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质谱分析与生物信息学分析相结合用于表征红景天抗炎活性成分及其作用靶点

Combination of mass spectrometry analysis and bioinformatic analysis for characterizing anti-inflammation active components from Boschniakia rossica and the targets.

作者信息

Hu Tingting, Li Maocheng, Zhang Xinyue, Gao Yuqian, Gao Hang, Liu Luyao, Zuo Along, Wang Yuling, Guo Jianpeng, Zheng Yan

机构信息

Key Laboratory of Natural Medicines of the Changbai Mountain, Ministry of Education, College of Pharmacy, Yanbian University, Yanji, Jilin Province, 133002, China.

School of Pharmaceutical Sciences, Jilin University, Changchun, Jilin Province, 130015, China.

出版信息

J Chromatogr A. 2025 Jan 4;1739:465544. doi: 10.1016/j.chroma.2024.465544. Epub 2024 Nov 22.

DOI:10.1016/j.chroma.2024.465544
PMID:39608234
Abstract

Alzheimer's disease (AD), a demonstrativeness disease with insidious onset, has become an important public health problem worldwide and is the fifth leading cause of death in the world. Boschniakia rossica (BR) has been used to treat age-related diseases, especially AD in China for centuries, but the material basis and mechanism are unclear. Here, we investigated the effective components and the mechanism of BR in the treatment of AD. The therapeutic effect of BR was verified through pathological and behavioral studies of AD rat model. BR can significantly increase the number of nerve cells in the hippocampus and improve the study and memory ability of AD rats. Subsequently, the active composition and the potential targets of BR were explored by UPLC-Q-Orbitrap-HRMS and network pharmacology. Ursolic acid, baicalein, and salicylic acid were the potential pharmacodynamic components acted on the phosphatidylinositol 3-kinase (PI3 K)/protein kinase B (AKT) pathway, which was verified by further molecular docking and molecular dynamics simulations. The in vivo and in vitro study revealed that BR treat AD by reducing the neurotoxicity of Aβ induced nerve cells by regulating PI3K/AKT signaling pathway. Our data strongly support a theoretical basis and methodology for the treatment of AD by BR and a reference for its new drug development.

摘要

阿尔茨海默病(AD)是一种起病隐匿的神经退行性疾病,已成为全球重要的公共卫生问题,是全球第五大死因。数百年来,草苁蓉在中国一直被用于治疗与年龄相关的疾病,尤其是AD,但物质基础和作用机制尚不清楚。在此,我们研究了草苁蓉治疗AD的有效成分及其作用机制。通过AD大鼠模型的病理和行为学研究验证了草苁蓉的治疗效果。草苁蓉可显著增加海马区神经细胞数量,提高AD大鼠的学习和记忆能力。随后,采用超高效液相色谱-四极杆-轨道阱-高分辨质谱(UPLC-Q-Orbitrap-HRMS)和网络药理学方法探索了草苁蓉的活性成分和潜在靶点。熊果酸、黄芩素和水杨酸是作用于磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(AKT)通路的潜在药效成分,这通过进一步的分子对接和分子动力学模拟得到了验证。体内和体外研究表明,草苁蓉通过调节PI3K/AKT信号通路降低Aβ诱导的神经细胞神经毒性来治疗AD。我们的数据有力地支持了草苁蓉治疗AD的理论基础和方法,并为其新药开发提供了参考。

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