Han Miao, Li Heng, Ke Dan, Tian Li-Ming, Hong Yi, Zhang Chong, Tian Dai-Zhi, Chen Long, Zhan Li-Rui, Zong Shi-Qin
Department of Dermatology, School of Medicine, Jianghan University, Wuhan, People's Republic of China.
Department of Dermatology, Hubei Provincial Hospital of Traditional Chinese Medicine, Hospital Affiliated to Hubei University of Chinese Medicine, Wuhan, People's Republic of China.
Clin Cosmet Investig Dermatol. 2022 Apr 27;15:763-781. doi: 10.2147/CCID.S344138. eCollection 2022.
To study the efficacy of Ba Zhen Tang in delaying skin photoaging and its potential mechanism based on network pharmacology and molecular docking.
First, we screened the active components and targets of Ba Zhen Tang by Traditional Chinese Medicine Database and Analysis Platform (TCMSP) and The Universal Protein Resource (UniProt). The target genes of skin photoaging were obtained from GeneCards and GeneMap database. Then, we analyzed the protein-protein interaction (PPI) by STRING database. The network map was constructed by Cytoscape. Finally, we performed Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis by Metascape database. The molecular docking via Autodock Vina and Pymol. Furthermore, skin photoaging cellular models were established, and the effects of Ba Zhen Tang on ameliorating skin photoaging were investigated.
A total of 160 active ingredients in Ba Zhen Tang and 60 targets of Ba Zhen Tang for delaying skin photoaging were identified. By GO enrichment analysis, 1153 biological process entries, 45 cellular component entries and 89 molecular functional entries were obtained. A total of 155 signal pathways were obtained by KEGG analysis. Ba Zhen Tang is related to MAPK signaling pathway, TNF signaling pathway and AGE-RAGE signaling pathway in diabetic complications, etc., which directly affect the key nodes of photoaging. The molecular docking results showed that there was a certain affinity between the main compounds (kaempferol, quercetin, β-sitosterol, naringenin) and core target genes (PTGS2, CASP3, MAPK1, MAPK3, TP53). Ba Zhen Tang-treated mouse serum inhibited the senescence and p16 expression of human immortalized keratinocyte (HaCaT) cells irradiated by ultraviolet-B (UVB).
Our study elucidated the potential pharmacological mechanism of Ba Zhen Tang in the treatment of photoaging through multiple targets and pathways. The therapeutic effects of Ba Zhen Tang on skin photoaging were validated in cellular models.
基于网络药理学和分子对接研究八珍汤延缓皮肤光老化的疗效及其潜在机制。
首先,通过中药系统药理学数据库与分析平台(TCMSP)和通用蛋白质资源数据库(UniProt)筛选八珍汤的活性成分和靶点。从GeneCards和GeneMap数据库获取皮肤光老化的靶基因。然后,利用STRING数据库分析蛋白质-蛋白质相互作用(PPI)。通过Cytoscape构建网络图。最后,利用Metascape数据库进行基因本体(GO)富集分析和京都基因与基因组百科全书(KEGG)通路分析。通过Autodock Vina和Pymol进行分子对接。此外,建立皮肤光老化细胞模型,研究八珍汤对改善皮肤光老化的作用。
确定了八珍汤中的160种活性成分以及八珍汤延缓皮肤光老化的60个靶点。通过GO富集分析,获得1153个生物过程条目、45个细胞成分条目和89个分子功能条目。通过KEGG分析共获得155条信号通路。八珍汤与糖尿病并发症中的MAPK信号通路、TNF信号通路和AGE-RAGE信号通路等相关,这些通路直接影响光老化的关键节点。分子对接结果表明,主要化合物(山奈酚、槲皮素、β-谷甾醇、柚皮素)与核心靶基因(PTGS2、CASP3、MAPK1、MAPK3、TP53)之间存在一定亲和力。八珍汤处理的小鼠血清抑制了紫外线B(UVB)照射后人永生化角质形成细胞(HaCaT)的衰老和p-16表达。
我们的研究阐明了八珍汤通过多靶点和多途径治疗光老化的潜在药理机制。在细胞模型中验证了八珍汤对皮肤光老化的治疗作用。