Quantitative intact specimen magnetic resonance microscopy at 3.0 T

被引:6
作者
Bath, Kevin G. [1 ]
Voss, Henning U. [2 ]
Jing, Deqiang [1 ]
Anderson, Stewart [1 ]
Hempstead, Barbara [4 ]
Lee, Francis S. [1 ]
Dyke, Jonathan P. [2 ]
Ballon, Douglas J. [2 ,3 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Psychiat, New York, NY 10065 USA
[2] Cornell Univ, Weill Cornell Med Coll, Dept Radiol, New York, NY 10065 USA
[3] Cornell Univ, Weill Grad Sch Med Sci, Dept Physiol Biophys & Syst Biol, New York, NY 10065 USA
[4] Cornell Univ, Weill Cornell Med Coll, Div Hematol & Med Oncol, Dept Med, New York, NY 10065 USA
关键词
Magnetic resonance microscopy (MRM); Mouse; Neuroanatomy; TrkB; FoxG1; OLFACTORY-BULB; MR MICROSCOPY; MOUSE-BRAIN; CELL-DEATH; IN-VIVO; TRKB; HAPLOINSUFFICIENCY; NEUROTROPHINS; NEUROGENESIS; HIPPOCAMPUS;
D O I
10.1016/j.mri.2008.11.008
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
In this report, we discuss the application of a methodology for high-contrast, high-resolution magnetic resonance microscopy (MRM) of murine tissue using a 3.0-T imaging system. We employed a threefold strategy that included customized specimen preparation to maximize image contrast, three-dimensional data acquisition to minimize scan time and custom radiofrequency resonator design to maximize signal sensitivity. images had a resolution of 100x78x78 mu m(3) with a signal-to-noise ratio per voxel greater than 25:1 and excellent contrast-to-noise ratios over a 30-min acquisition. We quantitatively validated the methods through comparisons of neuroanatomy across two lines of genetically engineered mice. Specifically, we were able to detect volumetric differences of as little as 9% between genetically engineered mouse strains in multiple brain regions that were predictive of underlying impairments in brain development. The. overall methodology was straightforward to implement and provides ready access to basic MRM at field strengths that are widely available in both the laboratory and the clinic. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:672 / 680
页数:9
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