Investigating the anti-atherosclerotic effects and potential mechanism of Dalbergia odorifera in ApoE-deficient mice using network pharmacology combined with metabolomics

被引:0
|
作者
Sun, Kang [1 ]
Li, Zongchao [1 ]
Li, Wenjing [1 ]
Chi, Chenglin [1 ]
Wang, Minjun [1 ]
Xu, Ruoxuan [1 ]
Gao, Yan [2 ]
Li, Bing [2 ]
Sun, Yiying [2 ]
Liu, Rongxia [1 ]
机构
[1] Yantai Univ, Sch Pharm, Minist Educ, Collaborat Innovat Ctr Adv Drug Delivery Syst & Bi, Yantai, Peoples R China
[2] Shandong Int Biotechnol Pk Dev Co Ltd, Yantai, Peoples R China
基金
中国国家自然科学基金;
关键词
Atherosclerosis; Dalbergia odorifera; Metabolomics; Network pharmacology; Vascular smooth muscle cells; SMOOTH-MUSCLE-CELLS; KAPPA-B; EXPRESSION; PROTEIN; PROLIFERATION; INHIBITION; PACLITAXEL; GLUTAMATE; SYNTHASE; KINASE;
D O I
10.1016/j.jpba.2024.116017
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Dalbergia odorifera (DO) is a precious rosewood species in Southern Asia, and its heartwood is used in China as an official plant for invigorating blood circulation and eliminating stasis. This study aims to evaluate the efficacy of DO on atherosclerosis (AS), and further explore its active components and potential mechanisms. The apolipoprotein-E (ApoE)-deficient mice fed a high-fat diet were used as model animals, and the pathological changes in mice with or without DO treatment were compared to evaluate the pharmacodynamics of DO on AS. The mechanisms were preliminarily expounded by combining with metabolomics and network pharmacology. Moreover, the bioactive components and targets were assessed by cell experiments and molecular docking, respectively. Our findings suggested that DO significantly modulated blood lipid levels and alleviated intimal hyperplasia in atherosclerotic-lesioned mice, and the mechanisms may involve the regulation of 18 metabolites that changed during the progression of AS, thus affecting 3 major metabolic pathways and 3 major signaling pathways. Moreover, the interactions between 16 compounds with anti-proliferative effect and hub targets in the 3 signaling pathways were verified using molecular docking. Collectively, our findings preliminarily support the therapeutic effect of DO in atherosclerosis, meanwhile explore the active constituents and potential pharmacological mechanisms, which is conducive to its reasonable exploitation and utilization.
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页数:12
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