Locus Coeruleus Noradrenergic-Spinal Projections Contribute to Electroacupuncture-Mediated Antinociception in Postoperative Pain in Mice

IF 14.3 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Wen-Guang Chu, Ru Zhang, Hai-Tao Li, Ying-Chun Li, Hui Ding, Zhen-Zhen Li, Wen-Juan Han, Fei Wang, Xing-Xing Zheng, Hong-Hui Mao, Hua Yuan, Sheng-Xi Wu, Rou-Gang Xie, Ceng Luo
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Abstract

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 α2A-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 α2A-adrenoceptor–CaMKII signaling cascades in the SDH contribute to EA-induced antinociception in postoperative pain.

Abstract Image

蓝斑去肾上腺素能-脊柱投射有助于电针介导的小鼠术后疼痛的抗痛觉。
术后疼痛仍然是医疗保健中的一个重大挑战。电针(EA)在帮助控制手术疼痛方面已经获得了极性,并在增强术后镇痛,减少阿片类药物需求方面显示出有益的效果。尽管如此,人们对这些行为背后的确切机制知之甚少。有证据表明去甲肾上腺素(NE)参与EA的作用。然而,EA治疗后NE的确切来源、作用机制以及疼痛调节通路中的电路位点仍不清楚。足底切开(PI)导致蓝斑(LC)去甲肾上腺素能神经元活性降低,从而导致脊髓背角(SDH) NE释放受损。EA治疗使PI后LC去肾上腺素能神经元的异常低兴奋性正常化,从而引发SDH中NE释放增强。光遗传抑制LC去肾上腺素能神经元消除PI后ea诱导的NE释放和抗伤害感受作用,而激活这些神经元模拟ea诱导的NE释放和抗伤害感受作用。EA激活脊髓α 2a -肾上腺素能受体,抑制CaMKII信号,从而增加NE释放,从而抑制脊髓兴奋性神经元的高兴奋性,最终缓解术后疼痛。由此可见,LC去甲肾上腺素能-脊柱投射和随后的SDH α 2a -肾上腺素受体- camkii信号级联有助于ea诱导的术后疼痛抗痛反应。
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来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
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