Department of Integrative Medicine and Neurobiology, Institutes of Integrative Medicine School of Basic Medical Sciences, Institutes of Brain Science, Brain Science Collaborative Innovation Center, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Fudan University Shanghai, P. R. China.
Am J Chin Med. 2020;48(4):793-811. doi: 10.1142/S0192415X20500408. Epub 2020 May 15.
Acupuncture reduces pain by activating specific areas called acupoints on the patient's body. When these acupoints are fully activated, sensations of soreness, numbness, fullness, or heaviness called De qi or Te qi are felt by clinicians and patients. There are two kinds of acupuncture, manual acupuncture and electroacupuncture (EA). Compared with non-acupoints, acupoints are easily activated on the basis of their special composition of blood vessels, mast cells, and nerve fibers that mediate the acupuncture signals. In the spinal cord, EA can inhibit glial cell activation by down-regulating the chemokine CX3CL1 and increasing the anti-inflammatory cytokine interleukin-10. This inhibits P38 mitogen-activated protein kinase and extracellular signal-regulated kinase pathways, which are associated with microglial activation of the C-Jun N-terminal kinase signaling pathway and subsequent astrocyte activation. The inactivation of spinal microglia and astrocytes mediates the immediate and long-term analgesic effects of EA, respectively. A variety of pain-related substances released by glial cells such as the proinflammatory cytokines tumor necrosis factor [Formula: see text], interleukin-1[Formula: see text], interleukin-6, and prostaglandins such as prostaglandins E2 can also be reduced. The descending pain modulation system in the brain, including the anterior cingulated cortex, the periaqueductal gray, and the rostral ventromedial medulla, plays an important role in EA analgesia. Multiple transmitters and modulators, including endogenous opioids, cholecystokinin octapeptide, 5-hydroxytryptamine, glutamate, noradrenalin, dopamine, [Formula: see text]-aminobutyric acid, acetylcholine, and orexin A, are involved in acupuncture analgesia. Finally, the "Acupuncture [Formula: see text]" strategy is introduced to help clinicians achieve better analgesic effects, and a newly reported acupuncture method called acupoint catgut embedding, which injects sutures made of absorbable materials at acupoints to achieve long-term effects, is discussed.
针刺通过激活患者身体上的特定穴位来减轻疼痛。当这些穴位被充分激活时,临床医生和患者会感觉到酸痛、麻木、饱满或沉重等感觉,称为得气或真气。针刺有两种,即手动针刺和电针(EA)。与非穴位相比,穴位在其特殊的血管、肥大细胞和神经纤维组成的基础上更容易被激活,这些结构介导针刺信号。在脊髓中,EA 通过下调趋化因子 CX3CL1 和增加抗炎细胞因子白细胞介素-10 来抑制神经胶质细胞的激活。这抑制了丝裂原活化蛋白激酶 P38 和细胞外信号调节激酶途径,这些途径与小胶质细胞中 c-Jun N 端激酶信号通路的激活和随后的星形胶质细胞激活有关。脊髓中小胶质细胞和星形胶质细胞的失活分别介导了 EA 的即时和长期镇痛作用。神经胶质细胞释放的多种与疼痛相关的物质,如促炎细胞因子肿瘤坏死因子 [Formula: see text]、白细胞介素-1[Formula: see text]、白细胞介素-6 和前列腺素 E2 等,也可以减少。大脑中的下行疼痛调制系统,包括前扣带皮层、导水管周围灰质和头端延髓腹内侧,在 EA 镇痛中起着重要作用。多种递质和调质,包括内源性阿片肽、胆囊收缩素八肽、5-羟色胺、谷氨酸、去甲肾上腺素、多巴胺、γ-氨基丁酸、乙酰胆碱和食欲素 A,参与了针刺镇痛。最后,介绍了“针刺[Formula: see text]”策略,以帮助临床医生达到更好的镇痛效果,并讨论了一种新报道的针刺方法,即穴位埋线,该方法在穴位注射可吸收材料缝线以达到长期效果。