Title of article :
A non-toxic ligand for voxel-based MRI analysis of plaques in AD transgenic mice
Author/Authors :
Einar M. Sigurdsson، نويسنده , , Youssef Z. Wadghiri، نويسنده , , Lisa Mosconi، نويسنده , , Jeffrey A. Blind، نويسنده , , Elin Knudsen، نويسنده , , Ayodeji Asuni، نويسنده , , Henrieta Scholtzova، نويسنده , , Wai H. Tsui، نويسنده , , Yongsheng Li، نويسنده , , Martin Sadowski، نويسنده , , Daniel H. Turnbull، نويسنده , , Mony J. de Leon، نويسنده , , Thomas Wisniewski، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
12
From page :
836
To page :
847
Abstract :
Amyloid plaques are a characteristic feature in Alzheimerʹs disease (AD). A novel non-toxic contrast agent is presented, Gd-DTPA-K6Aβ1–30, which is homologous to Aβ, and allows plaque detection in vivo. μMRI was performed on AD model mice and controls prior to and following intracarotid injection with Gd-DTPA-K6Aβ1–30 in mannitol solution, to transiently open the blood–brain barrier. A gradient echo T2*-weighted sequence was used to provide 100 μm 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-K6Aβ1–30 is an effective, non-toxic, ligand for plaque detection when combined with VBA (p ≤ 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.
Keywords :
Iron , transgenic mice , Voxel-based analysis , imaging , magnetic resonance imaging , amyloid , Alzheimer’s Disease
Journal title :
Neurobiology of Aging
Serial Year :
2008
Journal title :
Neurobiology of Aging
Record number :
821188
Link To Document :
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