首页|椎间盘丸治疗腰椎间盘退变的网络药理学和生物信息学研究

椎间盘丸治疗腰椎间盘退变的网络药理学和生物信息学研究

扫码查看
目的 探讨椎间盘丸(zhuijianpan pill,ZJPW)治疗腰椎间盘退变的主要活性成分和分子机制.方法 从TCMSP 数据库获得 ZJPW的主要活性成分及作用靶点,从 GeneCards数据库、TTD 数据库、OMIM 数据库及 GEO 数据库筛选腰椎间盘退变的靶点.使用 Cytoscape 3.9.1 软件构建"药物-成分-靶点"网络,并对疾病靶点基因进行基因本体论(gene ontology,GO)功能和京都基因与基因组百科全书(kyoto encyclopediaof genesand genome,KEGG)富集分析.通过构建蛋白质-蛋白质相互作用(protein-protein interaction,PPI)网络筛选出腰椎间盘退变的主要致病基因,并使用分子对接技术模拟药物活性成分与疾病靶点的相互作用.最后使用 CIBERSORT 工具进行免疫浸润分析.结果 共得到 ZJPW的活性成分 233 个,主要的活性成分包括槲皮素、山奈酚、汉黄芩素等.ZJPW 的作用靶点共 1283 个,其中与腰椎间盘退变密切相关的靶点 23 个,这些靶点基因主要富集在 PI3K-Akt信号通路及人乳头瘤病毒感染相关信号通路.通过 PPI 网络筛选出腰椎间盘退变的主要致病靶点为 PTGS2、HIF1A、VEGFA、FN1和 CAV1.分子对接模拟发现 ZJPW的主要活性成分可以与这些腰椎间盘退变的主要致病靶点以较低的结合能结合.免疫浸润分析发现,HIF1A与 NK细胞激活显著正相关.结论 ZJPW的活性成分可能是通过 PTGS2、HIF1A、VEGFA、FN1 和 CAV1 调控 PI3K-Akt信号通路,在腰椎间盘退变的不同阶段发挥作用,其中 HIF1A/NK 细胞轴可能是 ZJPW抑制椎间盘退变的重要环节之一.
Network Pharmacology and Bioinformatics Study on the Treatment of Lumbar Intervertebral Disc Degeneration by Zhuijianpan Pill
Objective To investigate the main active ingredients and molecular mechanism of Zhui-jianpan pill(ZJPW)in the treatment of lumbar intervertebral disc degeneration.Methods The main active ingredients and targets of ZJPW were obtained from TCMSP database,and the targets of lumbar in-tervertebral disc degeneration were screened from GeneCards database,TTD database,OMIM database and GEO database.Cytoscape 3.9.1 software was used to construct"drug-component-target"networks and analyze gene ontology(GO)functions and Kyoto Encyclopedia of Genes and Genomes(KEGG)en-richment of disease target genes.PPI network was constructed to screen out the main pathogenic genes of lumbar intervertebral disc degeneration,and molecular docking technology was used to simulate the inter-action between drug active ingredients and disease targets.Finally,immune infiltration analysis was per-formed using the CIBERSORT tool.Results A total of 233 active ingredients of ZJPW were obtained,and the main active components included quercetin,kaempferol,and hansenin.A total of 1,283 targets of ZJPW were identified,of which 23 were closely related to lumbar disc degeneration.These target genes were mainly enriched in the PI3K-Akt signaling pathway and the signaling pathway related to hu-man papillomavirus infection.The main pathogenic targets of lumbar disc degeneration were screened by PPI network as PTGS2,HIF1A,VEGFA,FN1 and CAV1.Molecular docking simulations revealed that the main active ingredients of ZJPW could bind to these main pathogenic targets of lumbar disc degenera-tion with low binding energy.Immune infiltration analysis revealed a significant positive correlation be-tween HIF1A and NK cell activation.Conclusion The active components of ZJPW may act at different stages of lumbar disc degeneration by modulating the PI3K-Akt signaling pathway through PTGS2,HIF1A,VEGFA,FN1 and CAV1.Among them,the HIF1A/NK cell axis may be one of the important links in the inhibition of disc degeneration by ZJPW.

lumbar intervertebral disc degenerationZhuijianpan pillnetwork pharmacologymo-lecular dockingimmune infiltration

陈璐璐、李洋、吕文娟、张迪

展开 >

河南省洛阳正骨医院 河南省骨科医院脊柱外三科,郑州 450000

腰椎间盘退变 椎间盘丸 网络药理学 分子对接 免疫浸润

2024

河南医学高等专科学校学报
河南职工医学院

河南医学高等专科学校学报

影响因子:0.467
ISSN:1008-9276
年,卷(期):2024.36(1)
  • 50