Centre de Résonance Magnétique des Systèmes biologiques, UMR 5536, CNRS/Université Victor Segalen Bordeaux 2, 146, rue Léo Saignat 33076 Bordeaux Cedex, France.
Contrast Media Mol Imaging. 2011 Jul-Aug;6(4):275-81. doi: 10.1002/cmmi.429. Epub 2011 Feb 2.
A specific mouse whole body coil and a dedicated gradient system at 4.7 T were coupled with an ultra-fast 3D gradient echo MRI and keyhole reconstruction technique to obtain 3D whole-body dynamic T(1)-weighted or T(2)-weighted imaging. The technique was used to visualize the real-time distribution of non-targeting T(1) and T(2) contrast agent (CA) in a glioma-bearing mouse model. T(1) dynamic contrast-enhancement imaging was performed with a fast imaging with steady-state precession sequence [echo time/repetition time (TE/TR), 1.32/3.7 ms] before and after CA injection (Gd-DOTA and BSA-Gd-DOTA) for 21 min. The temporal resolution was 1 image/6.5 s. T(2)* imaging (TE/TR, 4/8 ms) was performed before and after iron-based (small and ultra-small particles of iron oxide) CA injection for 45 min. The temporal resolution was 1 image/14 s. Signal-to-noise ratio curves were determined in various mouse organs. The whole-body coil and gradient systems made it possible to acquire data with sufficient and homogeneous signal-to-noise ratio on the whole animal. The spatial resolution allowed adequate depiction of the major organs, blood vessels and brain glioma. The distribution and the time-course of T(1) and T(2)* contrasts upon contrast agent injection were also assessed. 3D whole-body mouse MRI is feasible at high spatial resolution in movie mode and can be applied successfully to visualize real-time contrast agent distribution. This method should be effective in future preclinical molecular imaging studies.
特定的小鼠全身线圈和 4.7T 专用梯度系统与超快 3D 梯度回波 MRI 和关键孔重建技术相结合,可获得 3D 全身动态 T(1)加权或 T(2)*加权成像。该技术用于可视化非靶向 T(1)和 T(2)*造影剂(CA)在荷胶质瘤小鼠模型中的实时分布。在 CA 注射(Gd-DOTA 和 BSA-Gd-DOTA)前后,使用快速稳态进动序列[回波时间/重复时间(TE/TR),1.32/3.7ms]进行 T(1)动态对比增强成像,持续 21 分钟。时间分辨率为 1 幅图像/6.5s。在 CA 注射前后(小氧化铁和超小氧化铁颗粒)进行 T(2)*成像(TE/TR,4/8ms),持续 45 分钟。时间分辨率为 1 幅图像/14s。在各种小鼠器官中确定了信噪比曲线。全身线圈和梯度系统使在整个动物上获得具有足够和均匀信噪比的数据成为可能。空间分辨率允许充分描述主要器官、血管和脑胶质瘤。还评估了 CA 注射后 T(1)和 T(2)*对比的分布和时间过程。高空间分辨率的 3D 全身小鼠 MRI 是可行的,可在电影模式下成功应用于可视化实时造影剂分布。这种方法在未来的临床前分子成像研究中应该是有效的。