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养神定志颗粒的抗焦虑作用:整合网络药理学与海马代谢组学

Anxiolytic effect of YangshenDingzhi granules: Integrated network pharmacology and hippocampal metabolomics.

作者信息

Lv Shimeng, Dai Weibo, Zheng Yan, Dong Ping, Yu Yihong, Zhao Yifan, Sun Shiguang, Bi Dezhong, Liu Chuanguo, Han Fabin, Wu Jibiao, Zhao Tingting, Ma Yuexiang, Zheng Feng, Sun Peng

机构信息

School of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, China.

Department of Pharmacy, Zhongshan Hospital of Traditional Chinese Medicine, Zhong Shan, China.

出版信息

Front Pharmacol. 2022 Oct 31;13:966218. doi: 10.3389/fphar.2022.966218. eCollection 2022.

Abstract

Anxiety disorder is one of the most common mental diseases. It is mainly characterized by a sudden, recurring but indescribable panic, fear, tension and/or anxiety. Yangshendingzhi granules (YSDZ) are widely used in the treatment of anxiety disorders, but its active ingredients and underlying mechanisms are not yet clear. This study integrates network pharmacology and metabolomics to investigate the potential mechanism of action of YSDZ in a rat model of anxiety. First, potential active ingredients and targets were screened by network pharmacology. Then, predictions were verified by molecular docking, molecular dynamics and western blotting. Metabolomics was used to identify differential metabolites and metabolic pathways. All results were integrated for a comprehensive analysis. Network pharmacology analysis found that Carotene, β-sitosterol, quercetin, Stigmasterol, and kaempferol in YSDZ exert anxiolytic effects mainly by acting on IL1β, GABRA1, PTGS1, ESR1, and TNF targets. Molecular docking results showed that all the affinities were lower than -5 kcal/mol, and the average affinities were -7.7764 kcal/mol. Molecular dynamics simulation results showed that RMSD was lower than 2.5 A, and the overall conformational changes of proteins were small, indicating that the small molecules formed stable complexes with proteins. The results of animal experiments showed that YSDZ exerts anxiolytic effects by regulating GABRA1 and TNF-α, ameliorating pathological damage in hippocampal CA1, and regulating metabolic pathways such as thiamine, cysteine and methionine metabolism, lysine biosynthesis and degradation. Altogether, we reveal multiple mechanisms through which YSDZ exerts its anti-anxiety effects, which may provide a reference for its clinical application and drug development.

摘要

焦虑症是最常见的精神疾病之一。其主要特征为突然出现、反复发生但难以描述的恐慌、恐惧、紧张和/或焦虑。养神定志颗粒(YSDZ)被广泛用于治疗焦虑症,但其活性成分和潜在机制尚不清楚。本研究整合网络药理学和代谢组学,以研究YSDZ在大鼠焦虑模型中的潜在作用机制。首先,通过网络药理学筛选潜在的活性成分和靶点。然后,通过分子对接、分子动力学和蛋白质印迹法验证预测结果。代谢组学用于鉴定差异代谢物和代谢途径。综合所有结果进行全面分析。网络药理学分析发现,YSDZ中的胡萝卜素、β-谷甾醇、槲皮素、豆甾醇和山奈酚主要通过作用于IL1β、GABRA1、PTGS1、ESR1和TNF靶点发挥抗焦虑作用。分子对接结果显示,所有亲和力均低于-5 kcal/mol,平均亲和力为-7.7764 kcal/mol。分子动力学模拟结果显示,RMSD低于2.5 Å,蛋白质的整体构象变化较小,表明小分子与蛋白质形成了稳定的复合物。动物实验结果表明,YSDZ通过调节GABRA1和TNF-α发挥抗焦虑作用,改善海马CA1区的病理损伤,并调节硫胺素、半胱氨酸和蛋氨酸代谢、赖氨酸生物合成和降解等代谢途径。总之,我们揭示了YSDZ发挥抗焦虑作用的多种机制,这可能为其临床应用和药物开发提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcf8/9659911/c9f9f8ae1256/fphar-13-966218-g001.jpg

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