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

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 co...

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Autores principales: Guo, Jing-Yan, Wang, Dong-Mei, Wang, Meng-Jiao, Zhou, Jun, Pan, Ying-Ni, Wang, Zheng-Zhong, Xiao, Wei, Liu, Xiao-Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307031/
https://www.ncbi.nlm.nih.gov/pubmed/31324295
http://dx.doi.org/10.1016/j.jfda.2019.05.007
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author Guo, Jing-Yan
Wang, Dong-Mei
Wang, Meng-Jiao
Zhou, Jun
Pan, Ying-Ni
Wang, Zheng-Zhong
Xiao, Wei
Liu, Xiao-Qiu
author_facet Guo, Jing-Yan
Wang, Dong-Mei
Wang, Meng-Jiao
Zhou, Jun
Pan, Ying-Ni
Wang, Zheng-Zhong
Xiao, Wei
Liu, Xiao-Qiu
author_sort Guo, Jing-Yan
collection PubMed
description 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.
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spelling pubmed-93070312022-08-09 Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis Guo, Jing-Yan Wang, Dong-Mei Wang, Meng-Jiao Zhou, Jun Pan, Ying-Ni Wang, Zheng-Zhong Xiao, Wei Liu, Xiao-Qiu J Food Drug Anal Original Article 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. Taiwan Food and Drug Administration 2019-06-26 /pmc/articles/PMC9307031/ /pubmed/31324295 http://dx.doi.org/10.1016/j.jfda.2019.05.007 Text en © 2019 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Guo, Jing-Yan
Wang, Dong-Mei
Wang, Meng-Jiao
Zhou, Jun
Pan, Ying-Ni
Wang, Zheng-Zhong
Xiao, Wei
Liu, Xiao-Qiu
Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title_full Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title_fullStr Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title_full_unstemmed Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title_short Systematically characterize the substance basis of Jinzhen oral liquid and their pharmacological mechanism using UPLC-Q-TOF/MS combined with network pharmacology analysis
title_sort systematically characterize the substance basis of jinzhen oral liquid and their pharmacological mechanism using uplc-q-tof/ms combined with network pharmacology analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307031/
https://www.ncbi.nlm.nih.gov/pubmed/31324295
http://dx.doi.org/10.1016/j.jfda.2019.05.007
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