Petiet Alexandra, Delatour Benoit, Dhenain Marc
CNRS, URA 2210, Fontenay aux Roses, France.
Methods Mol Biol. 2011;771:293-308. doi: 10.1007/978-1-61779-219-9_16.
Alzheimer's disease (AD) is an important social and economic issue for our societies. The development of therapeutics against this severe dementia requires assessing the effects of new drugs in animal models thanks to dedicated biomarkers. According to the amyloid cascade hypothesis, β-amyloid deposits are at the origin of most of the lesions associated with AD. These extracellular deposits are therefore one of the main targets in therapeutical strategies. Aβ peptides can be revealed histologically with specific dyes or antibodies, or by magnetic resonance microscopy (μMRI) that uses their association with iron as a source of signal. The microscopic size of the lesions necessitates the development of specific imaging protocols. Most protocols use T (2)-weighted sequences that reveal the aggregates as hypointense spots. This chapter describes histological methods that reveal amyloid plaques with specific stains and MR-imaging protocols for in vivo and ex vivo MR imaging of AD mice.
阿尔茨海默病(AD)对我们的社会而言是一个重要的社会和经济问题。对抗这种严重痴呆症的治疗方法的开发需要借助专门的生物标志物来评估新药在动物模型中的效果。根据淀粉样蛋白级联假说,β-淀粉样蛋白沉积是大多数与AD相关病变的根源。因此,这些细胞外沉积物是治疗策略的主要靶点之一。Aβ肽可以通过特定染料或抗体进行组织学显示,也可以通过磁共振显微镜(μMRI)来显示,μMRI利用其与铁的结合作为信号源。病变的微观尺寸使得开发特定的成像方案成为必要。大多数方案使用T(2)加权序列,将聚集体显示为低信号点。本章描述了用特定染色剂显示淀粉样斑块的组织学方法以及用于AD小鼠体内和体外磁共振成像的磁共振成像方案。