中国药物警戒 ›› 2026, Vol. 23 ›› Issue (7): 829-834.
DOI: 10.19803/j.1672-8629.20260072

• 综述 • 上一篇    下一篇

中药抗肝纤维化信号通路研究进展

张晨璐, 李明奇, 王映荷, 马月宏*   

  1. 内蒙古医科大学基础医学院,内蒙古自治区分子病理学重点实验室,内蒙古 呼和浩特 010110
  • 收稿日期:2026-01-21 出版日期:2026-07-15 发布日期:2026-07-16
  • 通讯作者: *马月宏,男,教授·博导,中蒙药抗肝纤维化药理。E-mail: myh19982002@sina.com
  • 作者简介:张晨璐,女,在读硕士,中蒙药抗肝纤维化药理。
  • 基金资助:
    国家自然科学基金资助项目(82460819、81960759); 内蒙古自治区自然科学基金资助项目(2024LHMS08029、2019MS08010); 内蒙古自治区重点研发和成果转化计划项目(2026YFSH0099); 内蒙古自治区“英才兴蒙”工程蒙药抗肝纤维化研究团队(2026TEL30); 内蒙古医科大学致远人才项目治学人才(ZY20241201); 内蒙古人才开发基金(22056); 内蒙古医科大学重点项目(YKD2022ZD019); 内蒙古医科大学蒙药抗肝纤维化作用研究科技创新团队(YKD2022TD039)

Research progress in signal pathways of traditional Chinese medicine in anti-liver fibrosis

Zhang Chenlu, Li Mingqi, Wang Yinghe, Ma Yuehong*   

  1. College of Basic Medical Sciences, Inner Mongolia Medical University, Hohhot Inner Mongolia 010110, China
  • Received:2026-01-21 Online:2026-07-15 Published:2026-07-16

摘要: 目的 探讨中药单体及复方在肝纤维化治疗中的多靶点、多通路干预机制,为西药单靶点治疗提供参考。方法 梳理近年来国内外关于中药抗肝纤维化研究文献,归纳其主要干预的信号通路网络(TGF-β/Smad、PI3K/Akt、NOX4/ROS、MAPK、JAK/STAT3、NF-κB、Notch、Wnt/β-Catenin等),分析中药“多靶点-多通路-多环节”协同调控的作用特点及分子机制。结果 中药可通过同时干预肝纤维化关键信号网络,实现抑制肝星状细胞(HSC)激活、阻断胶原沉积、促进基质降解、诱导HSC凋亡等多重效应,在逆转早期纤维化展现出独特优势。结论 深入开展中药抗肝纤维化活性成分的精准识别与靶点验证,结合现代组学技术与网络药理学方法优化配伍策略,为肝纤维化的防治提供参考。

关键词: 肝纤维化, 中药, 信号通路, 肝星状细胞, 信号转导

Abstract: Objective To investigate the multi-target and multi-pathway intervention mechanisms of traditional Chinese medicine (TCM) monomers and compound formulas in the treatment of hepatic fibrosis in order to provide data for efforts to overcome the limitations of single-target Western medicine therapy. Methods Research papers on TCM against hepatic fibrosis published in recent years were retrieved and reviewed. The main signaling pathway networks with interventions by TCM (including TGF-β/Smad, PI3K/Akt, NOX4/ROS, MAPK, JAK/STAT3, NF-κB, Notch, Wnt/β-Catenin, etc.) were summarized. The characteristics and molecular mechanisms of “multi-target, multi-pathway, and multi-link” synergistic regulation were analyzed. Results TCM could simultaneously intervene in key signaling networks of hepatic fibrosis via multiple therapeutic effects, such as inhibition of hepatic stellate cell (HSC) activation, blockade of collagen deposition, promotion of matrix degradation, and induction of HSC apoptosis, which gave TCM advantages in reversing early-stage fibrosis. Conclusion More research should be devoted to the precise identification of active components and target validation of TCM against hepatic fibrosis while compatibility strategies are to be optimized based on modern omics technologies and network pharmacology so as to contribute to precise prevention and treatment of hepatic fibrosis.

Key words: Liver Fibrosis, Traditional Chinese Medicine, Signaling Pathway, Hepatic Stellate Cell, Signal Transduction

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