综合生物信息学和机器学习方法显示,Venenum bufonis通过抑制p38 MAPK/ERK-MKNK1-eIF4E信号通路对急性炎起作用
Dongjie Chen1, Ke Cai1, Jianhua Wang1
1Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Jiangsu Provincial Key Laboratory of Functional Substances in Traditional Chinese Medicine Formulae and Innovative Drug Discovery, Nanjing University of Chinese Medicine, Nanjing 210023, China.
Journal of ethnopharmacology
|February 14, 2026
概括
球菌 (VB) 通过向p38 MAPK/ERK-MKNK1-eIF4E通路,有效治疗急性喉炎 (AP). 赫勒布里根因被确定为一种关键的活性成分,可以减少炎症,并为VB提供科学基础.
科学领域:
- 药理学 药理学是指药理学的学科.
- 分子生物学分子生物学
- 生物信息学是一种生物信息学.
背景情况:
- (Venenum bufonis,简称VB) 是一种传统的亚洲治疗喉炎的药物.
- 其活性化合物和治疗机制在很大程度上仍未被描述.
研究的目的:
- 确定活性成分并阐明VB在治疗急性炎 (AP) 的机制.
主要方法:
- 生物信息学和机器学习 (ML) 用于从公共数据库中识别核心目标基因.
- 分子对接,动力学模拟和AP大鼠模型用于验证.
- 基因基因组丰富分析 (GSEA) 探索了治疗途径.
主要成果:
- 确定了三个核心点基因 (ALPL,MKNK1,CCR1) 和p38 MAPK/ERK-MKNK1-eIF4E信号通路.
- 赫勒布里根因被证实是VB的活性成分.
- 在AP大鼠模型中,VB和hellebrigenin通过抑制MKNK1和调节已识别的途径来表现出抗炎作用.
结论:
- 这项研究提供了一个系统的,数据驱动的理解VB对AP的治疗效果.
- 这些发现为VB在治疗喉炎的传统使用提供了科学理由.
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