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中国药学(英文版) ›› 2025, Vol. 34 ›› Issue (3): 251-259.DOI: 10.5246/jcps.2025.03.019

• 【研究论文】 • 上一篇    

基于网络药理学研究桑黄酮G治疗糖尿病性脑病作用机制研究

张玉倩1, 牛海英2, 张晓炜1, 解伟伟1, 张恺玥1, 张兰桐3, 靳怡然1,*()   

  1. 1. 河北医科大学第二医院, 河北 石家庄 050000
    2. 河北医科大学第一医院, 河北 石家庄 050000
    3. 河北医科大学, 河北 石家庄 050000
  • 收稿日期:2024-11-23 修回日期:2025-01-06 接受日期:2025-02-08 出版日期:2025-03-31 发布日期:2025-04-01
  • 通讯作者: 靳怡然

Elucidating the mechanism of Kuwanon G in treating diabetic encephalopathy through network pharmacology: A comprehensive study

Yuqian Zhang1, Haiying Niu2, Xiaowei Zhang1, Weiwei Xie1, Kaiyue Zhang1, Lantong Zhang3, Yiran Jin1,*()   

  1. 1 The Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei, China
    2 The first Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei, China
    3 Hebei Medical University, Shijiazhuang 050000, Hebei, China
  • Received:2024-11-23 Revised:2025-01-06 Accepted:2025-02-08 Online:2025-03-31 Published:2025-04-01
  • Contact: Yiran Jin
  • Supported by:
    Hebei Administration of Traditional Chinese Medicine (Grant No. 2024040).

摘要:

本研究旨在通过采用网络药理学研究桑黄酮G治疗糖尿病脑病的作用机制。通过Pharmmapper数据库确定桑黄酮G的作用靶点, GeneCards database, DisGeNET和Therapeutic Target等数据库筛选糖尿病脑病的潜在靶点。利用STRING 12.0进行蛋白质互作分析, 构建PPI网络以筛选重要靶点; 运用David数据库对靶点进行GO和KEGG富集分析, 运用Cytoscape软件筛选出关键基因。结果显示桑黄酮G有101个潜在靶点, 糖尿病脑病共有1058个潜在靶点。两者有34个共同靶基因。GSK3B、CASP3、MAKP14、ESR1和PPARG被认为是桑黄酮G治疗糖尿病脑病的关键基因。KEGG富集通路的分析显示, 桑黄酮G治疗糖尿病脑病的主要通路包括调节脂质与动脉粥样硬化、流体剪切应力与动脉粥样硬化相关通路、IL-17信号通路和AGE-RAGE信号通路。本研究表明桑黄酮G可以通过多靶点、多通路改善糖尿病脑病, 为进一步研究糖尿病脑病的治疗提供了新的思路。

关键词: 桑黄酮G, 网络药理学, 糖尿病脑病, 作用机制

Abstract:

The present study employed network pharmacology to elucidate the molecular mechanism underlying the therapeutic effects of kuwanon G in diabetic encephalopathy. Utilizing the Pharmmapper databases, we identified potential targets associated with kuwanon G. Simultaneously, targets related to diabetic encephalopathy were screened. The VENNY software facilitated the identification of 34 common target genes, forming the basis for constructing a protein-protein interaction network map via the STRING database. GO enrichment and KEGG pathway analyses were conducted using the David database, with Cytoscape software employed to pinpoint key target genes. Results revealed 101 potential targets for kuwanon G and 1058 for diabetic encephalopathy, with an overlap of 34 target genes. Notably, GSK3B, CASP3, MAKP14, ESR1, and PPARG emerged as pivotal genes in the therapeutic action of kuwanon G against diabetic encephalopathy. Pathway analysis of these key genes indicated that kuwanon G exerted its therapeutic effects through modulating pathways associated with lipid and atherosclerosis, fluid shear stress and atherosclerosis, IL-17 signaling, and the AGE-RAGE signaling pathway. This study offered valuable insights into the potential molecular mechanisms of kuwanon G in treating diabetic encephalopathy, presenting a novel framework for future research in this domain.

Key words: Kuwanon G, Network pharmacology, Diabetic encephalopathy, Mechanism

Supporting: