Department of OrthopaedicsThe Graduate School, Tianjin Medical University, Tianjin, China.
Hebei Key Laboratory of Integrated Traditional and Western Medicine in Osteoarthrosis Research (Preparing), Cangzhou, China.
J Orthop Surg Res. 2023 Jun 9;18(1):419. doi: 10.1186/s13018-023-03902-6.
Spinal cord injury (SCI), which reportedly induces severe motor dysfunction, imposes a significant social and financial burden on affected individuals, families, communities, and nations. Acupuncture combined with moxibustion (AM) therapy has been widely used for motor dysfunction treatment, but the underlying mechanisms remain unknown. In this work, we aimed to determine whether AM therapy could alleviate motor impairment post-SCI and, if so, the potential mechanism.
A SCI model was established in mice through impact methods. AM treatment was performed in SCI model mice at Dazhui (GV14) and Jiaji points (T7-T12), Mingmen (GV4), Zusanli (ST36), and Ciliao (BL32) on both sides for 30 min once per day for 28 days. The Basso-Beattie-Bresnahan score was used to assess motor function in mice. A series of experiments including astrocytes activation detected by immunofluorescence, the roles of NOD-like receptor pyrin domain-containing-3 (NLRP3)-IL-18 signaling pathway with the application of astrocyte-specific NLRP3 knockout mice, and western blot were performed to explore the specific mechanism of AM treatment in SCI.
Our data indicated that mice with SCI exposure exhibited motor dysfunction, a significant decrease of neuronal cells, a remarkable activation of astrocytes and microglia, an increase of IL-6, TNF-α, IL-18 expression, and an elevation of IL-18 colocalized with astrocytes, while astrocytes-specific NLRP3 knockout heavily reversed these changes. Besides, AM treatment simulated the neuroprotective effects of astrocyte-specific NLRP3 knockout, whereas an activator of NLRP3 nigericin partially reversed the AM neuroprotective effects.
AM treatment mitigates SCI-induced motor dysfunction in mice; this protective mechanism may be related to the NLRP3-IL18 signaling pathway inhibition in astrocytes.
脊髓损伤(SCI)可导致严重的运动功能障碍,给患者、家庭、社区和国家带来巨大的社会和经济负担。针灸联合艾灸(AM)疗法已广泛用于运动功能障碍的治疗,但作用机制尚不清楚。本研究旨在探讨 AM 疗法是否能缓解 SCI 后的运动功能障碍,如果能,其潜在机制是什么。
采用重物打击法建立 SCI 模型,对 SCI 模型小鼠双侧大椎(GV14)和夹脊穴(T7-T12)、命门(GV4)、足三里(ST36)、次髎(BL32)进行 AM 治疗,每天 1 次,每次 30 min,共 28 天。采用 Basso-Beattie-Bresnahan 评分评估小鼠的运动功能。通过免疫荧光检测星形胶质细胞的激活,利用星形胶质细胞特异性 NLRP3 敲除小鼠,进行一系列实验,包括 NLRP3-IL18 信号通路的作用,以及 Western blot 检测,探讨 AM 治疗 SCI 的具体机制。
SCI 暴露的小鼠出现运动功能障碍,神经元细胞明显减少,星形胶质细胞和小胶质细胞显著激活,IL-6、TNF-α、IL-18 表达增加,IL-18 与星形胶质细胞共定位增加,而星形胶质细胞特异性 NLRP3 敲除小鼠则明显逆转了这些变化。此外,AM 治疗模拟了星形胶质细胞特异性 NLRP3 敲除的神经保护作用,而 NLRP3 的激动剂 Nigericin 则部分逆转了 AM 的神经保护作用。
AM 治疗可减轻 SCI 诱导的小鼠运动功能障碍;这种保护机制可能与星形胶质细胞中 NLRP3-IL18 信号通路的抑制有关。