AI Article Synopsis

  • Acupuncture has been shown to reduce inflammatory pain by activating mechanoreceptors in specific acupuncture points, which can influence the TRPA1 protein, a key player in sensing pain and inflammation.
  • In experiments using mice, researchers used various methods to study how acupuncture affects TRPA1 expression and its role in pain relief, particularly at the Zusanli (ST36) point.
  • Results indicated that acupuncture not only increased the presence of TRPA1-positive immune cells but also effectively reduced pain thresholds, suggesting that TRPA1 is crucial for the analgesic effects of acupuncture.*

Article Abstract

Purpose: Acupuncture (ACU) has been demonstrated to alleviate inflammatory pain. Mechanoreceptors are present in acupuncture points. When acupuncture exerts mechanical force, these ion channels open and convert the mechanical signals into biochemical signals. TRPA1 (T ransient receptor potential ankyrin 1) is capable of sensing various physical and chemical stimuli and serves as a sensor for inflammation and pain. This protein is expressed in immune cells and contributes to local defense mechanisms during early tissue damage and inflammation. In this study, we investigated the role of TRPA1 in acupuncture analgesia.

Patients And Methods: We injected complete Freund's adjuvant (CFA) into the mouse plantars to establish a hyperalgesia model. Immunohistochemistry and immunofluorescence analyses were performed to determine the effect of acupuncture on the TRPA1 expression in the Zusanli (ST36). We used TRPA1 mouse and pharmacological methods to antagonize TRPA1 to observe the effect on acupuncture analgesia. On this basis, collagenase was used to destroy collagen fibers at ST36 to observe the effect on TRPA1.

Results: We found that the ACU group vs the CFA group, the number of TRPA1-positive mast cells, macrophages, and fibroblasts at the ST36 increased significantly. In CFA- inflammatory pain models, the TRPA1 ACU vs TRPA1 ACU groups, the paw withdrawal latency (PWL) and paw withdrawal threshold (PWT) downregulated significantly. In the ACU + high-, ACU + medium-, ACU + low-dose HC-030031 vs ACU groups, the PWL and PWT were downregulated, and in carrageenan-induced inflammatory pain models were consistent with these results. We further found the ACU + collagenase vs ACU groups, the numbers of TRPA1-positive mast cells, macrophages, and fibroblasts at the ST36 were downregulated.

Conclusion: These findings together imply that TRPA1 plays a significant role in the analgesic effects produced via acupuncture at the ST36. This provides new evidence for acupuncture treatment of painful diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10961083PMC
http://dx.doi.org/10.2147/JIR.S455699DOI Listing

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