Chinese Journal of Pharmacovigilance ›› 2025, Vol. 22 ›› Issue (11): 1246-1252.
DOI: 10.19803/j.1672-8629.20250620

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Mechanisms of Anti-Myocardial Ischemia Reperfusion Injury of Qishen Yiqi Dropping Pills Based on UHPLC-MS/MS and Network Pharmacology

LIU Shuling1, JIANG Huiru1, CUI Herong2, ZHANG Zehan3, SHANG Hongcai1,4*   

  1. 1Beijing Key Laboratory of SMART Traditional Chinese Medicine for Chronic Disease Prevention and Treatment/Key Laboratory of Chinese Internal Medicine of Ministry of Education, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China;
    2School of Life Sciences, Beijing University of Chinese Medicine, Beijing 100029, China;
    3School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100105, China;
    4Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China
  • Received:2025-09-02 Online:2025-11-15 Published:2025-11-14

Abstract: Objective To identify the chemical constituents and blood-entering components of Qishen Yiqi dropping pills (QSYQ) using UHPLC-MS/MS, and to investigate its mechanism of action against myocardial ischemia-reperfusion injury (MIRI). Methods Chromatographic separation was performed on an ACQUITY UPLC HSS T3 column under gradient elution with a mobile phase consisting of 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (B). Data acquisition was conducted in both positive and negative ionization modes using a UPLC I-Class system coupled with a Synapt G2-Si Q-TOF mass spectrometer. Data processing was performed using the Unifi software's natural product workflow. A theoretical mass spectrometry database of 6400 natural products was used for identification of chemical constituents and blood-entering components. Potential targets of the identified blood-entering components and MIRI-related targets were retrieved from databases. Protein-protein interaction (PPI) networks were constructed to identify core targets of QSYQ against MIRI, followed by Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Results A total of 194 compounds were identified in QSYQ, while another 24 compounds were identified in the plasma of rats administered with QSYQ. The prototype components absorbed into the bloodstream included saponins and diterpenoid quinones. Network pharmacology analysis suggested that QSYQ exerted anti-MIRI effects by acting on key pathways such as the PI3K-AKT and HIF-1 signaling pathways. Conclusion The results of this study indicate that the prototype components absorbed into the bloodstream are likely the effective constituents of QSYQ. This research provides a reference for investigation into the pharmacodynamic material basis and pharmacological mechanisms of QSYQ.

Key words: Qishen Yiqi Dropping Pills, Blood-Entering Components, Saponins, Diterpenoid Quinones, Myocardial Ischemia-Reperfusion Injury, UHPLC-MS/MS, Rat, Network Pharmacology

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