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Inhibition of Hypoxia-Induced Retinal Angiogenesis by Specnuezhenide, an Effective Constituent of Ligustrum lucidum Ait., through Suppression of the HIF-1 alpha/VEGF Signaling Pathway

机译:Specnuezhenide通过抑制HIF-1 alpha / VEGF信号通路抑制女贞子的有效成分,从而抑制缺氧诱导的视网膜血管生成。

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Specnuezhenide (SPN), one of the main ingredients of Chinese medicine "Nu-zhen-zi", has anti-angiogenic and vision improvement effects. However, studies of its effect on retinal neovascularization are limited so far. In the present study, we established a vascular endothelial growth factor A (VEGFA) secretion model of human acute retinal pigment epithelial-19 (ARPE-19) cells by exposure of 150 mu M CoCl2 to the cells and determined the VEGFA concentrations, the mRNA expressions of VEGFA, hypoxia inducible factor-1 alpha (HIF-1 alpha) & prolyl hydroxylases 2 (PHD-2), and the protein expressions of HIF-1 alpha and PHD-2 after treatment of 3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole (YC-1, 1.0 mu g/mL) or SPN (0.2, 1.0 and 5.0 mu g/mL). Furthermore, rat pups with retinopathy were treated with SPN (5.0 and 10.0 mg/kg) in an 80% oxygen atmosphere and the retinal avascular areas were assessed through visualization using infusion of ADPase and H&E stains. The results showed that SPN inhibited VEGFA secretion by ARPE-19 cells under hypoxia condition, down-regulated the mRNA expressions of VEGFA and PHD-2 slightly, and the protein expressions of VEGFA, HIF-1 alpha and PHD-2 significantly in vitro. SPN also prevented hypoxia-induced retinal neovascularization in a rat model of oxygen-induced retinopathy in vivo. These results indicate that SPN ameliorates retinal neovascularization through inhibition of HIF-1 alpha/VEGF signaling pathway. Therefore, SPN has the potential to be developed as an agent for the prevention and treatment of diabetic retinopathy.
机译:Specnuezhenide(SPN)是中药“女贞子”的主要成分之一,具有抗血管生成和改善视力的作用。然而,迄今为止,其对视网膜新血管形成的作用的研究还很有限。在本研究中,我们通过将150μM CoCl2暴露于人急性视网膜色素上皮19(ARPE-19)细胞,建立了人血管内皮生长因子A(VEGFA)分泌模型,并测定了VEGFA浓度,mRNA 3-(5'-羟甲基-)处理后,VEGFA,缺氧诱导因子-1α(HIF-1 alpha)和脯氨酰羟化酶2(PHD-2)的表达以及HIF-1 alpha和PHD-2的蛋白表达2'-呋喃基)-1-苄基吲唑(YC-1,1.0μg / mL)或SPN(0.2,1.0和5.0μg/ mL)。此外,在80%的氧气气氛中用SPN(5.0和10.0 mg / kg)处理患有视网膜病变的幼崽,并通过注入ADPase和H&E染色剂通过可视化评估视网膜无血管区域。结果表明,SPN在缺氧条件下能抑制ARPE-19细胞分泌VEGFA,并下调VEGFA和PHD-2的mRNA表达,并显着抑制VEGFA,HIF-1α和PHD-2的蛋白表达。 SPN还可以在体内氧诱导的视网膜病变大鼠模型中预防缺氧诱导的视网膜新血管形成。这些结果表明,SPN通过抑制HIF-1α/ VEGF信号通路改善了视网膜新血管形成。因此,SPN有潜力被开发为预防和治疗糖尿病性视网膜病的药物。

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