Astragaloside IV Stimulates Angiogenesis and Increases Nitric Oxide Accumulation via JAK2/STAT3 and ERK1/2 Pathway

被引:87
作者
Wang, Shi-Guang [1 ,2 ]
Xu, Yan [3 ]
Chen, Jian-Dong [2 ]
Yang, Chuan-Hua [4 ]
Chen, Xiao-Hu [2 ]
机构
[1] Nanjing Univ Chinese Med, Clin Med Coll 1, Nanjing 210023, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Dept Cardiol, Jiangsu Prov Hosp Tradit Chinese Med, Affiliated Hosp, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Coll Basic Med Sci, Nanjing 210023, Jiangsu, Peoples R China
[4] Shandong Univ Tradit Chinese Med, Dept Cardiol, Affiliated Hosp, Jinan 250011, Peoples R China
关键词
astragaloside IV; angiogenesis; nitric oxide; JAK2/STAT3; ERK1/2; ENDOTHELIAL GROWTH-FACTOR; IN-VITRO; THERAPEUTIC ANGIOGENESIS; ISCHEMIA; SYNTHASE; CELLS; INJURY; VIVO; INHIBITION; EXPRESSION;
D O I
10.3390/molecules181012809
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:12809 / 12819
页数:11
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