Abstract: Astragaloside IV (AS-IV), one of the major active constituents of Astragalus membranaceus in Traditional Chinese Medicine, has been widely used to treat ischemic diseases. However, the potential mechanism is this action is unclear. In this study, we tested the hypothesis that AS-IV might promote angiogenesis through multiple signaling pathways. Our data indicate that AS-IV treatment promotes umbilical vein endothelial cells (HUVEC) proliferation, migration, and tube formation. AS-IV treatment also activates JAK2/STAT3 and ERK1/2 signaling pathways, and up-regulates endothelial nitric oxide synthase (eNOS) expression and nitric oxide (NO) production. AS-IV-induced angiogenesis in HUVECs is significantly blocked by specific kinase inhibitors. Our study indicated that AS-IV is a key regulator of NO and angiogenesis through the JAK2/STAT3 and ERK1/2 pathways, which provides a mechanistic basis for the potential use of this compound in the treatment of clinical ischemic diseases.
Keywords: astragaloside IV; angiogenesis; nitric oxide; JAK2/STAT3; ERK1/2
Export to BibTeX
MDPI and ACS Style
Wang, S.-G.; Xu, Y.; Chen, J.-D.; Yang, C.-H.; Chen, X.-H. Astragaloside IV Stimulates Angiogenesis and Increases Nitric Oxide Accumulation via JAK2/STAT3 and ERK1/2 Pathway. Molecules 2013, 18, 12809-12819.
Wang S-G, Xu Y, Chen J-D, Yang C-H, Chen X-H. Astragaloside IV Stimulates Angiogenesis and Increases Nitric Oxide Accumulation via JAK2/STAT3 and ERK1/2 Pathway. Molecules. 2013; 18(10):12809-12819.
Wang, Shi-Guang; Xu, Yan; Chen, Jian-Dong; Yang, Chuan-Hua; Chen, Xiao-Hu. 2013. "Astragaloside IV Stimulates Angiogenesis and Increases Nitric Oxide Accumulation via JAK2/STAT3 and ERK1/2 Pathway." Molecules 18, no. 10: 12809-12819.