Key result
Ginsenoside extracts from Panax quinquefolius promoted intersegmental vessel growth in a zebrafish model and targeted VEGF, FGF2, and STAT3 pathways in network pharmacology analysis.
Ginsenosides from Panax quinquefolius promote angiogenesis in a zebrafish model and may target VEGF, FGF2, and STAT3 pathways, suggesting potential nutraceutical benefits for cardiovascular disease.
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Precludes clinical recommendations; leaves open hypothesis-generating potential for ginsenoside nutraceuticals in angiogenesis-related cardiovascular disease.
Seven main ginsenosides, including ginsenoside Re, ginsenoside Rb1, pseudoginsenoside F11, ginsenoside Rb2, ginsenoside Rb3, ginsenoside Rd, and ginsenoside F2, were identified by LC-QTOF MS/MS from root, leaf and flower extracts of Panax quinquefolius. These extracts promoted intersegmental vessel growth in a zebrafish model, indicating their potential cardiovascular health benefits. Network pharmacology analysis was then conducted to reveal the potential mechanisms of ginsenoside activity in the treatment of coronary artery disease. GO and KEGG enrichment analyses elucidated that G protein-coupled receptors played a critical role in VEGF-mediated signal transduction and that the molecular pathways associated with ginsenoside activity are involved in neuroactive ligand–receptor interaction, cholesterol metabolism, the cGMP–PKG signaling pathway, etc. Moreover, VEGF, FGF2, and STAT3 were confirmed as the major targets inducing proliferation of endothelial cells and driving the pro-angiogenic process. Overall, ginsenosides could be potent nutraceutical agents that act to reduce the risks of cardiovascular disease. Our findings will provide a basis to utilize the whole P. quinquefolius plant in drugs and functional foods.
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Zhang et al. (2023) studied Coronary artery disease. Ginsenosides from Panax quinquefolius extracts was evaluated on Intersegmental vessel growth and network pharmacology targets. Ginsenoside extracts from Panax quinquefolius promoted intersegmental vessel growth in a zebrafish model and targeted VEGF, FGF2, and STAT3 pathways in network pharmacology analysis.
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