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基于化学图谱、网络药理学及实验验证的胡杨养坤方治疗卵巢早衰的活性成分及作用机制研究

Study on the active ingredients and mechanism of Huyang Yangkun Formula for treating premature ovarian insufficiency via chemical profiling, network pharmacology, and experimental validation.

作者信息

Li Yang, Zeng Liuxi, Peng Yin, Liu Jian, Li Xiong, Yang Hongyan

机构信息

The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510120, China; Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, China.

School of Traditional Chinese Medicine, Shenyang Pharmaceutical University, Bengxi, liaoning 117000, China.

出版信息

J Pharm Biomed Anal. 2025 Sep 15;263:116951. doi: 10.1016/j.jpba.2025.116951. Epub 2025 May 8.

Abstract

Huyang Yangkun Formula (HYF) is a Chinese herbal remedy used for premature ovarian insufficiency (POI), though its active ingredients and mechanisms are not well understood.This study aims to identify HYF's chemical components and investigate its mechanism in treating POI. Using UHPLC-QE Focus HRMS, chemical profiling and quantification were conducted. The therapeutic effects and target validation of HYF were examined using a POI rat model, human ovarian granulosa cells (COV434), and network pharmacology. Molecular docking was used to predict the affinity of active compounds for the key target TP53. 125 compounds were identified in HYF, including flavonoids, organic acids, saponins and phenylethanoid glycosides. By using network pharmacological analysis, a total of 123 potential targets for the HYF treatment of POI were identified. PIK3R1, AKT1, EGFR, MMP2 and TP53 were deduced to be core targets of HYF for treating POI, and the main pathway included HIF-1, PI3K-Akt and P53 signaling pathway. HYF enhances follicle development and ovarian function by reducing apoptosis in ovarian granulosa cells in VCD-POI rats. In vitro, HYF decreased VCD-induced COV434 cell death. qRT-PCR and WB experiments identified the P53-mitochondrial apoptosis signaling pathway as the main target, with molecular docking showing Hyperoside, Isochlorogenic acid B, and Baohuoside I having the highest binding affinity to TP53.The potential active components and mechanisms of HYF in relation to POI were investigated through chemical profiling, network pharmacology, and both in vitro and in vivo experimental validation.

摘要

胡杨养坤方(HYF)是一种用于治疗卵巢早衰(POI)的中药方剂,但其活性成分和作用机制尚不清楚。本研究旨在确定HYF的化学成分,并研究其治疗POI的机制。采用超高效液相色谱-四极杆飞行时间高分辨质谱(UHPLC-QE Focus HRMS)进行化学图谱分析和定量分析。使用POI大鼠模型、人卵巢颗粒细胞(COV434)和网络药理学研究了HYF的治疗效果和靶点验证。采用分子对接预测活性化合物与关键靶点TP53的亲和力。在HYF中鉴定出125种化合物,包括黄酮类、有机酸、皂苷和苯乙醇苷。通过网络药理学分析,共鉴定出123个HYF治疗POI的潜在靶点。推断PIK3R1、AKT1、EGFR、MMP2和TP53是HYF治疗POI的核心靶点,主要信号通路包括HIF-1、PI3K-Akt和P53信号通路。HYF通过减少VCD-POI大鼠卵巢颗粒细胞的凋亡来促进卵泡发育和卵巢功能。在体外,HYF可减少VCD诱导的COV434细胞死亡。qRT-PCR和WB实验确定P53-线粒体凋亡信号通路为主要靶点,分子对接显示金丝桃苷、异绿原酸B和宝藿苷I与TP53的结合亲和力最高。通过化学图谱分析、网络药理学以及体外和体内实验验证,研究了HYF治疗POI的潜在活性成分和机制。

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