体内
转基因小鼠
淀粉样蛋白(真菌学)
病理
发病机制
荧光
阿尔茨海默病
转基因
临床前影像学
化学
荧光寿命成像显微镜
生物物理学
医学
生物化学
生物
疾病
光学
基因
物理
生物技术
作者
Martin Hintersteiner,Albert Enz,Pascal Frey,Anne-Lise Jaton,Willy Kinzy,Rainer Kneuer,Ulf Neumann,Markus Rudin,Matthias Staufenbiel,Markus Stoeckli,Karl‐Heinz Wiederhold,Hans‐Ulrich Gremlich
摘要
As Alzheimer's disease pathogenesis is associated with the formation of insoluble aggregates of amyloid beta-peptide, approaches allowing the direct, noninvasive visualization of plaque growth in vivo would be beneficial for biomedical research. Here we describe the synthesis and characterization of the near-infrared fluorescence oxazine dye AOI987, which readily penetrates the intact blood-brain barrier and binds to amyloid plaques. Using near-infrared fluorescence imaging, we demonstrated specific interaction of AOI987 with amyloid plaques in APP23 transgenic mice in vivo, as confirmed by postmortem analysis of brain slices. Quantitative analysis revealed increasing fluorescence signal intensity with increasing plaque load of the animals, and significant binding of AOI987 was observed for APP23 transgenic mice aged 9 months and older. Thus, AOI987 is an attractive probe to noninvasively monitor disease progression in animal models of Alzheimer disease and to evaluate effects of potential Alzheimer disease drugs on the plaque load.
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