Suppr超能文献

基于网络药理学和分子对接技术探索青光安颗粒治疗青光眼的分子机制

Exploring the Molecular Mechanism of Qing Guang An Granule in Treating Glaucoma Using Network Pharmacology and Molecular Docking.

作者信息

Ou Chen, Song Houpan, Zhou Yasha, Peng Jun, Peng Qinghua

机构信息

Hunan University of Chinese Medicine, Changsha, Hunan 410208, China.

出版信息

Evid Based Complement Alternat Med. 2020 Nov 23;2020:8824150. doi: 10.1155/2020/8824150. eCollection 2020.

Abstract

BACKGROUND

Qing Guang An Granule (QGAG), a Chinese patent medicine, has been used clinically to treat glaucoma for more than 20 years.

OBJECTIVE

To explore the possible mechanism of treatment of QGAG in glaucoma by using network pharmacology and molecular docking in this study.

METHODS

Active compounds and targets of each herb in QGAG were retrieved via the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). Glaucoma-related targets were acquired from OMIM and DisGeNET database. Key targets of QGAG against glaucoma were acquired by overlapping the above targets via the Venn diagram. Using the DAVID, Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis of the key targets were performed. The docking process was performed using the AutoDock 4.2.6 and AutoDock Vina 1.1.2.

RESULTS

The 55 active compounds and 173 targets were obtained and constructed a compound-target network. The 20 key targets of QGAG in treating glaucoma were acquired, and these targets are involved in the apoptotic process, cellular response to hypoxia, negative regulation of cell growth, and ovarian follicle development. The main pathways are p53, HIF-1, PI3K-Akt, and neurotrophin signaling pathway.

CONCLUSION

QGAG may exert a protective effect by acting on the optic nerve at a molecular and systemic level. This study can provide a certain basis for future researches on exploring the QGAG in treating glaucoma and provide new ideas for developing new drugs.

摘要

背景

青光安颗粒(QGAG)是一种中成药,已在临床上用于治疗青光眼20多年。

目的

本研究采用网络药理学和分子对接方法探讨青光安颗粒治疗青光眼的可能机制。

方法

通过中药系统药理学数据库及分析平台(TCMSP)检索青光安颗粒中各味中药的活性成分和靶点。从OMIM和DisGeNET数据库获取青光眼相关靶点。通过维恩图重叠上述靶点,获得青光安颗粒抗青光眼的关键靶点。利用DAVID对关键靶点进行基因本体(GO)富集分析和京都基因与基因组百科全书(KEGG)通路分析。使用AutoDock 4.2.6和AutoDock Vina 1.1.2进行对接过程。

结果

获得55种活性成分和173个靶点,构建了化合物-靶点网络。获得青光安颗粒治疗青光眼的20个关键靶点,这些靶点参与凋亡过程、细胞对缺氧的反应、细胞生长的负调控和卵泡发育。主要通路为p53、HIF-1、PI3K-Akt和神经营养因子信号通路。

结论

青光安颗粒可能通过在分子和系统水平作用于视神经发挥保护作用。本研究可为今后探索青光安颗粒治疗青光眼的研究提供一定依据,为开发新药提供新思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17fe/7704137/48156028a833/ECAM2020-8824150.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验