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Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice
BACKGROUND: Scalding burn injuries can occur in everyday life but occur more frequently in young children. Therefore, it is important to develop more effective burn treatments. OBJECTIVES: This study examined the effects of bee venom (BV) stimulation on scalding burn injury-induced nociception in mi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Veterinary Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850793/ https://www.ncbi.nlm.nih.gov/pubmed/33522161 http://dx.doi.org/10.4142/jvs.2021.22.e9 |
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author | Kang, Dong-Wook Choi, Jae-Gyun Kim, Jaehyuk Park, Jin Bong Lee, Jang-Hern Kim, Hyun-Woo |
author_facet | Kang, Dong-Wook Choi, Jae-Gyun Kim, Jaehyuk Park, Jin Bong Lee, Jang-Hern Kim, Hyun-Woo |
author_sort | Kang, Dong-Wook |
collection | PubMed |
description | BACKGROUND: Scalding burn injuries can occur in everyday life but occur more frequently in young children. Therefore, it is important to develop more effective burn treatments. OBJECTIVES: This study examined the effects of bee venom (BV) stimulation on scalding burn injury-induced nociception in mice as a new treatment for burn pain. METHODS: To develop a burn injury model, the right hind paw was immersed temporarily in hot water (65°C, 3 seconds). Immediately after the burn, BV (0.01, 0.02, or 0.1 mg/kg) was injected subcutaneously into the ipsilateral knee area once daily for 14 days. A von Frey test was performed to assess the nociceptive response, and the altered walking parameters were evaluated using an automated gait analysis system. In addition, the peripheral and central expression changes in substance P (Sub P) were measured in the dorsal root ganglion and spinal cord by immunofluorescence. RESULTS: Repeated BV treatment at the 2 higher doses used in this study (0.02 and 0.1 mg/kg) alleviated the pain responses remarkably and recovered the gait performances to the level of acetaminophen (200 mg/kg, intraperitoneal, once daily), which used as the positive control group. Moreover, BV stimulation had an inhibitory effect on the increased expression of Sub P in the peripheral and central nervous systems by a burn injury. CONCLUSIONS: These results suggest that a peripheral BV treatment may have positive potency in treating burn-induced pain. |
format | Online Article Text |
id | pubmed-7850793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78507932021-02-08 Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice Kang, Dong-Wook Choi, Jae-Gyun Kim, Jaehyuk Park, Jin Bong Lee, Jang-Hern Kim, Hyun-Woo J Vet Sci Original Article BACKGROUND: Scalding burn injuries can occur in everyday life but occur more frequently in young children. Therefore, it is important to develop more effective burn treatments. OBJECTIVES: This study examined the effects of bee venom (BV) stimulation on scalding burn injury-induced nociception in mice as a new treatment for burn pain. METHODS: To develop a burn injury model, the right hind paw was immersed temporarily in hot water (65°C, 3 seconds). Immediately after the burn, BV (0.01, 0.02, or 0.1 mg/kg) was injected subcutaneously into the ipsilateral knee area once daily for 14 days. A von Frey test was performed to assess the nociceptive response, and the altered walking parameters were evaluated using an automated gait analysis system. In addition, the peripheral and central expression changes in substance P (Sub P) were measured in the dorsal root ganglion and spinal cord by immunofluorescence. RESULTS: Repeated BV treatment at the 2 higher doses used in this study (0.02 and 0.1 mg/kg) alleviated the pain responses remarkably and recovered the gait performances to the level of acetaminophen (200 mg/kg, intraperitoneal, once daily), which used as the positive control group. Moreover, BV stimulation had an inhibitory effect on the increased expression of Sub P in the peripheral and central nervous systems by a burn injury. CONCLUSIONS: These results suggest that a peripheral BV treatment may have positive potency in treating burn-induced pain. The Korean Society of Veterinary Science 2021-01 2021-01-15 /pmc/articles/PMC7850793/ /pubmed/33522161 http://dx.doi.org/10.4142/jvs.2021.22.e9 Text en © 2021 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://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 | Original Article Kang, Dong-Wook Choi, Jae-Gyun Kim, Jaehyuk Park, Jin Bong Lee, Jang-Hern Kim, Hyun-Woo Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title | Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title_full | Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title_fullStr | Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title_full_unstemmed | Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title_short | Bee venom reduces burn-induced pain via the suppression of peripheral and central substance P expression in mice |
title_sort | bee venom reduces burn-induced pain via the suppression of peripheral and central substance p expression in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7850793/ https://www.ncbi.nlm.nih.gov/pubmed/33522161 http://dx.doi.org/10.4142/jvs.2021.22.e9 |
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