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首页> 外文期刊>BMC research notes >Protective effects of flavonol isoquercitrin, against 6-hydroxy dopamine (6-OHDA) - induced toxicity in PC12 cells
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Protective effects of flavonol isoquercitrin, against 6-hydroxy dopamine (6-OHDA) - induced toxicity in PC12 cells

机译:黄酮醇异槲皮苷对6-羟基多巴胺(6-OHDA)诱导的PC12细胞毒性的保护作用

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Background Free radicals-induced neurodegeneration is one of the many causes of Parkinson’s disease (PD). This study investigated the neuroprotective effects of flavonol isoquercitrin against toxicity induced by 6-hydroxy-dopamine (6-OHDA) in rat pheochromocytoma (PC12) cells. Methods PC12 cells were pretreated with different concentrations of isoquercitrin for 4, 8 and 12 hours and incubated with 6-OHDA for 24 hours to induce oxidative cell damage. Results A significant cytoprotective activity was observed in isoquercitrin pre-treated cells in a dose-dependent manner. There was a significant increase (P Conclusions The present study suggests the protective role of isoquercitrin on 6-hydroxydopamine-induced toxicity by virtue of its antioxidant potential. Isoquercitrin could be a potential therapeutic agent against neurodegeneration in Parkinson’s disease.
机译:背景自由基引起的神经变性是帕金森氏病(PD)的多种原因之一。这项研究调查了黄酮醇异槲皮苷对大鼠嗜铬细胞瘤(PC12)细胞中6-羟基多巴胺(6-OHDA)诱导的毒性的神经保护作用。方法用不同浓度的异槲皮苷预处理PC12细胞4、8、12小时,并与6-OHDA孵育24小时,以诱导氧化性细胞损伤。结果在异槲皮苷预处理的细胞中以剂量依赖性方式观察到显着的细胞保护活性。 (P结论这项研究表明,异槲皮苷具有抗氧化作用,对6-羟基多巴胺引起的毒性具有保护作用。异槲皮苷可能是对抗帕金森氏病神经退行性变的潜在治疗剂。

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