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首页|期刊导航|核农学报|基于网络药理学和细胞试验探究黄精干预Ⅱ型糖尿病的作用机制

基于网络药理学和细胞试验探究黄精干预Ⅱ型糖尿病的作用机制

奚林芝 郑琳 王丹丹 刘利萍

核农学报2026,Vol.40Issue(2):279-289,11.
核农学报2026,Vol.40Issue(2):279-289,11.DOI:10.11869/j.issn.1000-8551.2026.02.0279

基于网络药理学和细胞试验探究黄精干预Ⅱ型糖尿病的作用机制

Exploring the Mechanism of Polygonatum Rhizome Intervention in Type Ⅱ Diabetes Based on Network Pharmacology and Cell Experiments

奚林芝 1郑琳 2王丹丹 1刘利萍3

作者信息

  • 1. 浙江万里学院生物与环境学院,浙江宁波 315100
  • 2. 宁波检验检疫科学技术研究院,浙江宁波 315806
  • 3. 浙江万里学院生物与环境学院,浙江宁波 315100||安徽新华学院药学院,安徽 合肥 230088
  • 折叠

摘要

Abstract

To explore the potential mechanism of Polygonatum Rhizome in intervening Type Ⅱ diabetes mellitus(T2DM),network pharmacology and cell experiments were conducted to screen its active components and corresponding targets using TCMSP database,while T2DM related targets were curated from Genecards and Omim databases.Venny tools were utilized to identify the common targets between Polygonatum Rhizome and T2DM.The David database was employed to perform Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis on these shared targets.Cytoscape software was then utilized to construct an"active component-target-pathway"interaction network.An insulin-resistant HepG2(IR-HepG2)cell model was established to assess the impacts of active components extracted from Polygonatum rhizome on cellular glucose consumption,uptake,and the expression of key targets.The results indicated that 13 active components identified from Polygonatum Rhizome,including baicalein and diosgenin,were were associated with 67 common targets such as protein kinase B(AKT1),tumor protein P53(TP53),mitogen-activated protein kinase(MAPK).These targets were enriched in 154 signaling pathways,including the phosphatidylinositol 3 kinase-protein kinase B(PI3K/AKT)pathway and the advanced glycation end products-receptor for advanced glycation end products(AGE-RAGE)pathway,both critically implicated in diabetes pathogenesis.The main active components of Polygonatum Rhizome were found to enhance glucose consumption and uptake in IR-HepG2 cells to varying degrees and upregulate the expression of AKT1 and PI3K.In conclusion,components such as baicalein and diosgenin may intervene in T2DM by targeting AKT1 and PI3K,thereby regulating the PI3K/AKT signaling pathway.The study provides a scientific foundation for developing Polygonatum Rhizome as a medicinal and edible health product aimed at type Ⅱ diabetes prevention.

关键词

黄精/Ⅱ型糖尿病/网络药理学/细胞学/作用机制

Key words

Polygonatum Rhizome/type Ⅱ diabetes mellitus/network pharmacology/cytology/mechanism of action

引用本文复制引用

奚林芝,郑琳,王丹丹,刘利萍..基于网络药理学和细胞试验探究黄精干预Ⅱ型糖尿病的作用机制[J].核农学报,2026,40(2):279-289,11.

基金项目

宁波公益(重点)科技计划项目(2022S186),浙江省"生物工程"一流学科学生创新项目(CX2023015) (重点)

核农学报

1000-8551

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