首页|基于网络药理学及体内实验探讨射麻止喘液治疗中性粒细胞型哮喘的分子机制

基于网络药理学及体内实验探讨射麻止喘液治疗中性粒细胞型哮喘的分子机制

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目的 基于网络药理学及体内实验探讨射麻止喘液治疗中性粒细胞型哮喘(NA)的分子机制.方法 (1)利用中药系统药理学数据库和分析平台(TCMSP)、文献检索及Swiss ADME、Swiss Target Prediction数据库检索、筛选射麻止喘液的活性成分及其作用靶点.利用OMIM、GeneCards、DisGeNET及DrugBank数据库检索、筛选NA疾病相关靶点.通过微生信平台对射麻止喘液活性成分作用靶点与NA疾病相关靶点取交集,得到射麻止喘液治疗NA的潜在作用靶点(共有靶点).采用Cytoscape 3.8 软件构建"中药-活性成分-潜在作用靶点"网络.通过STRING数据库建立潜在作用靶点蛋白互作(PPI)网络,使用内置Mcode插件分析获得核心靶点.使用Metascape平台对潜在作用靶点进行基因本体(GO)、京都基因和基因组百科全书(KEGG)通路富集分析.(2)将BALB/C小鼠适应性喂养 1 周后,随机分为空白组、NA模型组、射麻止喘液低剂量组(2.5 g·kg-1)、射麻止喘液高剂量组(10 g·kg-1)、地塞米松对照组(1 mg·kg-1);通过腹腔注射致敏剂[鸡卵清白蛋白(OVA)+弗氏完全佐剂(CFA)]并通过雾化吸入激发的方法复制NA小鼠模型,第 0、7、14 天分别腹腔注射OVA+CFA(20 μg OVA+75 μg CFA,0.3 mL)致敏,第 21~30 天采用 5%OVA混悬液雾化激发(每次 8 mL,每次雾化时间40 min,每天 1 次);雾化激发前 1h各组灌胃给药,地塞米松对照组腹腔注射给药,每天 1 次.采用HE染色法观察小鼠肺组织病理变化;ELISA法检测肺泡灌洗液中IL-8 含量;RT-qPCR法检测肺组织中NLRP3、CXCR2 mRNA表达水平;免疫组化法检测肺组织中p-mTOR蛋白表达水平.结果 (1)共筛选得到射麻止喘液活性成分作用靶点 826 个,NA疾病相关靶点 154 个,取交集后得到射麻止喘液治疗NA的 51 个潜在作用靶点(共有靶点).通过"中药-活性成分-潜在作用靶点"网络分析得到槲皮素、木犀草素、山柰酚、豆甾醇、柚皮素等关键活性成分.通过对潜在作用靶点的PPI网络分析得到 29 个核心靶点,包括AKT1、IL6、TNF、EGFR、NLRP3、RELA、MIF、CXCR2、VEGFA等.GO功能富集分析得到 882 个生物学过程条目、33 个细胞组分条目、61 个分子功能条目;KEGG通路富集分析得到 142 条信号通路,主要涉及TNF信号通路、甲型流感信号通路、Toll样受体通路、MAPK信号通路、mTOR信号通路等.(2)动物实验结果:与空白组比较,NA模型组小鼠的气道黏膜损伤明显,结构紊乱,有大量炎性细胞浸润,黏膜充血、水肿,肺泡壁明显增厚,肺泡腔缩小;肺泡灌洗液中的炎症因子IL-8 水平明显升高(P<0.05);小鼠肺组织NLRP3、CXCR2 mRNA表达显著上调(P<0.01),p-mTOR蛋白表达水平明显升高.与NA模型组比较,射麻止喘液低、高剂量组小鼠肺组织支气管上皮细胞结构排列可见少许紊乱,气管及血管周围有少量的炎性细胞浸润,支气管黏膜充血水肿明显减轻;小鼠肺组织CXCR2 mRNA表达显著下调(P<0.01),p-mTOR蛋白表达水平明显降低.射麻止喘液高剂量组小鼠肺泡灌洗液中的 IL-8 水平明显降低(P<0.05);射麻止喘液低剂量组小鼠肺组织 NLRP3 mRNA表达明显下调(P<0.05).结论 射麻止喘液对NA的治疗作用可能是通过槲皮素、木犀草素、山柰酚等关键活性成分,作用于NLRP3、CXCR2 等核心靶点,调控TNF信号通路、MAPK信号通路、Toll样信号通路、mTOR等关键信号通路来实现的.
Study on the Molecular Mechanism of Shema Zhichuan Liquid in the Treatment of Neutrophilic Asthma Based on Network Pharmacology and In Vivo Experiment
Objective To investigate the molecular mechanism of Shema Zhichuan Liquid in the treatment of neutrophilic asthma(NA)based on network pharmacology and in vivo experiments.Methods(1)The TCMSP,literature search and Swiss ADME and Swiss Target Prediction databases were used to search and screen the active components and their targets of Shema Zhichuan Liquid.OMIM,GeneCards,DisGeNET and DrugBank databases were used to search and screen NA disease-related targets.The intersection of the active components and NA disease-related targets of Shema Zhichuan Liquid was obtained through the microbiology platform to obtain the potential targets of Shema Zhichuan Liquid for the treatment of NA(common targets).Cytoscape 3.8 software was used to construct the network of"Chinese medicinals-active components-potential targets".The PPI network of potential targets was established by STRING database,and the core targets were obtained by analysing the built-in Mcode plug-in.The Metascape platform was used to enrich the gene ontology(GO),Kyoto Encyclopaedia of Genes and Genomes(KEGG)pathways for the potential targets.(2)BALB/C mice were acclimatised and fed for 1 week and randomly divided into a blank group,NA model group,low-dose group(2.5 g·kg-1)and high-dose group of Shema Zhichuan Liquid(10 g·kg-1),and control group of Dexamethasone(1 mg·kg-1);the NA mouse model was replicated by intraperitoneal injection of sensitizer(OVA+CFA)and nebulized inhalation excitation.OVA/CFA(20 μg OVA+75 μg CFA,0.3 mL)was injected intraperitoneally to sensitize on days 0,7 and 14 respectively,and 5%OVA suspension was nebulized on days 21-30(8 mL each time,40 minutes each time,once a day);1 hour before nebulisation,each group was administered by gastric gavage,and the Dexamethasone control group was administered by intraperitoneal injection once a day.The pathological changes of mouse lung tissue were observed by HE staining;IL-8 content in alveolar lavage fluid was detected by ELISA;mRNA expression levels of NLRP3 and CXCR2 were detected by RT-qPCR;and p-mTOR protein expression levels was detected by immunohistochemistry.Results(1)A total of 826 active component targets and 154 NA disease-related targets were obtained,and 51 potential targets(common targets)for the treatment of NA were obtained from the intersection of the active component and the NA disease-related targets of Shema Zhichuan Liquid.Through the network analysis of"Chinese medicinals-active components-potential targets",quercetin,lignocerotoxin,kaempferol,stigmasterol,naringenin and other key active components were obtained.The PPI network analysis of potential targets yielded 29 core targets,including AKT1,IL6,TNF,EGFR,NLRP3,RELA,MIF,CXCR2,VEGFA,etc..The GO functional enrichment analysis yielded 882 biological process entries,33 cellular component entries,and 61 molecular function entries;KEGG analysis yielded 142 signaling pathways,mainly involving TNF signaling pathway,influenza A signaling pathway,Toll-like receptor pathway,MAPK signaling pathway,mTOR signaling pathway and so on.(2)Results of animal experiments:compared with the blank group,mice in the NA model group showed obvious damage to the airway mucosa,structural disorders,a large number of inflammatory cells infiltration,mucosal congestion,oedema,obvious thickening of the alveolar wall,and narrowing of the alveolar lumen;the level of the inflammatory factor IL-8 in the alveolar lavage fluid was significantly elevated(P<0.05);the mRNA expressions of NLRP3 and CXCR2 in the lung tissues of the mice were significantly up-regulated(P<0.01),and the protein expression of p-mTOR was significantly increased.Compared with the NA model group,the structural arrangement of bronchial epithelial cells in the mice in the low-and high-dose groups of Shema Zhichuan Liquid was slightly disordered,with a small amount of inflammatory cell infiltration around the airways and blood vessels,and the congestion and edema of the bronchial mucosa were significantly reduced;the mRNA expression of CXCR2 in the lung tissues of the mice was significantly down-regulated(P<0.01),and the level of expression of p-mTOR protein was significantly reduced.The IL-8 level in the vesicular lavage fluid of mice in the high-dose group was significantly reduced(P<0.05);the mRNA expression of NLRP3 in the lung tissue of mice in the low-dose group was significantly down-regulated(P<0.05).Conclusion The therapeutic effect of Shema Zhichuan Liquid on NA may be achieved through the key active components,such as quercetin,lignocerol and kaempferol,acting on the core targets,such as NLRP3 and CXCR2,and regulating the key signaling pathways,such as the TNF signaling pathway,the MAPK signaling pathway,the Toll-like signaling pathway,and the mTOR pathway.

Shema Zhichuan Liquidneutrophilic asthmanetwork pharmacologyNLRP3CXCR2mTOR signaling pathwaymice

连乐燊、孟星汝、黄秀芳、周谨希、谢燕小、陶海澜、蒋紫云、刘小虹

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广州中医药大学东莞医院,广东 东莞 523000

广州中医药大学第一临床医学院,广东 广州 510405

广州中医药大学第一附属医院,广东 广州 510405

广州中医药大学岭南医学研究中心,广东 广州 510405

广州中医药大学第三临床医学院,广东 广州 510370

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射麻止喘液 中性粒细胞型哮喘 网络药理学 NLRP3 CXCR2 mTOR信号通路 小鼠

广东省基础与应用基础研究基金项目广东省基础与应用基础研究基金项目刘小虹广东省名中医传承工作室建设项目广州中医药大学东莞医院拔尖型临床人才培养项目深圳市"医疗卫生三名工程"建设项目

2023A15150108072021A1515010146粤中医办函[2018]5号东中医[2022]158号SZZYSM202206013

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(2)
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