摘要: |
目的 探讨参芪扶正液对高糖诱导心肌损伤的潜在作用机制。方法 从TCMSP、GeneCards和OMIM数据
库中分别筛选参芪扶正液活性成分、作用靶点及心肌损伤基因,通过String数据库构建蛋白质相互作用(PPI)网络,使用
Metascape数据库对交集基因进行GO、KEGG分析。H9c2 心肌细胞分别用 35 mmol/L葡萄糖或 1、5 g/L参芪扶正液处
理,MTT法检测细胞存活率,荧光染色检测细胞凋亡,Western blot检测PI3K/AKT表达。结果 发现参芪扶正液 495 个
作用靶点,心肌损伤靶点基因 2 148 个,两者交集基因为 227 个,主要涉及内分泌抵抗、HIF-1、AMPK、PI3K/AKT等信号
通路。参芪扶正液可增加心肌细胞存活,减少细胞凋亡,上调p-PI3K和p-AKT表达(P<0.05)。结论 参芪扶正液可能通
过PI3K/AKT信号减轻高糖诱导的心肌损伤。 |
关键词: 参芪扶正液 心肌损伤 网络药理学 PI3K/AKT信号通路 |
DOI: |
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基金项目:广东省中医药局中医药科研项目(20222101,20212098,20222105),广东省医学科学技术研究基金项目(A2020459),湛 江市科技发展专项资金竞争性分配项目(2021A05063) |
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Protective effect of Shenqi Fuzheng liquid on high glucose-induced myocardial injury using network pharmacology and in vitro experiment |
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Abstract: |
Objective To explore the potential mechanism of Shenqi Fuzheng liquid (SFL) on high glucose-induced
myocardial injury (MI). Methods The active ingredients and targets of SFL, and MI genes were screened from TCMSP,
GeneCards and OMIM databases, respectively. A PPI network was constructed using String database, and the intersection genes
were analyzed by GO and KEGG using Metascape database. H9c2 myocardial cells were treated with 35 mmol/L glucose or
adding with 1 and 5 g/L SFL. Survival rate, apoptosis and PI3K/AKT expression were detected by MTT, fluorescence staining
and Western blot, respectively. Results There were 495 active ingredients of SFL, 2 148 genes of MI, and 227 intersecting
genes between them. These intersecting genes were mainly involved in endocrine resistance, HIF-1, AMPK, PI3K/AKT
signaling pathways. SFL increased survival rate, reduced apoptosis, and upregulated p-PI3K/p-AKT expression of injured
myocardial cells. Conclusion SFL can alleviate high glucose-induced MI through PI3K/AKT signaling. |
Key words: Shenqi Fuzheng liquid myocardial injury network pharmacology PI3K/AKT signaling |