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首页> 外文期刊>International Journal of Experimental Diabetes Research: Experimental Diabesity Research >Based on Network Pharmacology Tools to Investigate the Molecular Mechanism of Cordyceps sinensis on the Treatment of Diabetic Nephropathy
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Based on Network Pharmacology Tools to Investigate the Molecular Mechanism of Cordyceps sinensis on the Treatment of Diabetic Nephropathy

机译:基于网络药理学工具,研究冬虫夏草对糖尿病肾病治疗的分子机制

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Background . Diabetic nephropathy (DN) is one of the most common complications of diabetes mellitus and is a major cause of end-stage kidney disease. Cordyceps sinensis (Cordyceps, Dong Chong Xia Cao) is a widely applied ingredient for treating patients with DN in China, while the molecular mechanisms remain unclear. This study is aimed at revealing the therapeutic mechanisms of Cordyceps in DN by undertaking a network pharmacology analysis. Materials and Methods . In this study, active ingredients and associated target proteins of Cordyceps sinensis were obtained via Traditional Chinese Medicine Systems Pharmacology Database (TCMSP) and Swiss Target Prediction platform, then reconfirmed by using PubChem databases. The collection of DN-related target genes was based on DisGeNET and GeneCards databases. A DN-Cordyceps common target interaction network was carried out via the STRING database, and the results were integrated and visualized by utilizing Cytoscape software. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were performed to determine the molecular mechanisms and therapeutic effects of Cordyceps on the treatment of DN. Results . Seven active ingredients were screened from Cordyceps, 293 putative target genes were identified, and 85 overlapping targets matched with DN were considered potential therapeutic targets, such as TNF, MAPK1, EGFR, ACE, and CASP3. The results of GO and KEGG analyses revealed that hub targets mainly participated in the AGE-RAGE signaling pathway in diabetic complications, TNF signaling pathway, PI3K-Akt signaling pathway, and IL-17 signaling pathway. These targets were correlated with inflammatory response, apoptosis, oxidative stress, insulin resistance, and other biological processes. Conclusions . Our study showed that Cordyceps is characterized as multicomponent, multitarget, and multichannel. Cordyceps may play a crucial role in the treatment of DN by targeting TNF, MAPK1, EGFR, ACE, and CASP3 signaling and involved in the inflammatory response, apoptosis, oxidative stress, and insulin resistance.
机译:背景 。糖尿病肾病(DN)是糖尿病最常见的并发症之一,是肾病末期肾病的主要原因。冬虫夏草(冬虫夏草,Dong Chong xia cao)是一种广泛应用的成分,用于治疗中国DN患者,而分子机制仍然尚不清楚。本研究旨在通过进行网络药理学分析揭示DN中冬虫夏草的治疗机制。材料和方法 。在本研究中,通过中医系统药理学数据库(TCMSP)和瑞士目标预测平台获得冬虫夏草中的活性成分和相关靶蛋白,然后通过使用Pubchem数据库来重新确认。 DN相关靶基因的收集基于DISGENET和Genecards数据库。通过字符串数据库进行DN-Cordyceps公共目标交互网络,通过利用Cytoscape软件集成和可视化结果。进行基因本体(GO)和京都基因组(KEGG)途径富集分析,以确定冬虫夏草对DN治疗的分子机制和治疗效果。结果 。从冬虫夏草筛选七种活性成分,鉴定了293个推定的靶基因,与DN匹配的85个重叠靶标被认为是潜在的治疗靶标,例如TNF,MAPK1,EGFR,ACE和CASP3。 Go和Kegg分析结果显示,集线器目标主要参与糖尿病并发症,TNF信号通路,PI3K-AKT信号通路和IL-17信号通路的年龄愤怒信号通路。这些靶标与炎症反应,凋亡,氧化应激,胰岛素抵抗和其他生物过程相关。结论。我们的研究表明,冬虫夏草的特征是多组分,多元和多通道。冬虫夏草可以通过靶向TNF,MAPK1,EGFR,ACE和CASP3信号传导并参与炎症反应,凋亡,氧化应激和胰岛素抵抗来发挥至多的作用。

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