Fan Fei, Han Fei, Hao Long
Department of Pediatrics, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, People's Republic of China.
Department of Paediatrics, Beijing Fangshan District Liangxiang Hospital, Beijing, People's Republic of China.
Degener Neurol Neuromuscul Dis. 2022 Jul 15;12:85-96. doi: 10.2147/DNND.S370278. eCollection 2022.
, known as Suanzaoren (SZR) in Chinese, is a Chinese herbal medicine widely used in sedatives and tranquilizers. Although SZR is important for the clinical treatment of Tourette syndrome (TS), its mechanism of action remains unclear. Therefore, we investigated the pharmacological mechanisms of SZR in TS treatment using network pharmacology and systems biology approaches.
The bioactive components and potential targets of SZR were screened using the TCMSP database. UniProt was used to identify targets by mapping the known genes related to SZR. The known genes related to TS were identified by GeneCards and OMIM databases. A protein-protein interaction network was constructed using information from STRING 11.0 database. Cytoscape 3.8.0 software and Bioinformatics online platform were used for plotting this network. Gene ontology and KEGG enrichment analyses were performed using Metascape. Finally, AutoDock was used to verify the molecular docking.
We found that SZR had 10 active compounds. There were 30 overlapping target genes between TS and SZR. These genes were associated with several signaling and metabolic pathways. , and were the top three hub genes. The active components in SZR had a high binding affinity for the key targets.
SZR therapy for TS could achieve network regulation through the action of various active components of Chinese medicine on different targets and generate a complex regulatory relationship via interaction with potential targets, thereby playing a therapeutic role. Thus, SZR is a potential candidate for treating TS because it regulates nervous system functions.
酸枣仁在中国被称为酸枣仁(SZR),是一种广泛用于镇静和安神的中药。尽管酸枣仁对抽动秽语综合征(TS)的临床治疗很重要,但其作用机制仍不清楚。因此,我们使用网络药理学和系统生物学方法研究了酸枣仁治疗TS的药理机制。
使用TCMSP数据库筛选酸枣仁的生物活性成分和潜在靶点。通过映射与酸枣仁相关的已知基因,使用UniProt来识别靶点。通过GeneCards和OMIM数据库识别与TS相关的已知基因。利用STRING 11.0数据库的信息构建蛋白质-蛋白质相互作用网络。使用Cytoscape 3.8.0软件和生物信息学在线平台绘制该网络。使用Metascape进行基因本体和KEGG富集分析。最后,使用AutoDock验证分子对接。
我们发现酸枣仁有10种活性化合物。TS和酸枣仁之间有30个重叠的靶基因。这些基因与几种信号和代谢途径相关。 、 和 是前三个枢纽基因。酸枣仁中的活性成分对关键靶点具有高结合亲和力。
酸枣仁治疗TS可通过中药的各种活性成分作用于不同靶点实现网络调节,并通过与潜在靶点相互作用产生复杂的调节关系,从而发挥治疗作用。因此,酸枣仁是治疗TS的潜在候选药物,因为它调节神经系统功能。