Wang Mengke, Cai Xia, Wang Yueying, Li Shizhen, Wang Na, Sun Rui, Xing Jingming, Liang Shangdong, Liu Shuangmei
Department of Physiology, Medical School of Nanchang University, Nanchang, China.
Department of Endocrinology, Second Affiliated Hospital of Nanchang University, Nanchang, China.
Front Neurosci. 2021 Jan 11;14:570831. doi: 10.3389/fnins.2020.570831. eCollection 2020.
Neurologic damage often leads to neuropathic pain, for which there are no effective treatments owing to its complex pathogenesis. The purinergic receptor P2X4 is closely associated with neuropathic pain. Astragalin (AST), a compound that is used in traditional Chinese medicine, has protective effects against allergic dermatitis and neuronal injury, but its mechanism of action is not well understood. The present study investigated whether AST can alleviate neuropathic pain in a rat model established by chronic constriction injury (CCI) to the sciatic nerve. The model rats exhibited pain behavior and showed increased expression of P2X4 and the activated satellite glial cell (SGC) marker glial fibrillary acidic protein in dorsal root ganglia (DRG). AST treatment partly abrogated the upregulation of P2X4, inhibited SGC activation, and alleviated pain behavior in CCI rats; it also suppressed ATP-activated currents in HEK293 cells overexpressing P2X4. These data demonstrate that AST relieves neuropathic pain by inhibiting P2X4 and SGC activation in DRG, highlighting its therapeutic potential for clinical pain management.
神经损伤常导致神经性疼痛,由于其发病机制复杂,目前尚无有效的治疗方法。嘌呤能受体P2X4与神经性疼痛密切相关。黄芪甲苷(AST)是一种用于中药的化合物,对过敏性皮炎和神经元损伤具有保护作用,但其作用机制尚不清楚。本研究调查了AST是否能减轻坐骨神经慢性压迫损伤(CCI)建立的大鼠模型中的神经性疼痛。模型大鼠表现出疼痛行为,背根神经节(DRG)中P2X4的表达增加,卫星胶质细胞(SGC)标记物胶质纤维酸性蛋白激活。AST治疗部分消除了P2X4的上调,抑制了SGC激活,并减轻了CCI大鼠的疼痛行为;它还抑制了过表达P2X4的HEK293细胞中的ATP激活电流。这些数据表明,AST通过抑制DRG中的P2X4和SGC激活来缓解神经性疼痛,突出了其在临床疼痛管理中的治疗潜力。