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Pterostilbene impact on retinal endothelial cells under high glucose environment

机译:在高糖环境下紫檀萜对视网膜内皮细胞的影响

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摘要

Diabetic retinopathy (DR) has complicated pathogenic factors. Studies showed that DR belongs to chronic inflammatory disease, and retinal endothelial cells oxidation by free radicals is one of its mechanisms. Pterostilbene, as the homologous derivative of resveratrol, has obvious antioxidant effect. Its influence on the DR has not been studied. This study intended to investigate the effect and mechanism of pterostilbene on human retinal endothelial cells (hRECs) under high glucose environment to illustrate pterostilbene impact on DR and provide basis for DR clinical treatment. hRECs cultured in high glucose environment were treated by 1.0 mmol/L pterostilbene. MTT assay was applied to test cell proliferation. ELISA was used to detect inflammatory factor TNF-α and IL-1β content. Real time PCR and Western blot were performed to examine NF-κB mRNA and protein expression. ROS and SOD activities were analyzed. Under high glucose environment, hRECs proliferation increased, TNF-α and IL-1β expression elevated, and NF-κB protein level upregulated significantly. On the other side, ROS production increased and SOD activity decreased obviously (P < 0.05). Pterostilbene can suppress hRECs over proliferation, decrease TNF-α and IL-1β, inhibit NF-κB protein expression, reduce ROS production, and increase SOD activity markedly compared with high glucose group (P < 0.05). Pterostilbene may delay DR progress through alleviating inflammation and antioxidation to suppress hRECs over proliferation.
机译:糖尿病性视网膜病(DR)具有复杂的致病因素。研究表明,DR属于慢性炎症性疾病,视网膜内皮细胞被自由基氧化是其机制之一。萜烯作为白藜芦醇的同源衍生物,具有明显的抗氧化作用。尚未研究其对DR的影响。这项研究旨在探讨在高葡萄糖环境下蝶草皮对人视网膜内皮细胞(hRECs)的作用和机制,以阐明蝶草皮对DR的影响,并为DR临床治疗提供依据。在高葡萄糖环境中培养的hRECs用1.0 mmol / L萜烯二苯处理。将MTT测定法用于测试细胞增殖。 ELISA用于检测炎性因子TNF-α和IL-1β的含量。进行实时PCR和Western印迹以检查NF-κBmRNA和蛋白表达。分析了ROS和SOD活性。在高糖环境下,hRECs增殖增加,TNF-α和IL-1β表达升高,NF-κB蛋白水平明显升高。另一方面,ROS产量增加,SOD活性明显下降(P <0.05)。与高糖组相比,蝶呤能抑制hRECs过度增殖,降低TNF-α和IL-1β,抑制NF-κB蛋白表达,减少ROS的产生,并增加SOD活性(P <0.05)。蝶烯可以通过减轻炎症和抗氧化作用来抑制DR的进展,从而抑制hRECs过度增殖。

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