Key result
Shenqi Fuzheng formula outperforms single herbs to reduce AMI infarct size via enhanced angiogenesis.
Why the study?
The molecular basis of the synergistic cardio-protective effects of Codonopsis Radix and Astragali Radix in the Shenqi Fuzheng formula against acute myocardial infarction remains unclear.
May inform preclinical development of traditional formulas for AMI; leaves open clinical translation pending human trials.
The Shenqi Fuzheng (SQ) formula, made from Codonopsis Radix (Dangshen, DS) and Astragali Radix (Huangqi, HQ), has been used in Traditional Chinese Medicine (TCM) and exhibits cardio-protective effects against acute myocardial infarction (AMI). However, the molecular basis of DS-HQ synergy remains unclear. Here, we combined RNA sequencing (RNA-seq) and single-cell RNA sequencing (scRNA-seq) to explore their synergistic mechanisms. Transcriptomic analyses showed that SQ influenced the AMI network more effectively than either herb alone. ScRNA-seq analysis revealed that these synergistic effects involve both direct and indirect pro-angiogenic pathways. The combination treatment enhanced pro-angiogenic responses in microvascular endothelial subpopulations and promoted angiogenesis in the border zone. It also enhanced the anti-inflammatory role of a specific reparative macrophage subset and stimulated vascular endothelial growth factor A (VEGFA) secretion from these cells, supporting the VEGFA-VEGFR signaling between macrophages and microvascular endothelial cells. This coordinated regulation provides a plausible mechanistic explanation for the reduced infarct size and improved cardiac outcomes seen in vivo, highlighting the therapeutic value of TCM.
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Wang et al. (2026) studied Acute myocardial infarction (AMI). Shenqi Fuzheng (SQ) formula vs. Either herb alone (Codonopsis Radix or Astragali Radix) was evaluated on Transcriptomic changes and synergistic mechanisms. Shenqi Fuzheng formula influenced the AMI network more effectively than either herb alone, enhancing pro-angiogenic responses and anti-inflammatory macrophage activity to reduce infarct size in vivo.
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