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Serum proteomics study of Naoxintong Capsule against myocardial infarction
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DOI   10.11656/j.issn.1673-9043.2025.12.06
Key Words   Naoxintong Capsule;serum proteomics;myocardial infarction;angiogenesis;apoptosis
Author NameAffiliationE-mail
SHI Tingting School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
GENG Xiao School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
LI Mengyao School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
BAI Yuxin Instrumental Analysis and Research Center, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
WANG Hong School of Medical Technology, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China wanghongsys@126.com 
Abstract
    [Objective] To investigate the mechanism of Naoxintong capsule against myocardial infarction(MI) through serum proteomics. [Methods] MI was induced by ligating the left anterior descending coronary artery in C57BL/6 mice. Naoxintong[300 mg/(kg·d)]was administered for 3 days. Differentially expressed proteins(DEPs) were screened by two-dimensional gel electrophoresis(2-DE) and Matrix assisted Laser Desorption Ionization Time-Of-Flight Mass Spectrometry(MALDI-TOF-MS),validated by Western blot. Angiogenesis-related proteins were analyzed using proteomic arrays. [Results] Naoxintong reduced left ventricular infarct size and decreased cardiomyocyte apoptosis. Proteomic analysis identified 100 DEPs,including Vash1,Gpd1,Timp3,and Mfn1. Naoxintong upregulated PDGF-BB expression and activated the Akt/eNOS pathway. [Conclusion] Naoxintong exerts myocardial protective effects by synergistically regulating a triple network involving Vash1/PDGF-BB-mediated angiogenesis,TIMP3/MMP9-dominated matrix remodeling,and Mfn1-dependent mitochondrial dynamics.

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