Department of Materials Sciences, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tennoudai 1-1-1, Tsukuba, Ibaraki, 305-8573, Japan.
School of Pharmacy, Walailak University, Thasala, Nakhon Si Thammarat, 80161, Thailand.
Sci Rep. 2017 Jun 19;7(1):3785. doi: 10.1038/s41598-017-03411-7.
The present study aimed to assess whether our newly developed redox nanoparticle (RNP) that has antioxidant potential decreases Aβ levels or prevents Aβ aggregation associated with oxidative stress. The transgenic Tg2576 Alzheimer's disease (AD) mice were used to investigate the effect of chronic ad libitum drinking of RNP solution for 6 months, including memory and learning functions, antioxidant activity, and amyloid plaque aggregation. The results showed that RNP-treated mice had significantly attenuated cognitive deficits of both spatial and non-spatial memories, reduced oxidative stress of lipid peroxide, and DNA oxidation. RNP treatment increased the percent inhibition of superoxide anion and glutathione peroxidase activity, neuronal densities in the cortex and hippocampus, decreased Aβ(1-40), Aβ(1-42) and gamma (γ)-secretase levels, and reduced Aβ plaque observed using immunohistochemistry analysis and thioflavin S staining. Our results suggest that RNP may be a promising candidate for AD therapy because of its antioxidant properties and reduction in Aβ aggregation, thereby suppressing its adverse side effect.
本研究旨在评估我们新开发的具有抗氧化潜力的氧化还原纳米颗粒(RNP)是否能降低 Aβ 水平或预防与氧化应激相关的 Aβ 聚集。使用转 AD 基因 Tg2576 小鼠来研究 6 个月自由饮用 RNP 溶液对其的影响,包括记忆和学习功能、抗氧化活性和淀粉样斑块聚集。结果表明,RNP 处理的小鼠的空间和非空间记忆认知缺陷明显减轻,脂质过氧化物、DNA 氧化的氧化应激降低。RNP 治疗增加了超氧阴离子和谷胱甘肽过氧化物酶活性的抑制率,皮质和海马中的神经元密度,降低了 Aβ(1-40)、Aβ(1-42)和γ(γ)-分泌酶水平,并减少了免疫组织化学分析和硫黄素 S 染色观察到的 Aβ 斑块。我们的结果表明,RNP 可能是 AD 治疗的有前途的候选药物,因为它具有抗氧化特性和降低 Aβ 聚集的能力,从而抑制其不良的副作用。