首页> 外文期刊>Brain research >Reynosin protects against neuronal toxicity in dopamine-induced SH-SY5Y cells and 6-hydroxydopamine-lesioned rats as models of Parkinson's disease: Reciprocal up-regulation of E6-AP and down-regulation of α-synuclein
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Reynosin protects against neuronal toxicity in dopamine-induced SH-SY5Y cells and 6-hydroxydopamine-lesioned rats as models of Parkinson's disease: Reciprocal up-regulation of E6-AP and down-regulation of α-synuclein

机译:作为帕金森病的模型,雷诺菌素可保护多巴胺诱导的SH-SY5Y细胞和6-羟基多巴胺损伤的大鼠免受神经元毒性:E6-AP的相互上调和α-突触核蛋白的下调

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Aggregation of α-synuclein (ASYN) is considered a major determinant of neuronal loss in Parkinson's disease (PD). E6-associated protein (E6-AP), an E3 ubiquitin protein ligase, has been known to promote the degradation of α-synuclein. The aim of this study was to assess the effects of the sesquiterpene lactone reynosin on dopamine (DA)-induced neuronal toxicity and regulation of E6-associated protein and α-synuclein proteins in both in vitro and in vivo models of Parkinson's disease. Usi"ng flow cytometry and western blot analysis, we determined that reynosin significantly protected both against cell death from dopamine-induced toxicity in human neuroblastoma SH-SY5Y cells and against the loss of tyrosine hydroxylase (TH)-positive cells in 6-hydroxydopamine (6-OHDA)-lesioned rats (a rodent Parkinson's disease model system). In addition, reynosin made up-regulation of E6-associated protein expression and down-regulation of the over-expression of α-synuclein protein in both dopamine-treated SH-SY5Y cells and 6-hydroxydopamine-lesioned rats. These results suggest that the protective effect of reynosin against dopamine-induced neuronal cell death may be due to the reciprocal up-regulation of E6-associated protein and down-regulation of α-synuclein protein expression.
机译:α-突触核蛋白(ASYN)的聚集被认为是帕金森氏病(PD)中神经元丢失的主要决定因素。已知E6相关蛋白(E6-AP)是E3泛素蛋白连接酶,可促进α-突触核蛋白的降解。这项研究的目的是评估帕金森氏病的体外和体内模型中倍半萜烯内酯雷诺菌素对多巴胺(DA)诱导的神经元毒性以及E6相关蛋白和α-突触核蛋白蛋白的调节的影响。使用流式细胞仪和蛋白质印迹分析,我们确定了雷诺球蛋白可有效保护细胞免受多巴胺诱导的人神经母细胞瘤SH-SY5Y细胞中多巴胺诱导的毒性的细胞死亡,并防止6-羟基多巴胺(-)中酪氨酸羟化酶(TH)阳性细胞的丢失(6-OHDA)损伤的大鼠(啮齿类动物帕金森氏病模型系统)此外,在多巴胺治疗的SH中,雷诺菌素均上调E6相关蛋白的表达,并下调α-突触核蛋白的过表达。 -SY5Y细胞和6-羟基多巴胺损伤的大鼠,这些结果表明,雷诺菌素对多巴胺诱导的神经元细胞死亡的保护作用可能是由于E6相关蛋白的相互上调和α-突触核蛋白的下调表达。

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