Department of Spine Surgery, Inner Mongolia People's Hospital, Hohhot, Inner Mongolia, China.
Department of Orthopedics and Traumatology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan China.
Immunol Invest. 2023 Nov;52(4):399-414. doi: 10.1080/08820139.2023.2183135. Epub 2023 Mar 28.
Zhenbao Pill contains many Chinese herbal medicinal ingredients and has been proven to have therapeutic effects on the repair of spinal cord injury (SCI). This study attempts to investigate the role of formononetin (FMN), an ingredient of Zhenbao Pill, in regulating neuroinflammation after SCI and the underlying mechanism. Primary microglia isolated from the spinal cord of newborn rats and human microglial clone 3 (HMC3) cells were stimulated with IL-1β followed by FMN incubation. The cell viability and inflammatory cytokine levels were detected. The target of FMN was predicted and screened using databases. By silencing or overexpression of epidermal growth factor receptor (EGFR), the anti-neuroinflammatory effect of FMN was assessed in vitro. In vivo, FMN was intraperitoneally injected into rats after SCI followed by the neurological function and histopathology examination. The isolated microglia were in high purity, and the different concentrations of FMN incubation had no toxic effects on primary microglia and HMC3 cells. FMN reduced the inflammatory cytokine levels (TNF-α and IL-6) in a concentration-dependent manner. EGFR silencing or FMN incubation decreased p-EGFR and p-p38 levels and down-regulated inflammatory cytokine levels in IL-1β-stimulated cells or supernatants. Nevertheless, the effects of FMN on microglial inflammation were reversed by EGFR overexpression. In vivo, FMN treatment improved the neuromotor function, repaired tissue injury, and inhibited EGFR/p38MAPK phosphorylation. Formononetin inhibits microglial inflammatory response and contributes to SCI repair via the EGFR/p38MAPK signaling pathway.
振宝丸含有多种中药成分,已被证明对脊髓损伤(SCI)的修复具有治疗作用。本研究试图探讨振宝丸的有效成分芒柄花素(FMN)在调节 SCI 后神经炎症中的作用及其机制。用白细胞介素-1β(IL-1β)刺激新生大鼠脊髓原代小胶质细胞和人小胶质细胞克隆 3(HMC3)细胞,然后用 FMN 孵育。检测细胞活力和炎症细胞因子水平。利用数据库预测和筛选 FMN 的作用靶点。通过沉默或过表达表皮生长因子受体(EGFR),评估 FMN 在体外的抗炎作用。在体内,SCI 后给大鼠腹腔内注射 FMN,然后进行神经功能和组织病理学检查。分离的小胶质细胞纯度高,不同浓度的 FMN 孵育对原代小胶质细胞和 HMC3 细胞没有毒性作用。FMN 呈浓度依赖性降低炎症细胞因子(TNF-α和 IL-6)水平。沉默 EGFR 或用 FMN 孵育可降低 IL-1β刺激的细胞或上清液中 p-EGFR 和 p-p38MAPK 水平,并下调炎症细胞因子水平。然而,EGFR 过表达逆转了 FMN 对小胶质细胞炎症的作用。在体内,FMN 治疗可改善运动功能,修复组织损伤,并抑制 EGFR/p38MAPK 磷酸化。芒柄花素通过 EGFR/p38MAPK 信号通路抑制小胶质细胞炎症反应,促进 SCI 修复。