Chu Wen-Guang, Zhang Ru, Li Hai-Tao, Li Ying-Chun, Ding Hui, Li Zhen-Zhen, Han Wen-Juan, Wang Fei, Zheng Xing-Xing, Mao Hong-Hui, Yuan Hua, Wu Sheng-Xi, Xie Rou-Gang, Luo Ceng
Department of Neurobiology, School of Basic Medicine, Fourth Military Medical University, Xi'an, 710032, China.
Department of Anesthesiology, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710016, China.
Adv Sci (Weinh). 2025 Jul;12(25):e01182. doi: 10.1002/advs.202501182. Epub 2025 May 19.
Postoperative pain remains a significant challenge in healthcare. Electroacupuncture (EA) has gained polarity in helping manage surgical pain and showed beneficial effects on enhancing postoperative analgesia, decreasing opioid requirement. Despite this, the precise mechanisms underlying these actions are poorly understood. Evidence shows the involvement of noradrenaline (NE) in the action of EA. However, the precise identity of the NE source after EA treatment, its mechanisms of action, and the circuitry locus in the pain-regulating pathway remain elusive. It is shown that plantar incision (PI) leads to hypoactivity of noradrenergic neurons in the locus coeruleus (LC), which brings about impaired NE release in the spinal dorsal horn (SDH). EA treatment normalizes the abnormal hypoexcitability of LC noradrenergic neurons after PI and thus triggers enhanced NE release in the SDH. Optogenetic inhibition of LC noradrenergic neurons eliminates EA-induced NE release and antinociceptive effects after PI, while activation of these neurons mimics EA-induced NE release and antinociception. The resultant increased NE release after EA activates spinal α-adrenoceptor and inhibits CaMKII signaling, which in turn depresses spinal excitatory neuronal hyperexcitability and eventually relieves postoperative pain. It is concluded that LC noradrenergic-spinal projections and subsequent α-adrenoceptor-CaMKII signaling cascades in the SDH contribute to EA-induced antinociception in postoperative pain.
术后疼痛仍然是医疗保健领域的一项重大挑战。电针(EA)在帮助管理手术疼痛方面已获得认可,并在增强术后镇痛、减少阿片类药物需求方面显示出有益效果。尽管如此,这些作用背后的确切机制仍知之甚少。有证据表明去甲肾上腺素(NE)参与了电针的作用。然而,电针治疗后NE来源的确切身份、其作用机制以及疼痛调节通路中的神经回路位点仍然难以捉摸。研究表明,足底切口(PI)导致蓝斑核(LC)中去甲肾上腺素能神经元活动减退,进而导致脊髓背角(SDH)中NE释放受损。电针治疗可使PI后LC去甲肾上腺素能神经元异常的低兴奋性恢复正常,从而触发SDH中NE释放增加。对LC去甲肾上腺素能神经元进行光遗传学抑制可消除电针诱导的PI后NE释放和抗伤害感受作用,而激活这些神经元则可模拟电针诱导的NE释放和抗伤害感受作用。电针后NE释放增加激活脊髓α-肾上腺素能受体并抑制CaMKII信号传导,进而抑制脊髓兴奋性神经元的过度兴奋,最终缓解术后疼痛。得出的结论是,LC去甲肾上腺素能-脊髓投射以及随后SDH中的α-肾上腺素能受体-CaMKII信号级联反应有助于电针在术后疼痛中诱导的抗伤害感受作用。