Integration of LC-LTQ-Orbitrap-MS and Network Pharmacology to Analyzethe Active Components of Sijunzi Decoction and their Mechanism ofAction Against Cytotoxicity-associated Premature Ovarian Insufficiency

小桶 卵巢早衰 计算生物学 ErbB公司 机制(生物学) MAPK/ERK通路 作用机理 PI3K/AKT/mTOR通路 生物 药理学 信号转导 医学 基因 生物化学 基因本体论 基因表达 哲学 认识论 体外 内科学
作者
Yiying Chen,Sixuan Han,Kang An,Rui Fu,Li Chen,Jinrui Guo,Qiong Wang
出处
期刊:Combinatorial Chemistry & High Throughput Screening [Bentham Science Publishers]
卷期号:26 (14): 2437-2451 被引量:4
标识
DOI:10.2174/1386207326666230303094247
摘要

INTRODUCTION: Sijunzi Decoction (SJZD) is a classical prescription in traditional Chinese medicine that enhances neuroimmune endocrine function to alleviate inflammatory aging, a key pathogenic mechanism underlying premature ovarian insufficiency (POI). However, the mechanism through which SJZD alleviates POI remains unknown. Hence, we aimed to identify the active components of SJZD and its mechanism of therapeutic action against POI. METHODS: We identified compounds in SJZD using liquid chromatography-linear trap quadrupole- Orbitrap-mass spectrometry (LC-LTQ-Orbitrap-MS). Traditional Chinese Medicine Systems (TCMSP) and HERB databases were used to identify the ingredients and potential targets of SJZD. We analyzed Gene Ontology (GO) terms and enriched Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways using RStudio and constructed a visual network using Cytoscape3.9.1. RESULTS: We identified 98 compounds using LC-LTQ-Orbitrap-MS, among which 29 were bioactive. The screen outputted yielded 151 predicted targets of these compounds that were associated with POI. The results of the GO and KEGG analyses showed that these compounds play key roles in cell growth, division, migration, and survival signaling pathways. Therefore, phosphatidylinositol 3-kinase (PI3K)/AKT, mitogen-activated protein kinase (MAPK), and epidermal growth factor receptor (EGFR) pathways might be closely associated with the pharmacological effects of SJZD on the pathological processes of POI. CONCLUSION: Our findings provide a scientific basis for rapidly analyzing bioactive compounds in SJZD and their pharmacological mechanisms.
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