首页|基于网络药理分子对接技术及实验验证探究十味接骨方治疗骨关节炎的作用靶点及机制

基于网络药理分子对接技术及实验验证探究十味接骨方治疗骨关节炎的作用靶点及机制

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目的 基于网络药理学及分子对接技术研究十味接骨方治疗骨关节炎的潜在作用靶点及机制。方法 利用中药系统药理学数据库筛选十味接骨方的活性成分及对应靶点,并通过GeneCards、Digsee、DisGeNET数据库获取骨关节炎疾病靶点。然后将药物活性成分靶点及疾病靶点的交集录入STRING数据库,构建两者相互作用网络。采用clusterProfiler 3。8。1将所得交集靶点信息进行GO与KEGG富集分析。利用AutoDock 4。2。6软件对重要活性成分与靶点进行分子对接验证。采用细胞计数试剂盒-8及实时荧光定量多聚核苷酸链式反应技术对经十味接骨方处理后软骨细胞的细胞活力及骨关节炎关键基因的RNA表达进行检测。结果 共得到679个药物活性成分及2 411个作用靶点。主要活性成分为:木犀草素、乌索酸及汉黄芩素等。相关靶点主要为:蛋白激酶B(AKT1)、肿瘤坏死因子(TNF)、白细胞介素-6(IL-6)、血管生长因子A(VEGFA)、白细胞介素-1B(IL-1B)、肿瘤蛋白P53(TP53)、胱天蛋白酶3(CASP3)、前列腺素内过氧化物合酶2(PTGS2)、表皮生长因子受体(EGFR)、基质金属蛋白酶-9(MMP-9)等。富集分析结果显示十味接骨方抑制骨关节炎发生的关键通路为脂质与动脉粥样硬化信号通路。分子对接结果表明十味接骨方的主要活性成分木犀草素、乌索酸、汉黄芩素与骨关节炎关键靶点TNF、IL-6、VEGFA有较好的结合能。细胞活力及细胞增殖结果表明十味接骨方可以有效促进软骨细胞的生长增殖。基因及蛋白表达结果表明十味接骨方可以显著下调骨关节炎关键蛋白TNF、IL-6、VEGFA的表达。结论 十味接骨方可能是通过组方中的木犀草素、乌索酸和汉黄芩素等主要活性成分调控脂质与动脉粥样硬化通路中TNF、VEGFA、IL-6等关键蛋白的表达,抑制骨关节炎的发展。
Exploring the target and mechanism of Shiwei Jiegu formulation in the treatment of osteoarthritis based on network pharmacology,molecular docking technology and experimental verification
Objective To study the potential target and mechanism of Shiwei Jiegu formulation in the treatment of osteoarthritis based on network pharmacology and molecular docking technology.Methods The active constituents and corresponding targets of Shiwei Jiegu formulation were screened using pharmacology database of the traditional Chinese medicine systems,and the disease targets of osteoarthritis were obtained from GeneCards,Digsee and DisGeNET databases.Then,the intersection of drug active ingredient targets and disease targets was input into STRING database to construct the interaction network.The intersection target information was enriched by GO and KEGG using clusterProfiler 3.8.1.AutoDock 4.2.6 software was used to verify the molecular docking between important active ingredients and targets.The cell viability of chondrocytes and the RNA expression of key genes of osteoarthritis were detected by CCK-8 kit and RT-PCR.Results A total of 679 active ingredients and 2 411 targets were obtained.The main active ingredients were luteolin,ursolic acid,wogonin,etc.The main related targets were AKT1,TNF,IL-6,VEGFA,IL-1B,TP53,CASP3,PTGS2,EGFR,MMP-9,etc.The results of enrichment analysis showed that the key pathway of inhibiting osteoarthritis by Shiwei Jiegu formulation was lipid and atherosclerosis signaling pathway.The results of molecular docking indicated that the main active components of Shiwei Jiegu formulation,that luteolin,ursolic acid and wogonin had good binding energy with TNF,IL-6 and VEGFA of the key targets of osteoarthritis.The results of cell viability and cell proliferation indicated that Shiwei Jiegu formulation could effectively promote the growth and proliferation of chondrocytes.The results of gene and protein expression showed that Shiwei Jiegu formulation could significantly down-regulate the expression of TNF,IL-6 and VEGFA of the key genes in osteoarthritis.Conclusion Shiwei Jiegu formulation may regulate the expression of key proteins such as TNF,VEGFA and IL-6 in lipid and atherosclerotic pathway through the main active components such as luteolin,ursolic acid and wogonin,and inhibit the development of osteoarthritis.

Shiwei Jiegu formulationFormulationLuteolinUrsolic acidWogoninOsteoarthritisNetwork pharmacologyTarget predictionMechanism

乞超、程璐、胡松

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武汉市第一医院药学部(武汉 430022)

十味接骨方 方剂 木犀草素 乌索酸 汉黄芩素 骨关节炎 网络药理学 靶点预测 机制

湖北省中医药管理局中医药科研项目武汉市科技局知识创新专项

ZY2023Q0182023020201010181

2024

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2024.27(6)