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通过网络药理学及HPLC-Q-TOF-MS/MS分析在小鼠实验性变应性鼻炎模型和分离的嗜碱性白血病细胞系RBL-2H3中鉴定中药玉屏风散的活性标志物

Identification of Active Markers of Chinese Formula Yupingfeng San by Network Pharmacology and HPLC-Q-TOF-MS/MS Analysis in Experimental Allergic Rhinitis Models of Mice and Isolated Basophilic Leukemia Cell Line RBL-2H3.

作者信息

Li Xinqi, Zhao Caining, Qi Jin

机构信息

Research Center for Traceability and Standardization of TCMs, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China.

出版信息

Pharmaceuticals (Basel). 2025 Apr 7;18(4):540. doi: 10.3390/ph18040540.

Abstract

Yupingfeng San (YPFS) is a classic formula for treating allergic rhinitis (AR), which is composed of Bunge (AST), Koidz (AMR), and (Turcz.) Schischk (SR) at a ratio of 3:1:1. However, the potential bioactive components of YPFS relevant to AR treatment are currently unknown. This study combined in vivo chemical profiling, network pharmacology, and experimental validation to identify the substances in YPFS that are active against AR. Firstly, 98 compounds in YPFS were identified using high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (HPLC-Q-TOF-MS/MS) with the assistance of Global Natural Products Social (GNPS) molecular networking. Then, 42 prototype components and 57 metabolites were detected in the plasma, urine, and feces of mice with AR. A network pharmacological analysis based on 42 in vivo prototypical components was also conducted to screen 15 key components and 10 core targets, and 6 key components were further selected through molecular docking. Finally, the four key active components (cimifugin, wogonin, formononetin, and atractylenolide I) were revealed to be the main ingredients of YPFS through validation (in vitro and in vivo). This is the first systematic study of the components of YPFS in AR mice, laying the foundation for elucidating the overall material basis of this formulation. This study provides rich basic data for further pharmacological and mechanistic studies on YPFS.

摘要

玉屏风散(YPFS)是治疗变应性鼻炎(AR)的经典方剂,由防风(AST)、黄芪(AMR)和白术(SR)按3:1:1的比例组成。然而,目前尚不清楚YPFS中与AR治疗相关的潜在生物活性成分。本研究结合体内化学图谱分析、网络药理学和实验验证,以确定YPFS中对AR有活性的物质。首先,借助全球天然产物社会(GNPS)分子网络,采用高效液相色谱-四极杆飞行时间质谱(HPLC-Q-TOF-MS/MS)鉴定了YPFS中的98种化合物。然后,在AR小鼠的血浆、尿液和粪便中检测到42种原型成分和57种代谢产物。还基于42种体内原型成分进行了网络药理学分析,以筛选出15种关键成分和10个核心靶点,并通过分子对接进一步选择了6种关键成分。最后,通过验证(体外和体内)揭示了四种关键活性成分(升麻素苷、汉黄芩素、芒柄花素和白术内酯I)是YPFS的主要成分。这是首次对AR小鼠中YPFS的成分进行系统研究,为阐明该方剂的整体物质基础奠定了基础。本研究为进一步开展YPFS的药理学和作用机制研究提供了丰富的基础数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfb8/12030416/36ff82de32ed/pharmaceuticals-18-00540-g001.jpg

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