Li Shaohua, Xu Guangbiao
Department of Nephrology, The First Affiliated Hospital (Southwest Hospital) of Army Medical University, Chongqing 400038, China.
Department of Nephrology, Taizhou Hospital of Zhejiang Province, Taizhou 317000, China.
Evid Based Complement Alternat Med. 2022 Jun 17;2022:6239829. doi: 10.1155/2022/6239829. eCollection 2022.
This study aimed to explore the potential mechanisms of Qishen Yiqi dripping pill (QYDP) against diabetic nephropathy (DN) through network pharmacology and animal experiments. The components and targets of QYDP and DN-related targets were retrieved from public databases. A total of 116 compounds and 160 targets of QYDP anti-DN were obtained. The top 10 hub targets including AKT1, TNF, ALB, INS, PPARG, IL-6, IL-1B, VEGF-A, JUN, and MAPK3 were screened by Cytoscape software. Then, the key targets of QYDP were enriched in 1815 Gene Ontology (GO) entries ( < 0.01) and 159 Kyoto Encyclopedia of Genomes and Genomes (KEGG) pathways ( < 0.01), mainly including the AGE-RAGE signaling pathway in diabetic complications and the PI3K-AKT signaling pathway. In animal experiments, the results of an ELISA assay showed that QYDP could regulate the expression levels of kidney function-related indexes and reduce the expression of inflammatory factors. qRT-PCR and western blot results showed that QYDP regulated the expression of hub genes. In conclusion, this study shows that QYDP could treat DN by antioxidative and antiinflammatory activity and inhibiting the PI3K-AKT signaling pathway.
本研究旨在通过网络药理学和动物实验探索芪参益气滴丸(QYDP)抗糖尿病肾病(DN)的潜在机制。从公共数据库中检索QYDP的成分和靶点以及DN相关靶点。共获得116种QYDP抗DN的化合物和160个靶点。通过Cytoscape软件筛选出前10个核心靶点,包括AKT1、TNF、ALB、INS、PPARG、IL-6、IL-1B、VEGF-A、JUN和MAPK3。然后,QYDP的关键靶点富集在1815个基因本体论(GO)条目(<0.01)和159条京都基因与基因组百科全书(KEGG)通路(<0.01)中,主要包括糖尿病并发症中的AGE-RAGE信号通路和PI3K-AKT信号通路。在动物实验中,ELISA检测结果表明QYDP可调节肾功能相关指标的表达水平并降低炎症因子的表达。qRT-PCR和western blot结果表明QYDP可调节核心基因的表达。总之,本研究表明QYDP可通过抗氧化和抗炎活性以及抑制PI3K-AKT信号通路来治疗DN。