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DOI 10.22038/ijbms.2019.35887.8547

Медицинская библиотека · Iranian journal of basic medical sciences · 2019

Electroacupuncture attenuates chronic fibromyalgia pain through the phosphorylated phosphoinositide 3-kinase signaling pathway in the mouse brain.

Chen Chao-Tsung, Lin Jaung-Geng, Huang Chun-Ping, Lin Yi-Wen

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Аннотация

OBJECTIVES

Fibromyalgia (FM) is a central nervous system disorder characterized by widespread mechanical hyperalgesia due to unknown mechanisms. Several inflammatory mediators, such as interleukin-1 (IL-1), IL-6, IL-8, and tumor necrosis factor, are increased in the serum of FM patients. Although medications including pregabalin, duloxetine, and milnacipran are used to treat FM, the results are unsatisfying. In the present study we assessed whether electroacupuncture (EA) can reduce chronic FM pain and then proposed an underlying mechanism for this effect.

MATERIALS AND

METHODS

Chronic FM pain was induced in mice by dual acid saline injection lasting up to 4 weeks.

RESULTS

Chronic FM pain was treated by EA manipulation, but not in the sham operated group. Phosphorylated phosphatidylinositol 3-kinase (pPI3K), protein kinase B, mechanistic target of rapamycin, and nuclear factor kappa-light-chain-enhancer of activated B cells were unaltered in the mouse dorsal root ganglion (DRG) and spinal cord (SC) after inducing FM and administering EA treatment. The pPI3K-associated nociceptive signaling pathway was increased in the thalamus of FM mice, but reversed by EA. Similar results were observed in the mouse somatosensory cortex.

CONCLUSION

These data suggest that EA has a significant effect on a signaling pathway in brain areas of FM mice. These findings suggest the value of EA for clinical practice.

Для цитирования: Chen Chao-Tsung, Lin Jaung-Geng, Huang Chun-Ping, Lin Yi-Wen. Electroacupuncture attenuates chronic fibromyalgia pain through the phosphorylated phosphoinositide 3-kinase signaling pathway in the mouse brain.. Iranian journal of basic medical sciences. 2019. DOI: 10.22038/ijbms.2019.35887.8547.
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