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Integrative multi-Omics and network pharmacology reveal angiogenesis promotion by Quan-Du-Zhong Capsule via VEGFA/PI3K-Akt pathway. | LitMetric

Integrative multi-Omics and network pharmacology reveal angiogenesis promotion by Quan-Du-Zhong Capsule via VEGFA/PI3K-Akt pathway.

J Ethnopharmacol

Shanghai Frontiers Science Center of TCM Chemical Biology, Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China. Electronic address:

Published: December 2024

AI Article Synopsis

  • Quan-du-zhong capsule (QDZ) is a traditional Chinese herbal remedy derived from Eucommia ulmoides, primarily used for vascular diseases like hypertension and osteoporosis, but its effect on promoting blood vessel formation (pro-angiogenic effect) needs more research.* -
  • The study investigated QDZ's pro-angiogenic properties through various lab assays and in vivo models, revealing that it significantly enhances the growth and migration of human endothelial cells and promotes blood flow recovery in mice after ischemic events.* -
  • Analysis identified 49 compounds in QDZ, and the mechanisms behind its effects were linked to the VEGFA/PI3K-Akt signaling pathway, highlighting the role of specific proteins involved in angiogenesis

Article Abstract

Ethnopharmacological Relevance: Quan-du-zhong capsule (QDZ), derived from the whole plant extract of Eucommiaulmoides Oliv., is a traditional Chinese herbal medicine used in treating vascular-related diseases, including hypertension and osteoporosis. Despite its established uses, its pro-angiogenic effects and underlying mechanisms require further investigation.

Aim Of This Study: This study aims to investigate the pro-angiogenic effects of QDZ and explore the underlying mechanisms.

Materials And Methods: The chemical compositions of QDZ, including its absorbed prototypes in rats, were analyzed using UHPLC-Q Exactive-Orbitrap-MS. The pro-angiogenic activities of QDZ were evaluated in human umbilical vein endothelial cells (HUVECs) through various assays, including CCK-8, migration, scratch, tubule formation, and 3D sprouting assays. Additionally, the pro-angiogenic effects of QDZ were further assessed invivo through the matrigel plug assay and a hindlimb ischemia-reperfusion model, with three-dimensional blood flow visualized via micro-CT. A comprehensive approach involving network pharmacology, molecular docking, transcriptomics, and proteomics was utilized to explore the pro-angiogenic mechanism of QDZ, with validation by Western blot analysis.

Results: QDZ significantly promoted the proliferation, migration, and tubule formation of HUVECs. The matrigel plug assay further confirmed its pro-angiogenic potential. Invivo, QDZ-treated mice displayed enhanced vascular distribution and faster blood flow recovery post-ischemia-reperfusion. Chemical analysis identified 49 compounds in QDZ, with 16 absorbed prototypes detected in rat plasma. Mechanistic investigations through network pharmacology, transcriptomics, and proteomics suggested that QDZ's pro-angiogenic effects were mediated through the VEGFA/PI3K-Akt signaling pathway, with increased phosphorylation of angiogenesis-related proteins such as PI3K, Akt, FAK, and Src.

Conclusions: This study demonstrates that QDZ promotes angiogenesis via activating the VEGFA and its downstream PI3K-Akt signaling pathway, shedding light on the mechanisms that underpin its traditional medicinal use in vascular health.

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Source
http://dx.doi.org/10.1016/j.jep.2024.119222DOI Listing

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