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炙乌头碱通过抑制 JAK2/STAT3 信号通路缓解重症肌无力:在小鼠模型中的研究。

Grilled nux vomica alleviates myasthenia gravis by inhibiting the JAK2/STAT3 signaling pathway: a study in a mice model.

机构信息

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.

出版信息

Eur J Med Res. 2024 Oct 21;29(1):507. doi: 10.1186/s40001-024-02100-2.

Abstract

BACKGROUND

Grilled Nux Vomica (GNV) is a promising traditional Chinese medicine to treat myasthenia gravis (MG), but its effects and mechanisms need further exploration.

METHODS

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.

RESULTS

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.

CONCLUSIONS

GNV improves MG by inhibiting the JAK2/STAT3 pathway, which might be an effective therapeutic strategy for MG.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eab/11492534/31749e99ed9a/40001_2024_2100_Fig1_HTML.jpg

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