摘要
为探讨红曲中桔霉素导致毒性的内在机理,通过搜索Swiss Target Prediction、Similarity ensemble approach、Comparative Toxicogenomics Database和GeneCards数据库,利用Metascape、Kobas 3.0、Cytoscape 3.7.2和AutoDock软件,开展了网络药理学分析。结果显示,通过筛选去重获得桔霉素与“liver toxicity”和“kidney toxicity”相关的潜在靶点110个,GO富集分析功能条目496条,其中涉及分子功能、生物过程和细胞组成的条目分别为97、354和45条。KEGG信号通路富集靶点数和显著性均较高的是肿瘤MicroRNA通路、肿瘤通路、乙型肝炎等通路。桔霉素可能通过TP53、CASP3、MAPK3和ALB等关键靶点导致肝肾毒性。分子对接实验证明,桔霉素与靶点可以结合,揭示了桔霉素导致肝肾毒性的潜在作用靶点和信号通路,为进一步研究桔霉素致毒机理和健康防护提供理论参考。
In order to explore the mechanism of toxicity induced by citrinin in Monascus,the databases of Swiss Target Prediction,Similarity ensemble approach,Comparative Toxicogenomics Database and GeneCards were searched,and the software of Metascape,Kobas 3.0,Cytoscape 3.7.2 and AutoDock were employed for network pharmacology analysis.The results showed that a total of 110 potential targets,which showed the relationship between citrinin and liver toxicity as well as kidney toxicity,were achieved after filter and deduplication.There were 496 items enriched by GO analysis,including 97 molecular function,354 biological process and 45 cell composition.The KEGG signal pathways with more enriched targets and higher significance mainly included MicroRNAs in cancer,Patyways in cancer,Hepatitis B and so on.Citrinin might induce hepatorenal toxicity through targets of TP53,CASP3,MAPK3 and ALB,and the molecular docking experiments showed that citrinin could bind to these targets.The potential targets and related signal pathways of citrinin-induced hepatorenal toxicity were revealed,providing theoretical reference for further study on the mechanism of citrinin-induced toxicity and health protection.
作者
唐光甫
桂艳玲
满海乔
刘畅
赵杰宏
TANG Guangfu;GUI Yanling;MAN Haiqiao;LIU Chang;ZHAO Jiehong(Key Lab of Pharmacognostics of Guizhou Province,Guizhou University of Traditional Chinese Medicine,Guiyang 550002,China)
出处
《食品与生物技术学报》
CAS
CSCD
北大核心
2023年第2期90-96,共7页
Journal of Food Science and Biotechnology
基金
贵州省科技支撑计划项目(黔科合支撑[2019]2776号)。
关键词
红曲霉
网络药理学
桔霉素
潜在靶点
肝肾毒性
分子对接
Monascus
network pharmacology
citrinin
potential target
liver and kidney toxicity
molecular docking
