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Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection
BACKGROUND: Fibromyalgia (FM) is a syndrome involving chronic pain, fatigue, sleep difficulties, morning stiffness and muscle cramping lasting longer than 3 months. The epidemiological prevalence is approximately 3–5% in women and increases with age. Antagonism of acid-sensing ion channel 3 (ASIC3)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278366/ https://www.ncbi.nlm.nih.gov/pubmed/31986902 http://dx.doi.org/10.1136/acupmed-2017-011457 |
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author | Yen, Liang-Ta Hsieh, Ching-Liang Hsu, Hsin-Cheng Lin, Yi-Wen |
author_facet | Yen, Liang-Ta Hsieh, Ching-Liang Hsu, Hsin-Cheng Lin, Yi-Wen |
author_sort | Yen, Liang-Ta |
collection | PubMed |
description | BACKGROUND: Fibromyalgia (FM) is a syndrome involving chronic pain, fatigue, sleep difficulties, morning stiffness and muscle cramping lasting longer than 3 months. The epidemiological prevalence is approximately 3–5% in women and increases with age. Antagonism of acid-sensing ion channel 3 (ASIC3) reportedly attenuates acid saline-induced FM pain in mice. AIMS: Whether pre-treatment with electroacupuncture (EA) or APETx2 can attenuate mechanical hyperalgesia in this murine model remains unknown. METHODS: Accordingly, we examined the analgesic effect of EA in a murine model of FM pain induced by dual injections of acid saline and investigated whether EA or APETx2 can attenuate FM pain via the ASIC3 channel. RESULTS: EA significantly reduced mechanical hyperalgesia in this model. ASIC3 antagonism, induced by injecting APETx2, also significantly reduced mechanical hyperalgesia. The expression of ASIC3 in the dorsal root ganglia, spinal cord and thalamus was increased after FM model induction. Over-expression of these nociceptive channels was attenuated by pre-treatment with EA or an ASIC3 antagonist. CONCLUSION: Our data reveal that both EA and ASIC3 blockade significantly reduce FM pain in mice via the ASIC3, Nav1.7 and Nav1.8 signalling pathways. Moreover, our findings support the potential clinical use of EA for the treatment of FM pain. |
format | Online Article Text |
id | pubmed-7278366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72783662020-06-29 Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection Yen, Liang-Ta Hsieh, Ching-Liang Hsu, Hsin-Cheng Lin, Yi-Wen Acupunct Med Original Papers BACKGROUND: Fibromyalgia (FM) is a syndrome involving chronic pain, fatigue, sleep difficulties, morning stiffness and muscle cramping lasting longer than 3 months. The epidemiological prevalence is approximately 3–5% in women and increases with age. Antagonism of acid-sensing ion channel 3 (ASIC3) reportedly attenuates acid saline-induced FM pain in mice. AIMS: Whether pre-treatment with electroacupuncture (EA) or APETx2 can attenuate mechanical hyperalgesia in this murine model remains unknown. METHODS: Accordingly, we examined the analgesic effect of EA in a murine model of FM pain induced by dual injections of acid saline and investigated whether EA or APETx2 can attenuate FM pain via the ASIC3 channel. RESULTS: EA significantly reduced mechanical hyperalgesia in this model. ASIC3 antagonism, induced by injecting APETx2, also significantly reduced mechanical hyperalgesia. The expression of ASIC3 in the dorsal root ganglia, spinal cord and thalamus was increased after FM model induction. Over-expression of these nociceptive channels was attenuated by pre-treatment with EA or an ASIC3 antagonist. CONCLUSION: Our data reveal that both EA and ASIC3 blockade significantly reduce FM pain in mice via the ASIC3, Nav1.7 and Nav1.8 signalling pathways. Moreover, our findings support the potential clinical use of EA for the treatment of FM pain. SAGE Publications 2020-01-28 2020-06 /pmc/articles/PMC7278366/ /pubmed/31986902 http://dx.doi.org/10.1136/acupmed-2017-011457 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Papers Yen, Liang-Ta Hsieh, Ching-Liang Hsu, Hsin-Cheng Lin, Yi-Wen Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title | Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title_full | Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title_fullStr | Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title_full_unstemmed | Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title_short | Preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or APETx2 injection |
title_sort | preventing the induction of acid saline-induced fibromyalgia pain in mice by electroacupuncture or apetx2 injection |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278366/ https://www.ncbi.nlm.nih.gov/pubmed/31986902 http://dx.doi.org/10.1136/acupmed-2017-011457 |
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