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基于网络药理学和细胞实验探究青藤碱抗衰老的作用机制

付晓俐 肖嘉琪 潘欣仪 李朋坤 全羽欣 包永芬 瞿利花 单士刚

湖北科技学院学报(医学版)2026,Vol.40Issue(1):17-22,6.
湖北科技学院学报(医学版)2026,Vol.40Issue(1):17-22,6.DOI:10.16751/j.cnki.2095-4646.2025050701

基于网络药理学和细胞实验探究青藤碱抗衰老的作用机制

Investigating the Anti-Aging Mechanism of Sinomenine Using Network Pharmacology and Cell Experiments

付晓俐 1肖嘉琪 1潘欣仪 1李朋坤 2全羽欣 1包永芬 3瞿利花 4单士刚5

作者信息

  • 1. 湖北科技学院医学部药学院,湖北 咸宁 437100
  • 2. 湖北科技学院医学部临床医学院
  • 3. 湖北科技学院附属第二医院
  • 4. 湖北科技学院医学部基础医学院
  • 5. 湖北科技学院糖尿病心脑血管病变湖北省重点实验室
  • 折叠

摘要

Abstract

Objective To explore the effect of sinomenine(SIN)on D-galactose-induced macrophage senescence by using network pharmacology and cell experiments.Methods Data sources such as PubChem,SwissTargetPrediction,PharmMapper,and GeneCards were used to obtain common genes related to sinomenine and senescence.GO and KEGG pathway enrichment analyses were performed using the DAVID database and the Microbial Information Platform.A compound-target network was constructed using Cytoscape 3.10.2,and a protein-protein interaction(PPI)network was plotted to identify core genes.RAW264.7 cells were cultured in vitro and divided into three groups:the control group,the D-galactose-induced senescence model group,and the D-galactose+sinomenine group.The effect of sinomenine on RAW264.7 cell senescence was evaluated by β-galactosidase staining associated with senescence,and Western blot was used to detect chan-ges in p53 and p-AKT1/AKT1 protein expression.Results The enrichment analysis involved a total of 914 signaling pathways,541 biological processes,144 molecular functions,and 73 cellular components,mainly focusing on pathways related to cancer pathogenesis,and the PI3K-AKT signaling pathway in SIN therapy for aging.Compared with the normal control group,the proportion of β-galactosidase-positive cells and the expression of p53 protein were increased,while the expression of p-AKT1/AKT1 protein was decreased in the senescence model group(all P<0.05).Compared with the senescence model group,the proportion of β-galactosidase-positive cells and the expression of p53 pro-tein were decreased,while the expression of p-AKT1/AKT1 protein was increased in the D-galactose+sinomenine group(all P<0.05).Conclusion Sinomenine can delay the senescence of RAW264.7 macrophages induced by D-galactose by regulating p-AKT1/AKT1 signa-ling pathway.

关键词

RAW264.7/衰老/青藤碱/网络药理学/D-半乳糖

Key words

RAW 264.7/Aging/Sinomenine/Network pharmacology/D-galactose

分类

医药卫生

引用本文复制引用

付晓俐,肖嘉琪,潘欣仪,李朋坤,全羽欣,包永芬,瞿利花,单士刚..基于网络药理学和细胞实验探究青藤碱抗衰老的作用机制[J].湖北科技学院学报(医学版),2026,40(1):17-22,6.

基金项目

湖北科技学院糖尿病心脑血管病变湖北省重点实验室开放基金项目(2020TNB07) (2020TNB07)

湖北科技学院学报(医学版)

2095-4646

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