Wang Yuming, Li Xue, Qi Min, Li Xiaokai, Zhang Fangfang, Wang Yuyu, Wu Junke, Shu Lexin, Fan Simiao, Li Yunfei, Li Yubo
School of Chinese Materia, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
TIPRHUYA Advancing Innovative Medicines Ltd., Tianjin, China.
Front Mol Biosci. 2023 Jun 23;10:1203208. doi: 10.3389/fmolb.2023.1203208. eCollection 2023.
YiYiFuZi powder (YYFZ) is a classical formula in Chinese medicine, which is commonly used clinically for the treatment of Chronic Heart Disease (CHD), but it's pharmacological effects and mechanism of action are currently unclear. An adriamycin-induced CHD model rat was established to evaluate the pharmacological effects of YYFZ on CHD by the results of inflammatory factor level, histopathology and echocardiography. Metabolomic studies were performed on rat plasma using UPLC-Q-TOF/MS to screen biomarkers and enrich metabolic pathways; network pharmacology analysis was also performed to obtain the potential targets and pathways of YYFZ for the treatment of CHD. The results showed that YYFZ significantly reduced the levels of TNF- and BNP in the serum of rats, alleviated the disorder of cardiomyocyte arrangement and inflammatory cell infiltration, and improved the cardiac function of rats with CHD. The metabolomic analysis identified a total of 19 metabolites, related to amino acid metabolism, fatty acid metabolism, and other metabolic pathways. Network pharmacology showed that YYFZ acts through PI3K/Akt signaling pathway, MAPK signaling pathway and Ras signaling pathway. YYFZ treatment of CHD modulates blood metabolic pattern and several protein phosphorylation cascades but importance specific changes for therapeutic effect require further studies.
益益附子散(YYFZ)是中医经典方剂,临床常用于治疗慢性心脏病(CHD),但其药理作用及作用机制目前尚不清楚。通过阿霉素诱导建立CHD模型大鼠,从炎症因子水平、组织病理学及超声心动图结果评估YYFZ对CHD的药理作用。采用超高效液相色谱-四级杆飞行时间质谱联用技术(UPLC-Q-TOF/MS)对大鼠血浆进行代谢组学研究,筛选生物标志物并富集代谢途径;同时进行网络药理学分析,以获得YYFZ治疗CHD的潜在靶点和途径。结果显示,YYFZ可显著降低大鼠血清中TNF-和BNP水平,减轻心肌细胞排列紊乱和炎性细胞浸润,改善CHD大鼠的心功能。代谢组学分析共鉴定出19种代谢物,涉及氨基酸代谢、脂肪酸代谢等代谢途径。网络药理学表明,YYFZ通过PI3K/Akt信号通路、MAPK信号通路和Ras信号通路发挥作用。YYFZ治疗CHD可调节血液代谢模式和多个蛋白磷酸化级联反应,但治疗效果的重要特异性变化仍需进一步研究。