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基于质谱的代谢组学用于评估少腹逐瘀汤治疗寒凝血瘀型子宫内膜异位症的疗效及探索其作用机制

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

作者信息

Liu Jing, Yang Dongxia, Sun Xiaolan, Yang Saisai, Zhang Yao, Li Qiyao, Deng Siyao, Dai Haoran, Wu Xiuhong

机构信息

School of Pharmacy, Heilongjiang University of Chinese Medicine, Harbin, China.

Department of Gynecology Medicine, Second Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, China.

出版信息

Heliyon. 2024 Jul 2;10(13):e33806. doi: 10.1016/j.heliyon.2024.e33806. eCollection 2024 Jul 15.

Abstract

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.

摘要

少腹逐瘀汤是治疗寒凝血瘀型子宫内膜异位症的经典方剂。临床疗效确切,但潜在机制有待进一步探索。本研究旨在采用质谱导向代谢组学揭示少腹逐瘀汤治疗寒凝血瘀型子宫内膜异位症的代谢机制。首先,利用代谢组学数据鉴定生物标志物并研究代谢途径。然后,通过构建和分析生物标志物的生物网络挖掘少腹逐瘀汤治疗寒凝血瘀型子宫内膜异位症的靶点。最后,通过分子对接验证所获得的靶点。本研究发现少腹逐瘀汤可显著改善寒凝血瘀型子宫内膜异位症的生化指标和代谢异常。共鉴定出7条途径中的18个与寒凝血瘀型子宫内膜异位症相关的生物标志物。少腹逐瘀汤能够调节参与5条代谢途径的14个生物标志物的水平。此外,本研究还得到了119种少腹逐瘀汤活性成分、1119个与子宫内膜异位症相关的靶蛋白、610个与生物标志物相关的靶点、727个基因本体功能和159条京都基因与基因组百科全书途径。生物网络分析构建了草药-成分-靶点-生物标志物网络图,发现了6种关键活性成分和9个核心靶点。分子对接显示关键成分与核心靶点之间具有高亲和力。本研究阐明少腹逐瘀汤通过多成分、多靶点、多途径发挥治疗寒凝血瘀型子宫内膜异位症的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58c2/11279264/ec524374563f/ga1.jpg

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