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Network pharmacology of threatened abortion treated by ShouTaiWan

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摘要 Objective: To explore the mechanism of ShouTaiWan's intervention in the treatment of Threatened Abortion based on Network Pharmacology. Methods: The effective active ingredients and targets in ShouTaiWan were obtained by searching in TCMSP database, BATMAN-TCM database and Uniprot database. The target of threatened abortion was obtained by searching for 'threatened abortion' in GeneCards. And the co-target gene of ShouTaiWan and threaten abortion can be obtained through the use of gene mapping in Venn diagram. Then an interaction network "disease-drug-target" can be constructed through a software called Cytoscape. Upload the Co-targeted gene to the STRING database to construct the protein interaction network map (PPI) , which would be screened for the key genes by using R language. Finally, used the R language to analyze gene ontology (GO) enrichment and kyoto encyclopedia of genes and genome (KEGG) pathway enrichment. Result: It is predicted that 21 effective active ingredients for the treatment of threatened abortion and 89 common effective targets are expected. Quercetin, kaempferol, beta-sitosterol, and isorhamnetin were the most effective components. As for the targets, prostaglandin endoperoxidase receptor (PTGS2), progesterone receptor (PGR), prostaglandin endoperoxidase receptor 1 (PTGS1), and Peroxisome proliferator activates receptor gamma (PPARG) were the most effective ones. The core targets in PPI network are Interleukin-6 (IL-6), protein kinase (AKT1), vascular endothelial growth factor A (VEGFA), etc. GO enrichment analysis shows that the activity of cytokines, regulatory functions, nuclear protein receptors and transcription of genes would be affected. KEGG pathway enrichment analysis illustrates that advanced glycation end products-receptor for AGE (AGE-RAGE) pathways are of the highest significance, followed by the fluid shear stress and atherosclerosis pathways. Conclusion: ShouTaiWan can achieve anti-inflammatory, increase vascular permeability,improve endometrial receptivity and other aspects of regulation to treat threatened abortion and embryo implantation through regulating cytokine.
出处 《Journal of Hainan Medical University》 2020年第13期60-66,共7页 海南医学院学报(英文版)
基金 Special research project of Chinese medicine industry(No.201507001-02) National administration of traditional Chinese medicine(No.1199ws02)
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  • 1Vane J R.Inhibition of prostaglandin synthesis as a mechanism of action for aspirin-like drugs[J].Nature,1971,231(25):232-235.
  • 2Silverstein F E,Faich G,Goldstein J L,et al.Gastrointestinal toxicity with celecoxib vs nonsteroidal anti-inflammatory drugs for osteoarthritis and rheumatoid arthritis:the CLASS study:a randomized controlled trial[J].Jama,2000,284(10):1247-1255.
  • 3Graham D Y,Smith J L.Aspirin and the stomach[J].Ann Intern Med,1986,104(3):390-398.
  • 4Cayla G,Collet J P,Silvain J,et al.Prevalence and clinical impact of upper gastrointestinal symptoms in subjects treated with low dose aspirin:the UGLA survey[J].Int J Cardiol,2012,156(1):69-75.
  • 5Awad A B,Chinnam M,Fink C S,et al.β-Sitosterol activates Fas signaling in human breast cancer cells[J].Phytomedicine,2007,14(11):747-754.
  • 6Alappat L,Valerio M,Awad A B.Effect of vitamin D andβ-Sitosterol on immune function of macrophages[J].Int Immunopharmacol,2010,10(11):1390-1396.
  • 7Navarrete A,Trejo-Miranda J L,Reyes-Trejo L.Principles of root bark of hippocratea excelsa with gastroprotective activity[J].J Ethnopharmacol,2002,79(3):383-388.
  • 8Arrieta J,Benitez J,Flores E,et al.Purification of gastroprotective triterpenoids from the stem bark of EM[J].Planta Medica,2003,69(10):905-909.
  • 9牛国敏,张复华,杨国雷,凌奕文,潘焕玉,徐嘉愉.Cox-2在槲皮素抑制耐药白血病HL-60、HL-60A细胞增殖中的作用[J].右江民族医学院学报,2015,37(1):14-16. 被引量:7
  • 10陶晓薇,毛其芬.槲皮素对人胶质母细胞瘤T98G凋亡及HSP27蛋白表达的干预作用[J].浙江中西医结合杂志,2015,25(5):436-438. 被引量:4

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