Shaanxi University of Chinese Medicine, Xianyang, People's Republic of China.
Haojing College of Shaanxi University of Science & Technology, Shaanxi, Xi'an, People's Republic of China.
Drug Des Devel Ther. 2021 May 24;15:2179-2191. doi: 10.2147/DDDT.S302617. eCollection 2021.
Acute myocardial infarction (AMI) is a cardiovascular disease with a high fatality rate. In this study, we combined network pharmacology and experimental pharmacology and discovered the potential mechanism of action and the active ingredients of the lily, was discovered. The monomer compound with stronger activity was discovered through in vitro cell experiments.
Forty known compounds were isolated from . Using TCMSP, Swiss Target Prediction, metaTarFisher, GeneCards and OMIM databases, targets of drug compositions and AMI-related genes were obtained, and the differential expression genes between AMI and normal tissues were extracted through the GEO database. Then, through an online mapping tool, the intersection genes were obtained to predict the possible effective components of that can be used to treat AMI. The top five targets were selected for molecular docking via the protein-protein interaction (PPI) network to verify the binding activity between key compounds and target proteins. GO and KEGG enrichment analyses of the intersection genes were carried out with the program R to further screen key genes and effective compositions. On this basis, the compound with more optimal activity was screened and validated in vitro.
In this study, 40 known monomer components were selected, and 1112 predicted genes, 1655 disease genes, 1425 differentially expressed genes, 1206 GO functions and 127 KEGG pathways were obtained. The results of molecular docking showed that the binding of MMP9 with drug components is stable. Through the comprehensive research of network pharmacology and experimental pharmacology, it was shown that intervenes in the process of AMI through multicomponent, multitarget, and multichannel synergistic effects. It is speculated that the anti-AMI effect may be related to the regulation of the Akt/FoxO/BCl signaling pathway. Cellular experiments showed that nicotiflorin has satisfactory anti-inflammatory activity and endothelial protection and can reduce the release of nitric oxide (NO), an inflammatory medium after endothelial cell damage.
This study reveals the therapeutic effect and relative mechanism of extract of extract on AMI. Analysis revealed that nicotiflorin from is a compound with satisfactory anti-inflammatory activity and endothelial protection, which provides a new direction and treatment basis for further experimental exploration and clinical treatment.
急性心肌梗死(AMI)是一种致死率较高的心血管疾病。本研究采用网络药理学和实验药理学相结合的方法,发现了百合的潜在作用机制和活性成分。通过体外细胞实验发现了活性更强的单体化合物。
从百合中分离得到 40 种已知化合物。利用 TCMSP、Swiss Target Prediction、metaTarFisher、GeneCards 和 OMIM 数据库获得药物成分和 AMI 相关基因的靶点,通过 GEO 数据库提取 AMI 与正常组织之间的差异表达基因。然后,通过在线映射工具获得交集基因,以预测可用于治疗 AMI 的百合潜在有效成分。通过蛋白质-蛋白质相互作用(PPI)网络对前 5 个靶点进行分子对接,以验证关键化合物与靶蛋白的结合活性。利用 R 程序对交集基因进行 GO 和 KEGG 富集分析,进一步筛选关键基因和有效成分。在此基础上,筛选并验证了体外活性更优的化合物。
本研究共筛选得到 40 种已知单体成分,获得了 1112 个预测基因、1655 个疾病基因、1425 个差异表达基因、1206 个 GO 功能和 127 个 KEGG 通路。分子对接结果表明 MMP9 与药物成分的结合较为稳定。通过网络药理学和实验药理学的综合研究,表明百合通过多成分、多靶点、多途径协同作用干预 AMI 发生发展过程。推测其抗 AMI 作用可能与调节 Akt/FoxO/BCl 信号通路有关。细胞实验表明,野靛碱具有良好的抗炎活性和内皮保护作用,可减少内皮细胞损伤后炎症介质一氧化氮(NO)的释放。
本研究揭示了百合提取物对 AMI 的治疗作用及相关机制。分析表明,百合中的野靛碱是一种具有良好抗炎活性和内皮保护作用的化合物,为进一步的实验探索和临床治疗提供了新的方向和治疗依据。