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Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice
BACKGROUND: The treatment, and efficacy thereof, is considered to be inadequate with specificity to alleviation of Fibromyalgia and its associated pain. Fibromyalgia patients suffer from chronic and persistent widespread pain and generalized tenderness. Transient receptor potential V1 (TRPV1), which...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173787/ https://www.ncbi.nlm.nih.gov/pubmed/34082798 http://dx.doi.org/10.1186/s13020-021-00451-0 |
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author | Liao, Hsien-Yin Lin, Yi-Wen |
author_facet | Liao, Hsien-Yin Lin, Yi-Wen |
author_sort | Liao, Hsien-Yin |
collection | PubMed |
description | BACKGROUND: The treatment, and efficacy thereof, is considered to be inadequate with specificity to alleviation of Fibromyalgia and its associated pain. Fibromyalgia patients suffer from chronic and persistent widespread pain and generalized tenderness. Transient receptor potential V1 (TRPV1), which is reported as a Ca(2+) permeable ion channel that can be activated by inflammation, is reported to be involved in the development of fibromyalgia pain. METHODS: The current study explored the TRPV1 channel functions as a noxious sensory input in mice cold stress model. It remains unknown whether electroacupuncture (EA) attenuates fibromyalgia pain or affects the TRPV1 pathway. RESULTS: We show that cold stress increases mechanical and thermal pain (day 7: mechanical: 1.69 ± 0.41 g; thermal: 4.68 ± 0.56 s), and that EA and Trpv1 deletion counter this increase. EA and Trpv1 deletion reduced the cold stress-induced increase in inflammatory mediators and TRPV1-related molecules in the hypothalamus, periaqueductal gray (PAG), and cerebellum of mice. CONCLUSIONS: Our results imply that EA has an analgesic effect associated with TRPV1 downregulation. We provide novel evidence that these inflammatory mediators can modulate the TRPV1 signaling pathway and suggest new potential therapeutic targets for fibromyalgia pain. |
format | Online Article Text |
id | pubmed-8173787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81737872021-06-03 Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice Liao, Hsien-Yin Lin, Yi-Wen Chin Med Research BACKGROUND: The treatment, and efficacy thereof, is considered to be inadequate with specificity to alleviation of Fibromyalgia and its associated pain. Fibromyalgia patients suffer from chronic and persistent widespread pain and generalized tenderness. Transient receptor potential V1 (TRPV1), which is reported as a Ca(2+) permeable ion channel that can be activated by inflammation, is reported to be involved in the development of fibromyalgia pain. METHODS: The current study explored the TRPV1 channel functions as a noxious sensory input in mice cold stress model. It remains unknown whether electroacupuncture (EA) attenuates fibromyalgia pain or affects the TRPV1 pathway. RESULTS: We show that cold stress increases mechanical and thermal pain (day 7: mechanical: 1.69 ± 0.41 g; thermal: 4.68 ± 0.56 s), and that EA and Trpv1 deletion counter this increase. EA and Trpv1 deletion reduced the cold stress-induced increase in inflammatory mediators and TRPV1-related molecules in the hypothalamus, periaqueductal gray (PAG), and cerebellum of mice. CONCLUSIONS: Our results imply that EA has an analgesic effect associated with TRPV1 downregulation. We provide novel evidence that these inflammatory mediators can modulate the TRPV1 signaling pathway and suggest new potential therapeutic targets for fibromyalgia pain. BioMed Central 2021-06-03 /pmc/articles/PMC8173787/ /pubmed/34082798 http://dx.doi.org/10.1186/s13020-021-00451-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liao, Hsien-Yin Lin, Yi-Wen Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title | Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title_full | Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title_fullStr | Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title_full_unstemmed | Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title_short | Electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential V1 in mice |
title_sort | electroacupuncture reduces cold stress-induced pain through microglial inactivation and transient receptor potential v1 in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8173787/ https://www.ncbi.nlm.nih.gov/pubmed/34082798 http://dx.doi.org/10.1186/s13020-021-00451-0 |
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