» Articles » PMID: 32774811

Electroacupuncture Reduces Chronic Fibromyalgia Pain Through Attenuation of Transient Receptor Potential Vanilloid 1 Signaling Pathway in Mouse Brains

Overview
Specialty General Medicine
Date 2020 Aug 11
PMID 32774811
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: Fibromyalgia pain is a mysterious clinical pain syndrome, characterized by inflammation in the brain, whose molecular mechanisms are still unknown. Females are more commonly affected by fibromyalgia, exhibiting symptoms such as widespread mechanical pain, immune dysfunction, sleep disturbances, and poor quality of life. Electroacupuncture (EA) has been used to relieve several types of pain, including fibromyalgia pain.

Materials And Methods: In the present study, we used dual injections of acidic saline into the gastrocnemius muscle to initiate a neural activation that resulted in fibromyalgia pain in mice. We used the Von Frey test to measure mechanical hyperalgesia and Western blot to measure protein levels.

Results: Results indicated that mechanical hyperalgesia can be induced in mice for 4 weeks, suggesting the induction of chronic fibromyalgia (CFM). Furthermore, continuous EA treatment reliably attenuated the mechanical hyperalgesia, but not in the sham control group. Results also suggested that the mechanical hyperalgesia can be prevented in mice with TRPV1 gene deletion. Mice with CFM showed increased expressions of TRPV1, Nav1.7, and Nav1.8 in the dorsal root ganglion (DRG) and the spinal cord (SC). The expression of TRPV1-associated molecules such as pPKA, pERK, and pCREB was also increased in the thalamus and somatosensory cortex (SSC) of the mice. All the aforementioned mechanisms were reversed by EA treatment and TRPV1 gene deletion.

Conclusion: Altogether, our results implied significant mechanisms of CFM and EA-analgesia that involve the regulation of the TRPV1 signaling pathway. These findings may be relevant to the evaluation and treatment of CFM.

Citing Articles

Electroacupuncture Reduced Fibromyalgia-Pain-like Behavior through Inactivating Transient Receptor Potential V1 and Interleukin-17 in Intermittent Cold Stress Mice Model.

Yeh Y, Liao H, Hsiao I, Hsu H, Lin Y Brain Sci. 2024; 14(9).

PMID: 39335365 PMC: 11430684. DOI: 10.3390/brainsci14090869.


TRP (transient receptor potential) ion channel family: structures, biological functions and therapeutic interventions for diseases.

Zhang M, Ma Y, Ye X, Zhang N, Pan L, Wang B Signal Transduct Target Ther. 2023; 8(1):261.

PMID: 37402746 PMC: 10319900. DOI: 10.1038/s41392-023-01464-x.


Peripheral Beta-2 Adrenergic Receptors Mediate the Sympathetic Efferent Activation from Central Nervous System to Splenocytes in a Mouse Model of Fibromyalgia.

Yamashita S, Dozono N, Tobori S, Nagayasu K, Kaneko S, Shirakawa H Int J Mol Sci. 2023; 24(4).

PMID: 36834875 PMC: 9967679. DOI: 10.3390/ijms24043465.


Knowledge Mapping of Acupuncture for Fibromyalgia from 1990 to 2022: A Bibliometric Analysis.

Li P, Zheng H, Chen Y, Liu Z, He J J Pain Res. 2022; 15:2405-2426.

PMID: 36003289 PMC: 9394785. DOI: 10.2147/JPR.S379699.


Electroacupuncture Reduces Fibromyalgia Pain by Attenuating the HMGB1, S100B, and TRPV1 Signalling Pathways in the Mouse Brain.

Hsiao I, Lin Y Evid Based Complement Alternat Med. 2022; 2022:2242074.

PMID: 35341159 PMC: 8941543. DOI: 10.1155/2022/2242074.


References
1.
Strickland I, Martindale J, Woodhams P, Reeve A, Chessell I, McQueen D . Changes in the expression of NaV1.7, NaV1.8 and NaV1.9 in a distinct population of dorsal root ganglia innervating the rat knee joint in a model of chronic inflammatory joint pain. Eur J Pain. 2007; 12(5):564-72. DOI: 10.1016/j.ejpain.2007.09.001. View

2.
Lu K, Yang J, Hsieh C, Hsu Y, Lin Y . Electroacupuncture restores spatial learning and downregulates phosphorylated N-methyl-D-aspartate receptors in a mouse model of Parkinson's disease. Acupunct Med. 2016; 35(2):133-141. DOI: 10.1136/acupmed-2015-011041. View

3.
Jarvis M, Honore P, Shieh C, Chapman M, Joshi S, Zhang X . A-803467, a potent and selective Nav1.8 sodium channel blocker, attenuates neuropathic and inflammatory pain in the rat. Proc Natl Acad Sci U S A. 2007; 104(20):8520-5. PMC: 1895982. DOI: 10.1073/pnas.0611364104. View

4.
Black J, Liu S, Tanaka M, Cummins T, Waxman S . Changes in the expression of tetrodotoxin-sensitive sodium channels within dorsal root ganglia neurons in inflammatory pain. Pain. 2004; 108(3):237-247. DOI: 10.1016/j.pain.2003.12.035. View

5.
Basbaum A, Bautista D, Scherrer G, Julius D . Cellular and molecular mechanisms of pain. Cell. 2009; 139(2):267-84. PMC: 2852643. DOI: 10.1016/j.cell.2009.09.028. View