藏药沙棘总黄酮防治慢性支气管炎的网络药理学研究 点击下载
| 论文标题： | 藏药沙棘总黄酮防治慢性支气管炎的网络药理学研究 |
| 英文标题： | |
| 中文摘要： | 目的：探讨藏药沙棘总黄酮（TFH）防治慢性支气管炎的潜在作用机制，为其进一步开发利用提供参考。方法：利用中药系统药理学分析平台数据库筛选TFH有效成分，通过PharmMapper网络服务系统、BATMAN-TCM网络药理学研究平台、DrugBank数据库、OMIM数据库预测并匹配TFH有效成分作用于慢性支气管炎的潜在靶点（即靶基因），借助生物分子功能注释系统3.0进行GO富集和KEGG通路注释分析，采用Cytoscape 3.5.1软件构建TFH防治慢性支气管炎的“成分-靶点-通路”网络，并进行网络拓扑学分析。结果：共筛选出槲皮素、表儿茶素、槲皮素-3-甲基醚等13个TFH有效成分，涉及PIK3CG、PRKCA、ALOX5基因等30个潜在作用靶点。上述靶点多分布于细胞膜和细胞质中，且主要通过蛋白质氨基酸磷酸化反应、信号转导等生物过程以及蛋白结合、转移酶活性调节等分子功能来发挥对慢性支气管炎的防治作用。上述靶点共涉及64条通路，靶点富集数量排名前10位的通路分别为Fc epsilon RI信号通路、血管内皮生长因子信号通路、丝裂原激活的蛋白激酶信号通路、T细胞受体信号通路、胶质瘤、ErbB信号通路、Toll样受体信号通路、自然杀伤细胞介导的细胞毒性、非小细胞肺癌、黏着斑。TFH防治慢性支气管炎的“成分-靶点-通路”网络共有107个节点、449条边，平均节点度值为8.299，网络中心度为0.411。其中，Fc epsilon RI信号通路、血管内皮生长因子信号通路和丝裂原激活的蛋白激酶信号通路是该网络的核心通路（节点度值≥9，中介中心性＞0.001），MAPK1、PIK3CG、AKT1等基因是该网络的核心靶点（节点度值≥40，中介中心性＞0.1）。结论：TFH有效成分槲皮素、表儿茶素、槲皮素-3-甲基醚等可能通过Fc epsilon RI信号通路、丝裂原激活的蛋白激酶信号通路、血管内皮生长因子信号通路等作用于MAPK1、PIK3CG、AKT1等靶点，进而发挥对慢性支气管炎的防治作用。 |
| 英文摘要： | OBJECTIVE： To investigate the potential prevention and treatment mechanism of total flavonoids of Tibetan medicine Hippophae rhamnoidesh （TFH） on chronic bronchitis， and to provide reference for further development and utilization. METHODS： TCM system pharmacology analysis platform database （TCMSP） was used to screen effective components of TFH. PharmMapper network service system， BATMAN-TCM network pharmacology research platform， DrugBank database and OMIM database were all used to predict and match effective components of TFH on the potential target （target gene） of chronic bronchitis. GO enrichment and KEGG pathway annotation analysis were conducted by biomolecular function annotation system 3.0. Cytoscape 3.5.1 software was used to establish TFH “component-target-pathway” network for the prevention and treatment of chronic bronchitis. The network topology was also analyzed. RESULTS： The network analysis indicated that there were 13 active components in TFH， such as quercetin， ent-epicatechin and quercetin-3-methylethter， which could interact with 30 potential targets， such as PIK3CG， PRKCA， ALOX5， etc. Above targets were mainly distributed in cell membrane and cytoplasm. TFH played prevention and treatment effect through biological processes as protein amino acid phosphorylation reaction， signal transduction， and molecular functions such as protein binding， transferase activity regulation. Above targets involved 64 pathways in total. Top 10 pathways in the list of target enrichment number were Fc epsilon RI signaling pathway， VEGF signaling pathway， MAPK signaling pathway， T cell receptor signaling pathway， glioma， ErbB signaling pathway， Toll-like receptor signaling pathway， natural killer cell mediated pathway， non-small cell lung cancer and focal adhesion. There were 107 nodes， 449 edges， 8.299 flatness and 0.411 network centricity in the “component-target-pathway” network for the prevention and treatment of chronic bronchitis. Fc epsilon RI signaling pathway， VEGF signaling pathway and MAPK signaling pathway were the core pathways of this network （node degree≥9， intermediary centrality＞0.001）. MAPK1， PIK3CG and AKT1 were the core targets of the network （node degree≥40， intermediary centrality＞0.1）. CONCLUSIONS： The effective components of TFH as quercetin， ent-epicatechin， quercetin-3-methylethter act on the targets of MAPK1， PIK3CG and AKT1 through Fc epsilon RI signaling pathway， VEGF signaling pathway and MAPK signaling pathway， and then play a role in the prevention and treatment of chronic bronchitis. |
| 期刊： | 2018年第29卷第22期 |
| 作者： | 任青措，余羊羊，切尼项毛，扎西卓玛，降拥四郎，张艺，泽翁拥忠 |
| 英文作者： | REN Qingcuo，YU Yangyang，QIENIXIANGMAO，ZHAXIZHUOMA，JIANGYONGSILANG，ZHANG Yi，ZEWENGYONGZHONG |
| 关键字： | 网络药理学；藏药；沙棘；沙棘总黄酮；慢性支气管炎；作用机制 |
| KEYWORDS： | Network pharmacology； Tibetan medicine； Hippophae rhamnoides； Total flavonoids of Hippophae rhamnoidesh； Chronic bronchitis； Mechanism |
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