Han Jiajun, Miao Yuyang, Song Linze, Zhou Xianfeng, Liu Yan, Wang Lin, Zhu Kai, Ma He, Ma Yan, Li Qingjie, Han Dong
College of Pharmacy, Changchun University of Chinese Medicine, Jilin, China.
Department of Endocrinology and Metabolism, Jilin Province People's Hospital, Jilin, China.
FASEB J. 2025 Jan 31;39(2):e70363. doi: 10.1096/fj.202402688R.
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.
血府逐瘀汤(XZD)广泛应用于心血管疾病的治疗。本研究旨在探讨血府逐瘀汤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依据。本研究通过网络药理学预测血府逐瘀汤改善高脂血症所调控的信号通路。采用分子对接技术验证血府逐瘀汤中各成分与靶点之间的亲和力。此外,通过高脂饮食构建大鼠高脂血症模型。通过组织病理学染色、酶联免疫吸附测定(ELISA)和蛋白质免疫印迹法(western blot)验证血府逐瘀汤对高脂血症的影响。结果发现,血府逐瘀汤改善了高脂血症大鼠的血脂异常和炎症因子紊乱,抑制了肝功能损害、病理损伤和氧化应激损伤。分子对接和网络药理学研究结果表明,血府逐瘀汤改善高脂血症的机制可能与丝裂原活化蛋白激酶(MAPK)、核因子κB(NF-κB)和过氧化物酶体增殖物激活受体(PPAR)信号通路密切相关。本研究表明,血府逐瘀汤通过调节MAPK/NF-κB和MAPK/PPARα/肉碱/有机阳离子转运体1A(CPT-1A)信号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,对高脂血症大鼠起到保护作用。