King's Lab, Shanghai Jiao Tong University School of Pharmacy, Shanghai, 200240, China.
King's Lab, Shanghai Jiao Tong University School of Pharmacy, Shanghai, 200240, China.
Biomed Pharmacother. 2020 May;125:109898. doi: 10.1016/j.biopha.2020.109898. Epub 2020 Jan 29.
Electroacupuncture produces analgesia in chronic pain patients and animal models of pain hypersensitivity. The current study aims to illustrate the mechanisms underlying electroacupuncture-attenuated neuropathic pain. Neuropathic rats, induced by tight ligation of L5/L6 spinal nerves, markedly reduced mechanical thresholds in the ipsilateral hindpaws relative to the contralateral hindpaws. Low frequency (2 Hz) electroacupuncture stimulation for a period of 20 min alleviated neuropathic pain in the ipsilateral hindpaws of neuropathic rats in a time-dependent manner. The same electroacupuncture treatment also stimulated spinal gene and protein expression of IL-10 and β-endorphin but not dynorphin A, measured by real-time quantitative PCR and ELISA kits. Intrathecal injection of the specific IL-10 antibody in neuropathic rats completely blocked electroacupuncture-increased spinal expression of β-endorphin, but the β-endorphin antibody failed to alter electroacupuncture-stimulated spinal IL-10 expression. Using a double fluorescence immunostaining technique, we observed that electroacupuncture stimulated spinal IL-10 and β-endorphin expression in microglia but not in neurons or astrocytes in the spinal dorsal horn of neuropathic rats. Pretreatment with intrathecal injection of the microglial inhibitor minocycline, specific IL-10 antibody and β-endorphin antiserum (but not the dynorphin A antibody), or selective μ-opioid receptor antagonist CTAP (but not κ- or δ-opioid receptor antagonist) completely blocked electroacupuncture-induced attenuation of neuropathic pain. These results suggest that low frequency electroacupuncture alleviates neuropathic pain through stimulation of the spinal microglial expression of IL-10 and subsequent expression of β-endorphin.
电针对慢性疼痛患者和疼痛超敏反应的动物模型具有镇痛作用。本研究旨在阐明电针减轻神经性疼痛的机制。通过对 L5/L6 脊神经的紧密结扎,诱导出神经性疼痛的大鼠,其同侧后足的机械阈值明显低于对侧后足。低频(2 Hz)电针刺激 20 分钟,以时间依赖性方式减轻神经性疼痛大鼠同侧后足的神经性疼痛。同样的电针治疗还刺激了脊髓中 IL-10 和 β-内啡肽的基因和蛋白表达,但 dynorphin A 则没有,这是通过实时定量 PCR 和 ELISA 试剂盒测量的。在神经性疼痛大鼠中鞘内注射特异性 IL-10 抗体可完全阻断电针增加的脊髓 β-内啡肽表达,但 β-内啡肽抗体未能改变电针刺激的脊髓 IL-10 表达。使用双荧光免疫染色技术,我们观察到电针刺激了神经性疼痛大鼠脊髓背角中微胶质细胞的 IL-10 和 β-内啡肽表达,但没有刺激神经元或星形胶质细胞。鞘内注射微胶质细胞抑制剂米诺环素、特异性 IL-10 抗体和 β-内啡肽抗血清(但不是 dynorphin A 抗体),或选择性 μ-阿片受体拮抗剂 CTAP(但不是 κ-或 δ-阿片受体拮抗剂)预处理,可完全阻断电针引起的神经性疼痛缓解。这些结果表明,低频电针通过刺激脊髓小胶质细胞中 IL-10 的表达和随后的 β-内啡肽表达来缓解神经性疼痛。