Computed tomography of amyloid plaques in a mouse model of Alzheimer's disease using diffraction enhanced imaging

被引:46
|
作者
Connor, Dean M. [1 ]
Benveniste, Helene [2 ,3 ]
Dilmanian, F. Avraham [2 ,4 ]
Kritzer, Mary F. [5 ]
Miller, Lisa M. [1 ]
Zhong, Zhong [1 ]
机构
[1] Brookhaven Natl Lab, Natl Synchrotron Light Source, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Dept Med, Upton, NY 11973 USA
[3] SUNY Stony Brook, Dept Anesthesiol, Stony Brook, NY 11794 USA
[4] SUNY Stony Brook, Dept Radiat Oncol, Stony Brook, NY 11794 USA
[5] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
关键词
MAGNETIC-RESONANCE MICROSCOPY; IN-VIVO; TRANSGENIC MICE; BRAIN; FUTURE; AD;
D O I
10.1016/j.neuroimage.2009.03.019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Our understanding of early development in Alzheimer's disease (AD) is clouded by the scale at which the disease progresses: amyloid beta (A beta) plaques, a hallmark feature of AD, are small (similar to 50 mu m) and low contrast in diagnostic clinical imaging techniques. Diffraction enhanced imaging (DEI), a phase contrast x-ray imaging technique, has greater soft tissue contrast than conventional radiography and generates higher resolution images than magnetic resonance microimaging. Thus, in this proof of principle study, DEI in micro-CT mode was performed on the brains of AD-model mice to determine if DEI can visualize A beta plaques. Results revealed small nodules in the cortex and hippocampus of the brain. Histology confirmed that the features seen in the DEI images of the brain were A beta plaques. Several anatomical structures, including hippocampal subregions and white matter tracks, were also observed. Thus, DEI has strong promise in early diagnosis of AD, as well as general studies of the mouse brain. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:908 / 914
页数:7
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