Department of Neurology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), No.54 Youdian Road, Hangzhou, 310006, Zhejiang Province, China.
Eur J Med Res. 2024 Oct 21;29(1):507. doi: 10.1186/s40001-024-02100-2.
Grilled Nux Vomica (GNV) is a promising traditional Chinese medicine to treat myasthenia gravis (MG), but its effects and mechanisms need further exploration.
Experimental autoimmune MG (EAMG) model was established by muscle-specific kinase (MuSK) induction on C57BL/6 J mice. Mice were treated with GNV and/or ruxolitinib (JAK2 inhibitor) or AG490 (STAT3 inhibitor) for 30 days via gavage after modeling and randomized into 7 groups: control, model, low-dose GNV, middle-dose GNV, high-dose GNV, GNV + ruxolitinib, GNV + AG490. Body weight, muscle strength, clinical score, MuSK level, neuromuscular junction integrity (agrin and acetylcholine receptor [AChR] levels), inflammatory factors (IL-2 and IL-6), and the activation of the JAK2/STAT3 pathway were measured and compared between groups.
GNV significantly improved body weight and muscle strength, as well as reduced clinical scores, MuSK levels, and inflammatory markers (IL-2 and IL-6) levels compared with untreated EAMG mice. GNV also protected the neuromuscular junction and increased agrin and AChR co-expression in a dose-dependent manner. In addition, GNV attenuated the levels of p-JAK2 and p-STAT3, which are aberrantly upregulated in EAMG mice. After co-treatment with ruxolitinib or AG490, the effect of GNV on body weight, muscle strength, clinical score, MuSK level, neuromuscular junction integrity, levels of inflammatory factors, and JAK2/STAT3 pathway was further amplified in EAMG mice.
GNV improves MG by inhibiting the JAK2/STAT3 pathway, which might be an effective therapeutic strategy for MG.
炙马钱子(GNV)是一种有前途的治疗重症肌无力(MG)的中药,但它的作用和机制需要进一步探索。
通过肌肉特异性激酶(MuSK)诱导 C57BL/6J 小鼠建立实验性自身免疫性重症肌无力(EAMG)模型。建模后,通过灌胃用 GNV 和/或鲁索替尼(JAK2 抑制剂)或 AG490(STAT3 抑制剂)处理小鼠 30 天,随机分为 7 组:对照组、模型组、低剂量 GNV 组、中剂量 GNV 组、高剂量 GNV 组、GNV+鲁索替尼组、GNV+AG490 组。比较各组间体重、肌肉力量、临床评分、MuSK 水平、神经肌肉接头完整性(神经生长因子和乙酰胆碱受体[AChR]水平)、炎症因子(IL-2 和 IL-6)和 JAK2/STAT3 通路的激活情况。
与未经治疗的 EAMG 小鼠相比,GNV 显著改善了体重和肌肉力量,降低了临床评分、MuSK 水平和炎症标志物(IL-2 和 IL-6)水平。GNV 还以剂量依赖性方式保护神经肌肉接头并增加神经生长因子和 AChR 的共表达。此外,GNV 减弱了 EAMG 小鼠中异常上调的 p-JAK2 和 p-STAT3 水平。在与鲁索替尼或 AG490 联合治疗后,GNV 对 EAMG 小鼠体重、肌肉力量、临床评分、MuSK 水平、神经肌肉接头完整性、炎症因子水平和 JAK2/STAT3 通路的作用进一步放大。
GNV 通过抑制 JAK2/STAT3 通路改善 MG,这可能是治疗 MG 的有效治疗策略。