Key result
Baihe Dihuang-Danshen Decoction reduces myocardial structural damage and suppresses MIRI-induced target mRNA upregulation in rats.
Why the study?
Myocardial ischemia-reperfusion injury impairs cardiac surgery prognosis, and the core compounds and mechanisms of Baihe Dihuang-Danshen Decoction remained to be identified.
Does Baihe Dihuang-Danshen Decoction reduce myocardial ischemia-reperfusion injury in preclinical models?
Does Baihe Dihuang-Danshen Decoction reduce myocardial ischemia-reperfusion injury in preclinical models?
Answers are grounded in this paper and cite their sources.
Baihe Dihuang-Danshen Decoction demonstrates cardioprotective effects against myocardial ischemia-reperfusion injury in preclinical models through multi-target modulation.
Introduction: Myocardial ischemia-reperfusion injury (MIRI) significantly impairs the prognosis of cardiac surgery. Baihe Dihuang-Danshen Decoction (BDDSD), a Chinese herbal formula, has shown efficacy against MIRI. This study combined network pharmacology and experimental validation to identify the core compounds and mechanisms of BDDSD. Methods: The compounds of BDDSD were identified through the TCMSP and BATMAN databases. Potential targets were determined by intersecting MIRI-related differential genes with BDDSD compound targets. A protein-protein interaction (PPI) network was constructed using the STING platform. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were performed using the Metascape database. A TF-gene network and a gene-miRNA network were generated using the NetworkAnalyst platform. Immune infiltration analysis was conducted using CIBERSORT. In vivo verification was then performed, followed by molecular docking analysis. Results: The analysis revealed that BDDSD's cardioprotective effects against MIRI are mediated by six core compounds (e.g., Tanshinone IIA, Cryptotanshinone), which synergistically modulate key targets (e.g., IL6, HMOX1). In rats, BDDSD treatment reduced myocardial structural damage. Notably, MIRI-induced upregulation of mRNA expression of all six core targets was significantly suppressed by BDDSD. Molecular docking confirmed strong compound-target binding, further validating BDDSD's efficacy in MIRI. Discussion: Our study elucidated the mechanisms underlying BDDSD's action in MIRI treatment. However, given that BDDSD operates through multiple components and targets, the complex interactions between these compounds require further investigation. Additionally, comprehensive toxicity assessments in preclinical models are needed to establish its safety profile. Conclusion: This study provides a comprehensive overview of the core compounds, potential targets, and mechanisms of BDDSD in MIRI treatment, offering a foundation for further research into the pathological mechanisms of MIRI and the therapeutic potential of traditional Chinese herbal decoctions.
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Huang et al. (2026) studied Myocardial ischemia-reperfusion injury (MIRI). Baihe Dihuang-Danshen Decoction (BDDSD) was evaluated on Myocardial structural damage and mRNA expression of core targets. Baihe Dihuang-Danshen Decoction reduced myocardial structural damage and significantly suppressed MIRI-induced upregulation of mRNA expression of six core targets in rats.
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