Objective:Based on network pharmacology and molecular docking technology to explore the mechanism of Professor Cao Enze's application of Panax notoginseng in the treatment of membranous nephropathy.Methods:TCMSP d...Objective:Based on network pharmacology and molecular docking technology to explore the mechanism of Professor Cao Enze's application of Panax notoginseng in the treatment of membranous nephropathy.Methods:TCMSP database was used to obtain the effective components and corresponding target information of Panax notoginseng,and Gene Cards database was used to obtain the disease target genes of membranous nephropathy.The intersection targets of the two were taken and the Venn diagram was drawn.The STRING database was used to obtain the protein interaction relationship,and the PPI network diagram was constructed by Cytoscape 3.9.1 software to screen out the core targets of Panax notoginseng in the treatment of membranous nephropathy.GO function and KEGG pathway enrichment analysis were performed using the David database to obtain the potential pathway of Panax notoginseng in the treatment of membranous nephropathy.Finally,Autodock software was used to verify the molecular docking of the main active components of the drug with the core targets.Results:A total of 7 effective components such as quercetin,ginsenoside rh2,Mandenol and Stigmasterol were retrieved,and 127 potential targets of Panax notoginseng in the treatment of membranous nephropathy were screened out.By PPI network topology analysis,23 core targets such as JUN,TP53,RELA,AKT1 and MAPK1 were screened out.GO functional enrichment analysis contained 703 biological processes,55 cell components and 121 molecular functions,and KEGG signal pathway enrichment analysis enriched 171 signal pathways.The results of molecular docking showed that there was a strong binding ability between the main core targets and the main components of Panax notoginseng.Conclusion:Through network pharmacology,it is concluded that Panax notoginseng treats membranous nephropathy through multiple targets and multiple pathways,which provides a theoretical basis for subsequent basic research.展开更多
干旱缺水是限制水稻产量主要环境因素之一。为探讨孕穗期干旱胁迫对寒地粳稻干物质积累规律及产量形成影响,选用耐旱型品种东农425和干旱敏感型品种松粳6号为试验材料。通过盆栽结合人工控水方式于孕穗期控制土壤水势至0、-10、-25和-40...干旱缺水是限制水稻产量主要环境因素之一。为探讨孕穗期干旱胁迫对寒地粳稻干物质积累规律及产量形成影响,选用耐旱型品种东农425和干旱敏感型品种松粳6号为试验材料。通过盆栽结合人工控水方式于孕穗期控制土壤水势至0、-10、-25和-40 k Pa,处理21 d后恢复正常灌溉。研究孕穗期不同程度干旱胁迫对寒地粳稻干物质积累分配转运、产量及产量构成因素影响。结果表明,孕穗期干旱胁迫导致地上部干物质积累量、转运量均随土壤水势降低而下降。成熟期不同器官干物质分配表现为籽粒>茎鞘>叶,茎鞘干物质和源器官干物质分配比例及源/库随干旱程度上升而增加,而籽粒干物质分配比例与其相反。抗旱性强品种在干旱胁迫条件下有较强物质积累优势,贮藏物质转运能力明显高于抗旱性较弱品种。干旱胁迫使枝梗性状下降,对枝梗性状影响表现为二次枝梗>一次枝梗。干旱胁迫下寒地粳稻由于每穴穗数、穗粒数和结实率显著降低造成产量显著下降,降幅随土壤水势降低而逐渐上升。展开更多
基金2022 Anhui Provincial Health Research Project (No.AHWJ2022b041)2021 Anhui Provincial Key Medical and Health Specialty Construction Project (No.Anhui Health Letter 2021-273)。
文摘Objective:Based on network pharmacology and molecular docking technology to explore the mechanism of Professor Cao Enze's application of Panax notoginseng in the treatment of membranous nephropathy.Methods:TCMSP database was used to obtain the effective components and corresponding target information of Panax notoginseng,and Gene Cards database was used to obtain the disease target genes of membranous nephropathy.The intersection targets of the two were taken and the Venn diagram was drawn.The STRING database was used to obtain the protein interaction relationship,and the PPI network diagram was constructed by Cytoscape 3.9.1 software to screen out the core targets of Panax notoginseng in the treatment of membranous nephropathy.GO function and KEGG pathway enrichment analysis were performed using the David database to obtain the potential pathway of Panax notoginseng in the treatment of membranous nephropathy.Finally,Autodock software was used to verify the molecular docking of the main active components of the drug with the core targets.Results:A total of 7 effective components such as quercetin,ginsenoside rh2,Mandenol and Stigmasterol were retrieved,and 127 potential targets of Panax notoginseng in the treatment of membranous nephropathy were screened out.By PPI network topology analysis,23 core targets such as JUN,TP53,RELA,AKT1 and MAPK1 were screened out.GO functional enrichment analysis contained 703 biological processes,55 cell components and 121 molecular functions,and KEGG signal pathway enrichment analysis enriched 171 signal pathways.The results of molecular docking showed that there was a strong binding ability between the main core targets and the main components of Panax notoginseng.Conclusion:Through network pharmacology,it is concluded that Panax notoginseng treats membranous nephropathy through multiple targets and multiple pathways,which provides a theoretical basis for subsequent basic research.
文摘干旱缺水是限制水稻产量主要环境因素之一。为探讨孕穗期干旱胁迫对寒地粳稻干物质积累规律及产量形成影响,选用耐旱型品种东农425和干旱敏感型品种松粳6号为试验材料。通过盆栽结合人工控水方式于孕穗期控制土壤水势至0、-10、-25和-40 k Pa,处理21 d后恢复正常灌溉。研究孕穗期不同程度干旱胁迫对寒地粳稻干物质积累分配转运、产量及产量构成因素影响。结果表明,孕穗期干旱胁迫导致地上部干物质积累量、转运量均随土壤水势降低而下降。成熟期不同器官干物质分配表现为籽粒>茎鞘>叶,茎鞘干物质和源器官干物质分配比例及源/库随干旱程度上升而增加,而籽粒干物质分配比例与其相反。抗旱性强品种在干旱胁迫条件下有较强物质积累优势,贮藏物质转运能力明显高于抗旱性较弱品种。干旱胁迫使枝梗性状下降,对枝梗性状影响表现为二次枝梗>一次枝梗。干旱胁迫下寒地粳稻由于每穴穗数、穗粒数和结实率显著降低造成产量显著下降,降幅随土壤水势降低而逐渐上升。
