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采用 UPLC-Q-TOF/MS 结合网络药理学分析方法系统表征金振口服液的物质基础及其药理作用机制。

Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis.

机构信息

Department of Traditional Chinese Medicine, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang District, Shenyang, Liaoning, 110016, PR China.

Jiangsu Kanion Pharmaceutical Company Ltd., Lianyungang 222001, PR China.

出版信息

J Food Drug Anal. 2019 Jul;27(3):793-804. doi: 10.1016/j.jfda.2019.05.007. Epub 2019 Jun 26.

DOI:10.1016/j.jfda.2019.05.007
PMID:31324295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9307031/
Abstract

Jinzhen oral liquid (JZ) is a classical traditional Chinese medicine formula used for the treatment of children lung disease. However, the effective substance of JZ is still unclear. In this study, we used lung injury rat model to study the protective effect of JZ, through UPLC-Q-TOF/MS detection coupled with metabolic research and network pharmacology analysis. Fortunately, 31 absorbed prototype constituents and 41 metabolites were identified or tentatively characterized based on UPLC-Q-TOF/MS analysis, and the possible metabolic pathways were hydroxylation, sulfation and glucuronidation. We optimized the data screening in the early stage of network pharmacology by collecting targets based on adsorbed constituents, and further analyzed the main biological processes and pathways. 24 selected core targets were frequently involved in reactive oxygen species metabolic process, dopaminergic synapse pathway and so on, which might play important roles in the mechanisms of JZ for the treatment of lung injury. Overall, the absorbed constituents and their possible metabolic pathways, as well as the absorbed constituent-target-disease network provided insights into the mechanisms of JZ for the treatment of lung injury. Further studies are needed to validate the biological processes and effect pathways of JZ.

摘要

金振口服液(JZ)是一种经典的中药方剂,用于治疗儿童肺部疾病。然而,JZ 的有效物质仍不清楚。在这项研究中,我们使用肺损伤大鼠模型,通过 UPLC-Q-TOF/MS 检测结合代谢研究和网络药理学分析来研究 JZ 的保护作用。幸运的是,基于 UPLC-Q-TOF/MS 分析,鉴定或初步表征了 31 个吸收原型成分和 41 个代谢产物,可能的代谢途径为羟化、硫酸化和葡萄糖醛酸化。我们通过收集基于吸附成分的靶点,优化了网络药理学早期的数据筛选,并进一步分析了主要的生物学过程和途径。24 个选定的核心靶点经常参与活性氧代谢过程、多巴胺能突触途径等,这可能在 JZ 治疗肺损伤的机制中发挥重要作用。总的来说,吸收成分及其可能的代谢途径,以及吸收成分-靶点-疾病网络,为 JZ 治疗肺损伤的机制提供了深入的了解。需要进一步的研究来验证 JZ 的生物学过程和作用途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/a8e6c65339cd/jfda-27-03-793f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/dc2f9960fc17/jfda-27-03-793f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/d7d127e1f26f/jfda-27-03-793f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/492e12d8e287/jfda-27-03-793f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/a8e6c65339cd/jfda-27-03-793f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/dc2f9960fc17/jfda-27-03-793f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/d7d127e1f26f/jfda-27-03-793f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/492e12d8e287/jfda-27-03-793f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/9307031/a8e6c65339cd/jfda-27-03-793f4.jpg

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