Mass spectrum oriented metabolomics for evaluating the efficacy and discovering the mechanism of Shaofuzhuyu Decoction for endometriosis of cold coagulation and blood stasis

代谢组学 血瘀 计算生物学 小桶 子宫内膜异位症 汤剂 代谢途径 生物信息学 药理学 生物 医学 中医药 传统医学 生物化学 新陈代谢 内科学 基因本体论 病理 基因表达 替代医学 基因
作者
Fei Liu,Dongxia Yang,Sun Xiaolan,Saisai Yang,Yao Zhang,Qiyao Li,Siyao Deng,Hao‐Ran Dai,Xiuhong Wu
出处
期刊:Heliyon [Elsevier]
卷期号:10 (13): e33806-e33806
标识
DOI:10.1016/j.heliyon.2024.e33806
摘要

Shaofuzhuyu Decoction (SFZYD) is a classical formula for treating endometriosis of cold coagulation and blood stasis (ECB). The clinical efficacy is definite, but the potential mechanisms require further exploration. The study aimed to reveal the metabolic mechanisms of SFZYD for treating ECB using mass spectrum oriented metabolomics. Firstly, the study has used metabolomics data to identify biomarkers and to investigate metabolic pathways. Then, the targets of SFZYD for treating ECB were dug by building and analyzing a biological network of biomarkers. Finally, the obtained targets were validated by molecular docking. This study found that SFZYD could significantly improve the biochemical indicators and metabolic abnormalities of ECB. A total of 18 ECB-related biomarkers in 7 pathways were identified. SFZYD was able to regulate the levels of 14 biomarkers that were involved in 5 metabolic pathways. Furthermore, the study yielded 119 SFZYD active ingredients, 1119 target proteins associated with endometriosis, 610 targets associated with biomarkers, 727 GO functions, and 159 KEGG pathways. Biological network analysis constructed a network diagram of herbs-ingredients-targets-biomarkers, and found 6 key active ingredients and 9 core targets. Molecular docking showed high affinities between key ingredients and core targets. This study elucidated that SFZYD plays a role in treating ECB through multi-component, multi-target, and multi-pathway.
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