化学
机制(生物学)
心肌梗塞
药理学
钙
医学
系统药理学
信号转导
心脏病学
药品
内科学
生物化学
认识论
哲学
作者
Siyu Guo,Yingying Tan,Zhihong Huang,Yikui Li,Weiyu Liu,Xiaotian Fan,Jingyuan Zhang,Antony Stalin,Changgeng Fu,Zhishan Wu,Penglong Wang,Wei Zhou,Xinkui Liu,Chao Wu,Shanshan Jia,Jinyan Zhang,Xiaoxia Duan,Jiarui Wu
标识
DOI:10.3389/fphar.2022.839936
摘要
Introduction: Danhong injection (DHI) is a traditional Chinese medicine preparation commonly used in the clinical treatment of acute myocardial infarction (AMI). In this study, the active components of DHI and its mechanism in the treatment of AMI were investigated. Methods: The chemical components of DHI were detected by the ultra-high-performance liquid chromatography-linear trap quadrupole-orbitrap-tandem mass spectrometry (UHPLC-LTQ-Orbitrap-MS/MS), and the targets and pathways of DHI in the treatment of AMI were analyzed by systems pharmacology, which was verified by molecular docking and animal experiments. Results: A total of 12 active components of DHI were obtained, and 158 common targets of component and disease were identified by systems pharmacology. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis results showed that DHI is closely related to the calcium signaling pathway in the treatment of AMI. Molecular docking showed that the key target protein has good binding affinity to related compounds. The experimental results showed that compared with the model group, LVAWs, EF, and FS significantly ( p < 0.05) increased in the DHI group. The percentage of myocardial infarction significantly ( p < 0.01) decreased, both in the ventricular and total cardiac regions, and the pathological damage of myocardial tissue also decreased. In addition, the expression of the protein CaMK II decreased ( p < 0.01) and the expression of SERCA significantly increased ( p < 0.01). Conclusion: This study revealed that ferulic acid, caffeic acid and rosmarinic acid could inhibit AMI by regulating PLB, CaMK II, SERCA, etc. And mechanistically, calcium signaling pathway was critically involved. Combination of systems pharmacology prediction with experimental validation may provide a scientific basis for in-depth clinical investigation of the material basis of DHI.
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