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人参皂苷Rh2通过ROS/MAPK14信号通路减轻脊髓损伤小鼠的炎症反应并促进运动功能恢复。

Ginsenoside Rh2 alleviates inflammatory response and enhances motor function recovery in spinal cord injury mice via the ROS/MAPK14 signaling pathway.

作者信息

Wu Yanlan, Song Fangming, Tan Xiuwei, Huang Jin, Lu Junliang, Yang Baihui, Fang Fang, Ye Xiaoxia, Geer Laoyi, Li Fengxin, Wei Qian, Lu Xuefeng, Xu Jiake, Jiang Jie, Su Yiji

机构信息

The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Guangxi Medical University, Nanning, China.

出版信息

J Ginseng Res. 2025 Jul;49(4):415-425. doi: 10.1016/j.jgr.2025.03.008. Epub 2025 Mar 28.

Abstract

BACKGROUND

Inhibiting inflammation in nervous system is a vital part of treating for spinal cord injury (SCI). Compounds originating from plants can decrease the damage in the spinal cord for recovering the function of nerve and interrupting the inflammatory reaction. 20(S)-Ginsenoside Rh2 (G-Rh2) from Panax ginseng is an anti-inflammatory property inhibiting the expression of MAPK14 protein by enabling the MAPK pathway. Therefore, this research explored the anti-inflammatory effects of G-Rh2 on SCI using cellular and animal models.

METHODS

To explore G-Rh2's anti-inflammatory potential in SCI, we employed bioinformatics analysis to anticipate target proteins and signaling pathways associated with G-Rh2 and SCI. We utilized BV2 microglia cells to model inflammation induced by lipopolysaccharide (LPS), and a modified Allen's technique in a mouse SCI model. Our investigation utilized a range of methodologies including quantitative real-time polymerase chain reaction (qRT-PCR), Enzyme-Linked Immunosorbent Assay (ELISA), Immunofluorescence (IF) and Western Blot (WB).

RESULTS

Bioinformatics analysis and molecular docking identified MAPK14 as a key target of G-Rh2. In BV2 cells experiments, G-Rh2 reduced the expression and generation of inflammatory factors, reactive oxygen species (ROS), and transcription factors involved in the MAPK signaling pathway. G-Rh2 showed a decrease in inflammatory reaction and improvements in motor function in the mouse model using the modified Allen's approach for SCI.

CONCLUSION

G-Rh2 mitigates inflammatory responses and enhances motor function recovery in mice with SCI via the ROS/MAPK14 signaling pathway.

摘要

背景

抑制神经系统炎症是脊髓损伤(SCI)治疗的重要组成部分。源自植物的化合物可减少脊髓损伤,以恢复神经功能并阻断炎症反应。人参中的20(S)-人参皂苷Rh2(G-Rh2)具有抗炎特性,可通过激活丝裂原活化蛋白激酶(MAPK)信号通路来抑制MAPK14蛋白的表达。因此,本研究利用细胞和动物模型探讨了G-Rh2对脊髓损伤的抗炎作用。

方法

为了探究G-Rh2在脊髓损伤中的抗炎潜力,我们采用生物信息学分析来预测与G-Rh2和脊髓损伤相关的靶蛋白和信号通路。我们利用BV2小胶质细胞建立脂多糖(LPS)诱导的炎症模型,并在小鼠脊髓损伤模型中采用改良的Allen法。我们的研究使用了一系列方法,包括定量实时聚合酶链反应(qRT-PCR)、酶联免疫吸附测定(ELISA)、免疫荧光(IF)和蛋白质免疫印迹(WB)。

结果

生物信息学分析和分子对接确定MAPK14是G-Rh2的关键靶点。在BV2细胞实验中,G-Rh2降低了炎症因子、活性氧(ROS)以及参与MAPK信号通路的转录因子的表达和生成。在小鼠脊髓损伤模型中,采用改良Allen法,G-Rh2显示出炎症反应减轻和运动功能改善。

结论

G-Rh2通过ROS/MAPK14信号通路减轻脊髓损伤小鼠的炎症反应并增强运动功能恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/12223431/a2932d37b3e1/ga1.jpg

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