Lv Kongpeng, Ren Qin, Zhang Xingyan, Zhang Keda, Fei Jia, Li Tiyuan
Shenzhen Infectious Disease Medicine Engineering Center, Shenzhen People's Hospital, 2nd Clinical Medical College of Jinan University Shenzhen 518120 Guangdong Province China
Integrated Chinese and Western Medicine Postdoctoral Research Station, Jinan University Guangzhou 510632 Guangdong Province China
RSC Adv. 2019 Jul 25;9(40):22921-22930. doi: 10.1039/c9ra01673b. eCollection 2019 Jul 23.
Astilbin is a dihydroflavonol natural product isolated from a variety of food and medicinal herbs ( Roxb.), and its mechanism of action in vascular pharmacology remains unclear. The aim of this study was to investigate the pro-angiogenic effects of astilbin and its putative mechanism of action. Briefly, our studies showed a dose-dependent ability of astilbin to increase the ability of HUVECs to proliferate and migrate, and undergo cell invasion and tube formation. Moreover, astilbin significantly increased the expression levels of several major proteins involved in the angiogenesis pathway, PI3K, Akt, p38 and ERK1/2. Our studies demonstrated the ability of astilbin to significantly restore the blood vessel loss induced by VRI in a VRI-induced vascular insufficiency zebrafish model. In conclusion, in this study we first demonstrate that astilbin exhibits pro-angiogenic activity in HUVECs and VRI-induced vascular insufficient zebrafish, possibly through the activation of the PI3K/Akt and MAPK/ERK dependent signaling pathways. These findings suggest that astilbin could be further developed as a potential agent in the prevention or treatment of insufficient angiogenesis related diseases in the future.
落新妇苷是一种从多种食用和药用草本植物(虎杖)中分离出的二氢黄酮醇天然产物,其在血管药理学中的作用机制尚不清楚。本研究的目的是研究落新妇苷的促血管生成作用及其可能的作用机制。简而言之,我们的研究表明落新妇苷具有剂量依赖性,可增强人脐静脉内皮细胞(HUVECs)的增殖、迁移能力,并促进细胞侵袭和管腔形成。此外,落新妇苷显著提高了血管生成途径中几种主要蛋白质PI3K、Akt、p38和ERK1/2的表达水平。我们的研究证明,在血管生成相关视网膜病变(VRI)诱导的血管功能不全斑马鱼模型中,落新妇苷能够显著恢复由VRI引起的血管损失。总之,在本研究中,我们首次证明落新妇苷在HUVECs和VRI诱导的血管功能不全斑马鱼中表现出促血管生成活性,可能是通过激活PI3K/Akt和MAPK/ERK依赖性信号通路。这些发现表明,落新妇苷未来可能作为一种潜在药物,用于预防或治疗与血管生成不足相关的疾病。