基于超高效液相色谱-四极杆飞行时间串联质谱联用技术结合网络药理学探究四逆散抗抑郁作用机制:实验研究

Exploring the mechanism of Si-Ni-San against depression by UPLC-Q-TOF-MS/MS integrated with network pharmacology: experimental research.

作者信息

Jia Keke, Li Changyin, Xu Meijuan, Dai Guoliang, Zhou Jinyong, Chen Biqing, Zou Jiandong, Li Jia, Zhang Qingyu, Ju Wenzheng

机构信息

School of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine.

Department of Clinical Pharmacology.

出版信息

Ann Med Surg (Lond). 2023 Nov 7;86(1):172-189. doi: 10.1097/MS9.0000000000001464. eCollection 2024 Jan.

Abstract

BACKGROUND

Depression is becoming an urgent mental health problem. Si-Ni-San has been widely used to treat depression, yet its underlying pharmacological mechanism is poorly understood. Thus, we aim to explore the antidepressant mechanism of Si-Ni-San by chemical analysis and in-silico methods.

METHODS

Compounds in Si-Ni-San were determined by ultra-high performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS/MS). Then, bioactive compounds were obtained from Traditional Chinese Medicines for Systems Pharmacology Database and Analysis Platform and SwissADME, and the potential targets of which were acquired from SwissTargetPrediction. Depression-related targets were collected from GeneCards. The intersection between compound-related targets and depression-related targets were screened out, and the overlapped targets were further performed protein-protein interaction, biological functional and pathway enrichment analysis. Finally, networks of Si-Ni-San against depression were constructed and visualized by Cytoscape.

RESULTS

One hundred nineteen compounds in Si-Ni-San were determined, of which 24 bioactive compounds were obtained. Then, 137 overlapped targets of Si-Ni-San against depression were collected. AKT1, PIK3R1, PIK3CA, mTOR, MAPK1 and MAPK8 were the key targets. Furthermore, PI3K-Akt signalling pathway, serotonergic synapse, MAPK signalling pathway and neurotrophin signalling pathway were involved in the antidepressant mechanism of Si-Ni-San. It showed that components like sinensetin, hesperetin, liquiritigenin, naringenin, quercetin, albiflorin and paeoniflorin were the mainly key active compounds for the antidepressant effect of Si-Ni-San.

CONCLUSIONS

This study demonstrated the key components, key targets and potential pharmacological mechanisms of Si-Ni-San against depression. These results indicate that Si-Ni-San is a promising therapeutic approach for treatment of depression, and may provide evidence for the research and development of drugs for treating depression.

摘要

背景

抑郁症正成为一个紧迫的心理健康问题。四逆散已被广泛用于治疗抑郁症,但其潜在的药理机制尚不清楚。因此,我们旨在通过化学分析和计算机模拟方法探索四逆散的抗抑郁机制。

方法

采用超高效液相色谱-四极杆飞行时间串联质谱联用技术(UPLC-Q-TOF-MS/MS)测定四逆散中的化合物。然后,从中药系统药理学数据库与分析平台和瑞士药物数据库中获取生物活性化合物,并从瑞士靶点预测数据库中获取其潜在靶点。从基因卡片数据库收集抑郁症相关靶点。筛选化合物相关靶点与抑郁症相关靶点的交集,并对重叠靶点进行蛋白质-蛋白质相互作用、生物学功能和通路富集分析。最后,用Cytoscape构建并可视化四逆散抗抑郁网络。

结果

确定了四逆散中的119种化合物,其中获得了24种生物活性化合物。然后,收集了四逆散抗抑郁的137个重叠靶点。AKT1、PIK3R1、PIK3CA、mTOR、MAPK1和MAPK8是关键靶点。此外,PI3K-Akt信号通路、5-羟色胺能突触、MAPK信号通路和神经营养因子信号通路参与了四逆散的抗抑郁机制。结果表明,橙皮素、橙皮苷、甘草素、柚皮苷、槲皮素、白花芍药苷和芍药苷等成分是四逆散抗抑郁作用的主要关键活性化合物。

结论

本研究阐明了四逆散抗抑郁的关键成分、关键靶点及潜在药理机制。这些结果表明,四逆散是一种有前途的抑郁症治疗方法,可能为抑郁症治疗药物的研发提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e246/10783272/400d95f1ad7f/ms9-86-172-g001.jpg

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