• This record comes from PubMed

Silver Needle Thermal Therapy Improves Mitochondrial Injury in the Skeletal Muscle of MPS Rats by Inhibiting the TRPV1/CaMKII Pathway

. 2025 Jul 23 ; 74 (3) : 481-492.

Language English Country Czech Republic Media print

Document type Journal Article

The objective of this study is to elucidate the therapeutic mechanisms underlying silver needle thermal therapy (SNT) in alleviating skeletal muscle mitochondrial damage in a rat model of myofascial pain syndrome (MPS), with particular emphasis on its regulatory role concerning TRPV1/CaMKII. The MPS rat model was established through blunt impact and eccentric movement. Interventions included SNT and local intramuscular injections of anti-TRPV1 miRNA. Behavioral assessments were conducted to measure the mechanical and thermal pain thresholds of the rats. Histopathological staining was performed to evaluate muscle structure, while mitochondrial damage was assessed using transmission electron microscopy. Western blotting analysis was employed to quantify expression levels of TRPV1, CaMKII, and CytC. Additionally, immunofluorescence techniques were applied to analyze both the expression levels of TRPV1 and its co-localization with CaMKII. Following administration of SNT and anti-TRPV1 miRNA injections, a downregulation in the expression levels of TRPV1, CaMKII, and CytC within the muscle tissue of MPS rats was observed; concurrently, mitochondrial damage exhibited improvement. The implementation of SNT and the inhibition of TRPV1 lead to a reduction in CaMKII, thereby alleviating mitochondrial damage, indicating that TRPV1 is a potential target for silver needle thermal therapy of MPS. Key words SNT " MPS " Mitochondria " TRPV1 " CaMKII.

See more in PubMed

Borg-Stein J, Simons DG. Myofascial pain. Arch Phys Med Rehabil. 2002;83(3 Suppl 1):S40–S47. doi: 10.1053/apmr.2002.32155. PubMed DOI

Saxena A, Chansoria M, Tomar G, Kumar A. Myofascial pain syndrome: an overview. J Pain Palliat Care Pharmacother. 2015;29:16–21. doi: 10.3109/15360288.2014.997853. PubMed DOI

Wang Y, Zhang YH, Wang JY, Huang YX, Wo CX, Wang CX, Zhou PR, Wang L. Changes in skeletal muscle mitochondria and SIRT3 expression in rats with myofascial pain syndrome treated by silver needle thermal conduction. Chin J Tissue Eng Res. 2024;28:2202.

Flatters SJ. The contribution of mitochondria to sensory processing and pain. Prog Mol Biol Transl Sci. 2015;131:119–146. doi: 10.1016/bs.pmbts.2014.12.004. PubMed DOI

Joseph EK, Levine JD. Mitochondrial electron transport in models of neuropathic and inflammatory pain. Pain. 2006;121:105–114. doi: 10.1016/j.pain.2005.12.010. PubMed DOI

Brandão ML, Roselino JE, Piccinato CE, Cherri J. Mitochondrial alterations in skeletal muscle submitted to total ischemia. J Surg Res. 2003;110:235–240. doi: 10.1016/S0022-4804(02)00093-8. PubMed DOI

Romanello V, Sandri M. The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass. Cell Mol Life Sci. 2021;78:1305–1328. doi: 10.1007/s00018-020-03662-0. PubMed DOI PMC

Yi-Kai L, Xueyan A, Fu-Gen W. Silver needle therapy for intractable low-back pain at tender point after removal of nucleus pulposus. J Manipulative Physiol Ther. 2000;23:320–323. doi: 10.1067/mmt.2000.106869. PubMed DOI

Wang R, Zhi-De Y. Brief introduction to silver needle warming therapy. (Article in Chinese) Zhongguo Zhen Jiu. 2006;26:36–38. PubMed

Frias B, Merighi A. Capsaicin, nociception and pain. Molecules. 2016;21:797. doi: 10.3390/molecules21060797. PubMed DOI PMC

Caterina MJ, Schumacher MA, Tominaga M, Rosen TA, Levine JD, Julius D. The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature. 1997;389:816–824. doi: 10.1038/39807. PubMed DOI

Lotteau S, Ducreux S, Romestaing C, Legrand C, Van Coppenolle F. Characterization of functional TRPV1 channels in the sarcoplasmic reticulum of mouse skeletal muscle. PLoS One. 2013;8:e58673. doi: 10.1371/journal.pone.0058673. PubMed DOI PMC

Hsiao I-H, Lin Y-W. Electroacupuncture reduces fibromyalgia pain by attenuating the HMGB1, S100B, and TRPV1 signalling pathways in the mouse brain. Evid Based Complement Alternat Med. 2022;2022:2242074. doi: 10.1155/2022/2242074. PubMed DOI PMC

Liao H-Y, Lin M-C, Lin Y-W. Acupuncture points injection mitigates chronic pain through transient receptor potential V1 in mice. Iran J Basic Med Sci. 2022;25:451. doi: 10.22038/IJBMS.2022.60121.13327. PubMed DOI PMC

Zhang RY, Zhu BF, Zhao JG, Long Z, Wang LK. Electroacupuncture Stimulation Alleviates Inflammatory Pain in Male Rats by Suppressing Oxidative Stress. Physiol Res. 2023;72:657. doi: 10.33549/physiolres.934965. PubMed DOI PMC

Kang JH, Lee H-S, Park D, Kang Y-W, Kim SM, Gong J-R, Cho K-H. Context-independent essential regulatory interactions for apoptosis and hypertrophy in the cardiac signaling network. Sci Rep. 2017;7:34. doi: 10.1038/s41598-017-00086-y. PubMed DOI PMC

Timmins JM, Ozcan L, Seimon TA, Li G, Malagelada C, Backs J, Backs T, et al. Calcium/calmodulin-dependent protein kinase II links ER stress with Fas and mitochondrial apoptosis pathways. J Clin Invest. 2009;119:2925–2941. doi: 10.1172/JCI38857. PubMed DOI PMC

Guo S-H, Lin J-P, Huang L-E, Yang Y, Chen C-Q, Li N-N, Su M-Y, et al. Silencing of spinal Trpv1 attenuates neuropathic pain in rats by inhibiting CAMKII expression and ERK2 phosphorylation. Sci Rep. 2019;9:2769. doi: 10.1038/s41598-019-39184-4. PubMed DOI PMC

Yao MH, Huang QM. Research on experimental animal models of myofascial trigger point pain. Chin J Sports Med. 2009:415–418.

L’upták M, Hroudová J. Important role of mitochondria and the effect of mood stabilizers on mitochondrial function. Physiol Res. 2019;68(Suppl 1):S3–S15. doi: 10.33549/physiolres.934324. PubMed DOI

Bock FJ, Tait SW. Mitochondria as multifaceted regulators of cell death. Nat Rev Mol Cell Biol. 2020;21:85–100. doi: 10.1038/s41580-019-0173-8. PubMed DOI

Xin H, Tanaka H, Yamaguchi M, Takemori S, Nakamura A, Kohama K. Vanilloid receptor expressed in the sarcoplasmic reticulum of rat skeletal muscle. Biochem Biophys Res Commun. 2005;332:756–762. doi: 10.1016/j.bbrc.2005.05.016. PubMed DOI

Garami A, Pakai E, Oliveira DL, Steiner AA, Wanner SP, Almeida MC, Lesnikov VA, Gavva NR, Romanovsky AA. Thermoregulatory phenotype of the Trpv1 knockout mouse: thermoeffector dysbalance with hyperkinesis. J Neurosci. 2011;31:1721–1733. doi: 10.1523/JNEUROSCI.4671-10.2011. PubMed DOI PMC

Martinez-Canton M, Gallego-Selles A, Galvan-Alvarez V, Garcia-Gonzalez E, Garcia-Perez G, Santana A, Martin-Rincon M, Calbet JA. CaMKII protein expression and phosphorylation in human skeletal muscle by immunoblotting: Isoform specificity. Free Radic Biol Med. 2024;224:182–189. doi: 10.1016/j.freeradbiomed.2024.08.030. PubMed DOI

Fernández-Carvajal A, Fernández-Ballester G, Ferrer-Montiel A. TRPV1 in chronic pruritus and pain: Soft modulation as a therapeutic strategy. Front Mol Neurosci. 2022;15:930964. doi: 10.3389/fnmol.2022.930964. PubMed DOI PMC

Arora V, Campbell JN, Chung M-K. Fight fire with fire: Neurobiology of capsaicin-induced analgesia for chronic pain. Pharmacol Ther. 2021;220:107743. doi: 10.1016/j.pharmthera.2020.107743. PubMed DOI PMC

Touska F, Marsakova L, Teisinger J, Vlachova V. A “cute” desensitization of TRPV1. Curr Pharm Biotechnol. 2011;12:122–129. doi: 10.2174/138920111793937826. PubMed DOI

Novakova-Tousova K, Vyklicky L, Susankova K, Benedikt J, Samad A, Teisinger J, Vlachova V. Functional changes in the vanilloid receptor subtype 1 channel during and after acute desensitization. Neuroscience. 2007;149:144–154. doi: 10.1016/j.neuroscience.2007.07.039. PubMed DOI

Luo L, Wang Y, Li B, Xu L, Kamau PM, Zheng J, Yang F, Yang S, Lai R. Molecular basis for heat desensitization of TRPV1 ion channels. Nat Commun. 2019;10:2134. doi: 10.1038/s41467-019-09965-6. PubMed DOI PMC

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...