present study was to evaluate t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429966/ https://www.ncbi.nlm.nih.gov/pubmed/34527897 http://dx.doi.org/10.1016/j.toxcx.2021.100083 |
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author | Abrahão Cunha, Thays Crosara Gontijo Couto, Ana Claudia Januzzi, Eduardo Rosa Ferraz Gonçalves, Rafael Tardin Silva, Graziella Silva, Cassia Regina |
author_facet | Abrahão Cunha, Thays Crosara Gontijo Couto, Ana Claudia Januzzi, Eduardo Rosa Ferraz Gonçalves, Rafael Tardin Silva, Graziella Silva, Cassia Regina |
author_sort | Abrahão Cunha, Thays Crosara |
collection | PubMed |
description | The use of botulinum neurotoxin-A (BoNT-A) is an alternative for the management of orofacial pain disorders. Although only Botox has labeled, there are other commercial brands available for use, among them: Dysport, Botulift, Prosigne, and Xeomin. The objective of the present study was to evaluate the possible differences in the antinociceptive effect evoked by different commercially available formulations of BoNT-A in an animal model of inflammatory orofacial pain induced by formalin injection. Male C57/BL6 mice (20–25 g) were submitted to the pre-treatment with five different commercial brands of BoNT-A (Botox, Botulift, Xeomin, Dysport, or Prosigne; with doses between 0.02 and 0.2 Units of Botulinum Toxin, in 20 μL of 0.9% saline) three days prior the 2% formalin injection. All injections were made subcutaneously into the right perinasal area. After formalin injections, nociceptive behaviors like rubbing the place of injection were quantified during the neurogenic (0–5 min) and inflammatory (15–30 min) phases. The treatment using Botox, Botulift, and Xeomin were able to induce antinociceptive effects in both phases of the formalin-induced pain animal model, however, Dysport and Prosigne reduced the response in neither of them. Our data suggest that the treatment using different formulations of BoNT-A is not similar in efficacy as analgesics when evaluated in formalin-induced orofacial pain in mice. |
format | Online Article Text |
id | pubmed-8429966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-84299662021-09-14 Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice Abrahão Cunha, Thays Crosara Gontijo Couto, Ana Claudia Januzzi, Eduardo Rosa Ferraz Gonçalves, Rafael Tardin Silva, Graziella Silva, Cassia Regina Toxicon X Paper The use of botulinum neurotoxin-A (BoNT-A) is an alternative for the management of orofacial pain disorders. Although only Botox has labeled, there are other commercial brands available for use, among them: Dysport, Botulift, Prosigne, and Xeomin. The objective of the present study was to evaluate the possible differences in the antinociceptive effect evoked by different commercially available formulations of BoNT-A in an animal model of inflammatory orofacial pain induced by formalin injection. Male C57/BL6 mice (20–25 g) were submitted to the pre-treatment with five different commercial brands of BoNT-A (Botox, Botulift, Xeomin, Dysport, or Prosigne; with doses between 0.02 and 0.2 Units of Botulinum Toxin, in 20 μL of 0.9% saline) three days prior the 2% formalin injection. All injections were made subcutaneously into the right perinasal area. After formalin injections, nociceptive behaviors like rubbing the place of injection were quantified during the neurogenic (0–5 min) and inflammatory (15–30 min) phases. The treatment using Botox, Botulift, and Xeomin were able to induce antinociceptive effects in both phases of the formalin-induced pain animal model, however, Dysport and Prosigne reduced the response in neither of them. Our data suggest that the treatment using different formulations of BoNT-A is not similar in efficacy as analgesics when evaluated in formalin-induced orofacial pain in mice. Elsevier 2021-09-02 /pmc/articles/PMC8429966/ /pubmed/34527897 http://dx.doi.org/10.1016/j.toxcx.2021.100083 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Paper Abrahão Cunha, Thays Crosara Gontijo Couto, Ana Claudia Januzzi, Eduardo Rosa Ferraz Gonçalves, Rafael Tardin Silva, Graziella Silva, Cassia Regina Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title | Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title_full | Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title_fullStr | Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title_full_unstemmed | Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title_short | Analgesic potential of different available commercial brands of botulinum neurotoxin-A in formalin-induced orofacial pain in mice |
title_sort | analgesic potential of different available commercial brands of botulinum neurotoxin-a in formalin-induced orofacial pain in mice |
topic | Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429966/ https://www.ncbi.nlm.nih.gov/pubmed/34527897 http://dx.doi.org/10.1016/j.toxcx.2021.100083 |
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