Suppr超能文献

口服三苯甲烷类食用染料类似物亮蓝G可预防APPSwDI/NOS2-/-小鼠模型中的神经元丢失。

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

作者信息

Irwin Jacob A, Erisir Alev, Kwon Inchan

机构信息

102 Gilmer Hall, PO Box 400400, Department of Psychology, University of Virginia, Charlottesville, Virginia 22904, USA.

School of Materials Science and Engineering, Gwangju Institute of Science and Technology, 123 Cheomdan-gwagiro, Buk-gu, Gwangju 61005, Republic of Korea.

出版信息

Curr Alzheimer Res. 2016;13(6):663-77. doi: 10.2174/15672050136661602081424568.

Abstract

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.

摘要

减少淀粉样蛋白-β(Aβ)的积累是开发阿尔茨海默病(AD)治疗方法的一种有前景的策略。我们最近报道,一种三苯甲烷食用染料类似物,亮蓝G(BBG),在基于细胞的实验中是体外淀粉样蛋白-β聚集和细胞毒性的剂量依赖性调节剂。在这项最新工作的基础上,我们试图在与治疗相关的AD转基因小鼠模型中进一步评估这种新型调节剂。将BBG口服给予APPSwDI/NOS2-/-小鼠三个月,以评估其生物相容性、穿过血脑屏障的通透性以及挽救AD病理的功效。结果表明,BBG耐受性良好,未引起显著体重变化/异常行为,并且能够在APPSwDI/NOS2-/-小鼠中显著穿过AD血脑屏障。对脑切片的免疫组织化学和电子显微镜分析表明,BBG能够显著预防神经元丢失并减少海马神经元中的细胞内APP/Aβ。这是关于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影响蛋白质构象/聚集疾病以及3)对APPSwDI/NOS2-/-小鼠AD病理进行电子显微镜超微结构分析的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f062/5441128/2556b0f56a07/CAR-13-663_F1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验