Y Zhang, S Xia, L Zhang, M Chen, X Liu, Q Gao, H Ye
{"title":"[忍冬花提取物对小鼠多柔比星所致肝损伤的保护作用]。","authors":"Y Zhang, S Xia, L Zhang, M Chen, X Liu, Q Gao, H Ye","doi":"10.12122/j.issn.1673-4254.2024.08.16","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To explore the mechanism underlying the protective effect of <i>Lonicerae japonicae</i> flos (LJF) extract against doxorubicin (DOX) -induced liver injury in mice.</p><p><strong>Methods: </strong>Network pharmacology methods were used to obtain the intersection genes between LJF targets and disease targets, based on which the protein-protein interaction (PPI) network was constructed using STRING database for screening the core targets using Cytoscape software. DAVID database was used for bioinformatics analysis, and the core components and core targets were verified using molecular docking study. In a mouse model of DOX-induced liver injury, the effect of LJF extract on liver pathologies, serum levels of ALT and AST, and hepatic expressions of HYP, ROS, TNF-α, IL-6, COL-Ⅳ and P53 proteins were evaluated using HE and Masson staining, ELISA, and Western blotting.</p><p><strong>Results: </strong>We identified 12 core targets from 43 intersection genes involving cancer pathway, IL-17 signaling pathway, and TNF signaling pathways. Molecular docking study suggested that 10 core components of LJF could bind to different core targets. The mice with DOX-induced liver injury showed elevated serum AST and ALT levels with obvious liver injury and fibrosis, increased ROS content, and enhanced expressions of TNF-α, IL-6, HYP, COL-Ⅳ and P53 proteins in the liver tissue. All these changes in the mouse models were significantly alleviated by treatment with LJF extract, suggesting obviously lowered levels of oxidative stress, inflammation and fibrosis in the liver tissues.</p><p><strong>Conclusion: </strong>LJF extract is capable of alleviating DOX-induced liver injury in mice by downregulating Trp53, TNF and IL-6 to reduce liver oxidative stress, inflammation and fibrosis.</p>","PeriodicalId":18962,"journal":{"name":"Nan fang yi ke da xue xue bao = Journal of Southern Medical University","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11378036/pdf/","citationCount":"0","resultStr":"{\"title\":\"[Protective effect of <i>Lonicerae japonicae</i> flos extract against doxorubicin-induced liver injury in mice].\",\"authors\":\"Y Zhang, S Xia, L Zhang, M Chen, X Liu, Q Gao, H Ye\",\"doi\":\"10.12122/j.issn.1673-4254.2024.08.16\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To explore the mechanism underlying the protective effect of <i>Lonicerae japonicae</i> flos (LJF) extract against doxorubicin (DOX) -induced liver injury in mice.</p><p><strong>Methods: </strong>Network pharmacology methods were used to obtain the intersection genes between LJF targets and disease targets, based on which the protein-protein interaction (PPI) network was constructed using STRING database for screening the core targets using Cytoscape software. DAVID database was used for bioinformatics analysis, and the core components and core targets were verified using molecular docking study. In a mouse model of DOX-induced liver injury, the effect of LJF extract on liver pathologies, serum levels of ALT and AST, and hepatic expressions of HYP, ROS, TNF-α, IL-6, COL-Ⅳ and P53 proteins were evaluated using HE and Masson staining, ELISA, and Western blotting.</p><p><strong>Results: </strong>We identified 12 core targets from 43 intersection genes involving cancer pathway, IL-17 signaling pathway, and TNF signaling pathways. Molecular docking study suggested that 10 core components of LJF could bind to different core targets. The mice with DOX-induced liver injury showed elevated serum AST and ALT levels with obvious liver injury and fibrosis, increased ROS content, and enhanced expressions of TNF-α, IL-6, HYP, COL-Ⅳ and P53 proteins in the liver tissue. All these changes in the mouse models were significantly alleviated by treatment with LJF extract, suggesting obviously lowered levels of oxidative stress, inflammation and fibrosis in the liver tissues.</p><p><strong>Conclusion: </strong>LJF extract is capable of alleviating DOX-induced liver injury in mice by downregulating Trp53, TNF and IL-6 to reduce liver oxidative stress, inflammation and fibrosis.</p>\",\"PeriodicalId\":18962,\"journal\":{\"name\":\"Nan fang yi ke da xue xue bao = Journal of Southern Medical University\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11378036/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nan fang yi ke da xue xue bao = Journal of Southern Medical University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.12122/j.issn.1673-4254.2024.08.16\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nan fang yi ke da xue xue bao = Journal of Southern Medical University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12122/j.issn.1673-4254.2024.08.16","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
摘要
目的探讨忍冬科植物忍冬藤(Lonicerae japonicae flos,LJF)提取物对多柔比星(Doxorubicin,DOX)诱导的小鼠肝损伤的保护作用机制:采用网络药理学方法获得忍冬藤提取物靶点与疾病靶点之间的交叉基因,在此基础上利用STRING数据库构建蛋白-蛋白相互作用(PPI)网络,使用Cytoscape软件筛选核心靶点。利用 DAVID 数据库进行生物信息学分析,并通过分子对接研究验证了核心成分和核心靶点。在DOX诱导的小鼠肝损伤模型中,使用HE和Masson染色、ELISA和Western印迹法评估了LJF提取物对肝脏病理、血清ALT和AST水平以及肝脏中HYP、ROS、TNF-α、IL-6、COL-Ⅳ和P53蛋白表达的影响:结果:我们从43个交叉基因中发现了12个核心靶点,涉及癌症通路、IL-17信号通路和TNF信号通路。分子对接研究表明,LJF的10个核心成分可与不同的核心靶点结合。DOX诱导的肝损伤小鼠血清AST和ALT水平升高,肝损伤和肝纤维化明显,ROS含量增加,肝组织中TNF-α、IL-6、HYP、COL-Ⅳ和P53蛋白表达增强。LJF提取物能显著缓解小鼠模型的所有这些变化,表明肝组织中的氧化应激、炎症和纤维化水平明显降低:结论:LJF提取物能够通过下调Trp53、TNF和IL-6,减轻肝脏氧化应激、炎症和纤维化,从而缓解DOX诱导的小鼠肝损伤。
[Protective effect of Lonicerae japonicae flos extract against doxorubicin-induced liver injury in mice].
Objective: To explore the mechanism underlying the protective effect of Lonicerae japonicae flos (LJF) extract against doxorubicin (DOX) -induced liver injury in mice.
Methods: Network pharmacology methods were used to obtain the intersection genes between LJF targets and disease targets, based on which the protein-protein interaction (PPI) network was constructed using STRING database for screening the core targets using Cytoscape software. DAVID database was used for bioinformatics analysis, and the core components and core targets were verified using molecular docking study. In a mouse model of DOX-induced liver injury, the effect of LJF extract on liver pathologies, serum levels of ALT and AST, and hepatic expressions of HYP, ROS, TNF-α, IL-6, COL-Ⅳ and P53 proteins were evaluated using HE and Masson staining, ELISA, and Western blotting.
Results: We identified 12 core targets from 43 intersection genes involving cancer pathway, IL-17 signaling pathway, and TNF signaling pathways. Molecular docking study suggested that 10 core components of LJF could bind to different core targets. The mice with DOX-induced liver injury showed elevated serum AST and ALT levels with obvious liver injury and fibrosis, increased ROS content, and enhanced expressions of TNF-α, IL-6, HYP, COL-Ⅳ and P53 proteins in the liver tissue. All these changes in the mouse models were significantly alleviated by treatment with LJF extract, suggesting obviously lowered levels of oxidative stress, inflammation and fibrosis in the liver tissues.
Conclusion: LJF extract is capable of alleviating DOX-induced liver injury in mice by downregulating Trp53, TNF and IL-6 to reduce liver oxidative stress, inflammation and fibrosis.