Yao Kaifang, Chen Zhihan, Li Yanwei, Dou Baomin, Xu Zhifang, Ma Yajing, Du Simin, Wang Jiangshan, Fu Jiangjiang, Liu Qi, Fan Zezhi, Liu Yangyang, Lin Xiaowei, Xu Yuan, Fang Yuxin, Wang Shenjun, Guo Yi
Research Center of Experimental Acupuncture Science, Tianjin University of Traditional Chinese Medicine, Tianjin City, People's Republic of China.
School of Acupuncture & Moxibustion and Tuina, Tianjin University of Traditional Chinese Medicine, Tianjin City, People's Republic of China.
J Inflamm Res. 2024 Mar 20;17:1823-1837. doi: 10.2147/JIR.S455699. eCollection 2024.
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.
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.
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.
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.
针刺已被证明可减轻炎性疼痛。机械感受器存在于穴位中。当针刺施加机械力时,这些离子通道打开并将机械信号转化为生化信号。瞬时受体电位锚蛋白1(TRPA1)能够感知各种物理和化学刺激,并作为炎症和疼痛的传感器。这种蛋白质在免疫细胞中表达,并在早期组织损伤和炎症期间有助于局部防御机制。在本研究中,我们调查了TRPA1在针刺镇痛中的作用。
我们将完全弗氏佐剂(CFA)注射到小鼠足底以建立痛觉过敏模型。进行免疫组织化学和免疫荧光分析以确定针刺对足三里(ST36)中TRPA1表达的影响。我们使用TRPA1基因敲除小鼠和药理学方法拮抗TRPA1以观察对针刺镇痛的影响。在此基础上,使用胶原酶破坏ST36处的胶原纤维以观察对TRPA1的影响。
我们发现,与CFA组相比,针刺组ST36处TRPA1阳性肥大细胞、巨噬细胞和成纤维细胞的数量显著增加。在CFA诱导的炎性疼痛模型中,与TRPA1基因敲除针刺组相比,针刺组的爪退缩潜伏期(PWL)和爪退缩阈值(PWT)显著下调。在针刺+高、中、低剂量HC-030031组与针刺组相比,PWL和PWT下调,并且在角叉菜胶诱导的炎性疼痛模型中结果与此一致。我们进一步发现,与针刺组相比,针刺+胶原酶组ST36处TRPA1阳性肥大细胞、巨噬细胞和成纤维细胞的数量下调。
这些发现共同表明,TRPA1在ST36针刺产生的镇痛作用中起重要作用。这为针刺治疗疼痛性疾病提供了新的证据。