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Tetrahydroxystilbene glucoside antagonizes age-related α-synuclein overexpression in the hippocampus of APP transgenic mouse model of Alzheimer's disease

机译:四羟基二苯乙烯苷可拮抗老年痴呆症APP转基因小鼠模型海马中与年龄相关的α-突触核蛋白过表达

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Purpose: To investigate the mRNA and protein alterations of α-synuclein in the brain of Alzheimer's disease-like mouse model at the different ages, and to evaluate the effects of 2,3,5,4′-tetrahydroxy stilbene-2-O-β-D-glucoside (TSG) on α-synuclein expression. Methods: TSG (120 or 240 μmol kg-1d-1) was intragastrically administered to APPV717I transgenic (Tg) mice at 4- or 10-month-old for 6 months. Results: mRNA expression of α-synuclein increased in hippocampus in 4 month to 16 month old Tg mice compared with age-matched control. α-synuclein protein expression in hippocampus also increased in 4 month to 16 month old Tg mice significantly. Significant down-regulation of α-synuclein mRNA and protein expression in hippocampus was found after treatment of TSG for 6 months in both 10- and 16-month-old Tg mice. Production of dimer and tetramer of α-synuclein protein in Tg mice was inhibited after treatment with TSG. Conclusions: The expression and aggregation of α-synuclein was age-dependently increased in Tg mice. TSG not only prevents over-expression of α-synuclein at an early stage, but also reverses the increased expression of α-synuclein and inhibits the aggregation at the late stage of Tg mice. TSG may have potential to the prevention and treatment of Alzheimer's diseases.
机译:目的:研究不同年龄的阿尔茨海默病样小鼠模型脑中α-突触核蛋白的mRNA和蛋白变化,并评价2,3,5,4'-四羟基-2-O-的作用β-D-葡萄糖苷(TSG)对α-突触核蛋白的表达。方法:将4或10个月大的APPV717I转基因(Tg)小鼠胃内给予TSG(120或240μmolkg-1d-1),持续6个月。结果:与年龄匹配的对照组相比,在4个月至16个月大的Tg小鼠中海马中α-突触核蛋白的mRNA表达增加。在4个月至16个月大的Tg小鼠中,海马中的α-突触核蛋白蛋白表达也显着增加。在10个月和16个月大的Tg小鼠中,TSG治疗6个月后,发现海马中α-突触核蛋白mRNA和蛋白表达显着下调。用TSG处理后,可抑制Tg小鼠中α-突触核蛋白蛋白的二聚体和四聚体的产生。结论:Tg小鼠中α-突触核蛋白的表达和聚集随年龄的增长而增加。 TSG不仅可以在早期阻止α-突触核蛋白的过表达,而且可以逆转α-突触核蛋白的表达增加并在Tg小鼠的晚期抑制聚集。 TSG可能具有预防和治疗阿尔茨海默氏病的潜力。

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