Dynamic contrast-enhanced susceptibility-weighted perfusion MRI (DSC-MRI) in a glioma model of the rat brain using a conventional receive-only surface coil with a inner diameter of 47 mm at a clinical 1.5 T scanner

被引:14
|
作者
Ulmer, Stephan [1 ]
Reeh, Matthias [1 ]
Krause, Joerg [2 ]
Herdegen, Thomas [3 ]
Heldt-Feindt, Janka [2 ]
Jansen, Olav [1 ]
Rohr, Axel [1 ]
机构
[1] Univ Hosp Schleswig Holstein, Inst Neuroradiol, D-24105 Kiel, Germany
[2] Univ Hosp Schleswig Holstein, Mol Biol Sect, Dept Neurosurg, Kiel, Germany
[3] Univ Hosp Schleswig Holstein, Inst Pharmacol, Kiel, Germany
关键词
DSC-MRI; intracerebral tumor xenografts; clinical 1.5 T MR scanner;
D O I
10.1016/j.jneumeth.2008.04.022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Magnetic resonance (MR) imaging in animal models is usually performed in expensive dedicated small bore animal scanners of limited availability. In the present study a standard clinical 1.5T MR scanner was used for morphometric and dynamic contrast-enhanced susceptibility-weighted MR imaging (DSC-MRI) of a glioma model of the rat brain. Ten male Wistar rats were examined with coronal T2-weighted, and T1 -weighted images (matrix 128 x 128, FOV 64 mm) after implantation of an intracerebral tumor xenografts (C6) using a conventional surface coil. For DSC-MRI aT2*-weighted sequence TR/TE = 30/14 ins, matrix 64 x 64, FOV 90 mm; slice thickness of 1.5 mm) was performed. Regions of interest were defined within the tumor and the non-affected contralateral hemisphere and the mean transit time (MTT) was determined. Tumor dimensions in MR predicted well its real size as proven by histology. The MTT of contrast agent passing through the brain was significantly decelerated in the tumor compared to the unaffected hemisphere (p < 0.001, paired t-test), which is most likely due to the leakage of contrast agent through the disrupted blood brain barrier. This setup offers advanced MR imaging of small animals without the need for dedicated animal scanners or dedicated custom-made coils. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:168 / 172
页数:5
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