Sigurdsson Einar M, Wadghiri Youssef Z, Mosconi Lisa, Blind Jeffrey A, Knudsen Elin, Asuni Ayodeji, Scholtzova Henrieta, Tsui Wai H, Li Yongsheng, Sadowski Martin, Turnbull Daniel H, de Leon Mony J, Wisniewski Thomas
Department of Psychiatry, New York University School of Medicine, New York, NY 10016, USA.
Neurobiol Aging. 2008 Jun;29(6):836-47. doi: 10.1016/j.neurobiolaging.2006.12.018. Epub 2007 Feb 8.
Amyloid plaques are a characteristic feature in Alzheimer's disease (AD). A novel non-toxic contrast agent is presented, Gd-DTPA-K6Abeta1-30, which is homologous to Abeta, and allows plaque detection in vivo. microMRI was performed on AD model mice and controls prior to and following intracarotid injection with Gd-DTPA-K6Abeta1-30 in mannitol solution, to transiently open the blood-brain barrier. A gradient echo T2(*)-weighted sequence was used to provide 100 microm isotropic resolution with imaging times of 115 min. The scans were examined with voxel-based analysis (VBA) using statistical parametric mapping, for un-biased quantitative comparison of ligand-injected mice and controls. The results indicate that: (1) Gd-DTPA-K6Abeta1-30 is an effective, non-toxic, ligand for plaque detection when combined with VBA (p< or =0.01-0.001), comparing pre and post-ligand injection scans. (2) Large plaques can be detected without the use of a contrast agent and this detection co-localizes with iron deposition. (3) Smaller, earlier plaques require contrast ligand for MRI visualization. Our ligand when combined with VBA may be useful for following therapeutic approaches targeting amyloid in transgenic mouse models.
淀粉样斑块是阿尔茨海默病(AD)的一个特征性表现。本文介绍了一种新型无毒造影剂Gd-DTPA-K6Abeta1-30,它与β淀粉样蛋白(Aβ)同源,能够在体内检测斑块。在用甘露醇溶液配制的Gd-DTPA-K6Abeta1-30经颈动脉注射给AD模型小鼠和对照小鼠前后,进行了显微磁共振成像(microMRI),以短暂打开血脑屏障。使用梯度回波T2(*)加权序列,以提供100微米各向同性分辨率,成像时间为115分钟。使用统计参数映射的基于体素的分析(VBA)对扫描结果进行检查,以对注射配体的小鼠和对照进行无偏定量比较。结果表明:(1)与VBA结合时,Gd-DTPA-K6Abeta1-30是一种用于检测斑块的有效、无毒配体(p≤0.01-0.001),比较配体注射前后的扫描结果。(2)无需使用造影剂即可检测到大斑块,且这种检测与铁沉积共定位。(3)较小的早期斑块需要造影配体用于MRI可视化。我们的配体与VBA结合可能有助于在转基因小鼠模型中跟踪针对淀粉样蛋白的治疗方法。