Xuefu Zhuyu Decoction improves hyperlipidemia through the MAPK/NF-κB and MAPK/PPARα/CPT-1A signaling pathway

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY The FASEB Journal Pub Date : 2025-01-29 DOI:10.1096/fj.202402688R
Jiajun Han, Yuyang Miao, Linze Song, Xianfeng Zhou, Yan Liu, Lin Wang, Kai Zhu, He Ma, Yan Ma, Qingjie Li, Dong Han
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Abstract

Xuefu Zhuyu Decoction (XZD) is widely used in the treatment of cardiovascular diseases. The purpose of this study was to explore the pharmacological effects and molecular mechanisms of XZD in improving hyperlipidemia and to provide a theoretical framework for clinical application. In this study, the signaling pathways regulated by XZD in improving hyperlipidemia were predicted by network pharmacology. Molecular docking was used to verify the affinity between the components in XZD and the target. Furthermore, a hyperlipidemic model in rats was constructed through feeding a high-fat diet. The effect of XZD on hyperlipidemia was verified by histopathological staining, Elisa, and western blot. The results found that the XZD improved dyslipidemia and inflammatory factor disorders, and inhibited liver function damage, pathological damage, and oxidative stress damage in hyperlipidemic rats. The findings from molecular docking and network pharmacology suggested that the mechanism of XZD improving hyperlipidemia may be closely related to the MAPK, NF-κB, and PPAR pathways. This study demonstrated that the XZD inhibited liver lipid metabolism disorder and inflammatory response by regulating the MAPK/NF-κB and MAPK/PPARα/CPT-1A pathway, significantly improved liver histopathological damage and oxidative stress injury, and played a protective role in hyperlipidemic rats.

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血虚助瘀汤通过MAPK/NF-κB和MAPK/PPARα/CPT-1A信号通路改善高脂血症。
血瘀逐瘀汤被广泛用于治疗心血管疾病。本研究旨在探讨XZD改善高脂血症的药理作用及分子机制,为临床应用提供理论框架。本研究通过网络药理学方法预测XZD改善高脂血症的信号通路。通过分子对接验证XZD中各组分与靶标之间的亲和力。并通过高脂饮食建立大鼠高脂血症模型。通过组织病理学染色、酶联免疫吸附和western blot验证XZD对高脂血症的影响。结果发现,XZD能改善高脂血症大鼠血脂异常和炎症因子紊乱,抑制肝功能损害、病理损害和氧化应激损伤。分子对接和网络药理学结果提示XZD改善高脂血症的机制可能与MAPK、NF-κB、PPAR通路密切相关。本研究表明XZD通过调节MAPK/NF-κB和MAPK/PPARα/CPT-1A通路抑制肝脏脂质代谢紊乱和炎症反应,显著改善肝脏组织病理学损伤和氧化应激损伤,对高脂血症大鼠具有保护作用。
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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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