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Oral Triphenylmethane Food Dye Analog Brilliant Blue G Prevents Neuronal Loss in APPSwDI/NOS2-/- Mouse Model

机译:口服三苯甲烷食用染料类似物亮蓝G可防止APPSwDI / NOS2-/-小鼠模型中的神经元丢失

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摘要

Reducing amyloid-β (Aβ) accumulation is a promising strategy for developing Alzheimer’s Disease (AD) therapeutics. We recently reported that a triphenylmethane food dye analog, Brilliant Blue G (BBG), is a dose-dependent modulator of in vitro amyloid-β aggregation and cytotoxicity in cell-based assays. Following up on this recent work, we sought to further evaluate this novel modulator in a therapeutically-relevant AD transgenic mouse model. BBG was orally administered to APPSwDI/NOS2-/- mice for three months in order to assess its biocompatibility, its permeability across the blood-brain barrier, and its efficacy at rescuing AD pathology. The results showed that BBG was well-tolerated, caused no significant weight change/unusual behavior, and was able to significantly cross the AD blood-brain barrier in APPSwDI/NOS2-/- mice. Immunohistochemical and electron microscopic analysis of the brain sections revealed that BBG was able to significantly prevent neuronal loss and reduce intracellular APP/Aβ in hippocampal neurons. This is the first report of 1) the effect of Brilliant Blue G on neuronal loss in a transgenic animal model of AD, 2) oral administration of BBG to affect a protein conformation/aggregation disease, and 3) electron microscopic ultrastructural analysis of AD pathology in APPSwDI/NOS2-/- mice.
机译:减少淀粉样β(Aβ)积累是开发阿尔茨海默氏病(AD)治疗剂的一种有前途的策略。我们最近报道了三苯基甲烷食用染料类似物,亮蓝G(BBG),是基于细胞的测定中体外淀粉样β聚集和细胞毒性的剂量依赖性调节剂。跟踪这项最新工作,我们试图在治疗相关的AD转基因小鼠模型中进一步评估这种新型调节剂。为了评估其生物相容性,穿过血脑屏障的通透性及其在挽救AD病理学方面的功效,BBG口服给予APPSwDI / NOS2-/-小鼠三个月。结果表明,BBG具有良好的耐受性,不会引起明显的体重变化/异常行为,并且能够显着越过APPSwDI / NOS2-/-小鼠的AD血脑屏障。脑切片的免疫组织化学和电子显微镜分析表明,BBG能够显着预防神经元丢失并减少海马神经元的细胞内APP /Aβ。这是第一个报告:1)亮蓝G对AD转基因动物模型中神经元丢失的影响; 2)口服BBG以影响蛋白质构象/聚集疾病; 3)AD病理的电子显微超微结构分析在APPSwDI / NOS2-/-小鼠中。

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