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Kaempferol inhibited VEGF and PGF expression and invitro angiogenesis of HRECs under diabetic-likeenvironment

机译:山萘酚可抑制VEGF和PGF的表达以及类糖尿病患者下HRECs的体外血管生成环境

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摘要

Diabetic retinopathy (DR) is one of the common and specific microvascular complications of diabetes. This study aimed to investigate the anti-angiogenic effect of kaempferol and explore its underlying molecular mechanisms. The mRNA expression level of vascular endothelial growth factor (VEGF) and placenta growth factor (PGF) and the concentrations of secreted VEGF and PGF were measured by qTR-PCR and ELISA assay, respectively. Human retinal endothelial cells (HRECs) proliferation, migration, and sprouting were measured by CCK-8 and transwell, scratching wound, and tube formation assays, respectively. Protein levels were determined by western blot. High glucose (25 mM) increased the mRNA expression levels of VEGF and PGF as well as the concentrations of secreted VEGF and PGF in HRECs, which can be antagonized by kaempferol (25 µM). Kaempferol (5-25 µM) significantly suppressed cell proliferation, migration, migration distance and sprouting of HRECs under high glucose condition. The anti-angiogenic effect of kaempferol was mediated via downregulating the expression of PI3K and inhibiting the activation of Erk1/2, Src, and Akt1. This study indicates that kaempferol suppressed angiogenesis of HRECs via targeting VEGF and PGF to inhibit the activation of Src-Akt1-Erk1/2 signaling pathway. The results suggest that kaempferol may be a potential drug for better management of DR.
机译:糖尿病性视网膜病(DR)是糖尿病的常见和特定的微血管并发症之一。这项研究旨在调查山奈酚的抗血管生成作用,并探讨其潜在的分子机制。用qTR-PCR和ELISA法分别检测血管内皮生长因子(VEGF)和胎盘生长因子(PGF)的mRNA表达水平以及分泌的VEGF和PGF的浓度。人视网膜内皮细胞(HRECs)的增殖,迁移和发芽分别通过CCK-8和Transwell,抓挠伤口和管形成试验进行了测定。通过蛋白质印迹法测定蛋白质水平。高葡萄糖(25 mM)可以增加HREC中VEGF和PGF的mRNA表达水平,以及分泌的VEGF和PGF的浓度,而山fer酚(25 µM)可以拮抗该水平。山茱fer醇(5-25 µM)在高葡萄糖条件下显着抑制HRECs的细胞增殖,迁移,迁移距离和发芽。山emp酚的抗血管生成作用是通过下调PI3K的表达并抑制Erk1 / 2,Src和Akt1的激活来介导的。这项研究表明山emp酚通过靶向VEGF和PGF抑制Src-Akt1-Erk1 / 2信号通路的激活来抑制HREC的血管生成。结果表明山emp酚可能是更好地管理DR的潜在药物。

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