Wu Qi-Zhu, Yang Qing, Cate Holly S, Kemper Dennis, Binder Michele, Wang Hong-Xin, Fang Ke, Quick Melissa J, Marriott Mark, Kilpatrick Trevor J, Egan Gary F
Howard Florey Institute, University of Melbourne, Victoria, Australia.
J Magn Reson Imaging. 2008 Mar;27(3):446-53. doi: 10.1002/jmri.21111.
To characterize and compare histological and MRI-based changes within the corpus callosum (CC) in the cuprizone mouse model of multiple sclerosis (MS).
A total of 12 C57/BL6 mice were fed cuprizone from eight weeks of age for four weeks. One cohort of six cuprizone and two control mice were scanned with a T2-weighted (T2W) sequence. The other cohort of six cuprizone and four control mice were scanned using a dual-echo sequence for T2-mapping and a diffusion-weighted sequence with two orthogonal diffusion encoding directions to calculate water diffusivities parallel and perpendicular to the CC fiber (apparent diffusion coefficients ADC and ADC(perpendicular)). After the mice were killed, the rostral-caudal pattern of CC demyelination and other pathologies were examined using Luxol Fast Blue, neurofilament staining, and immunohistochemistry for microglia and were correlated with MRI.
In contrast to control mice, T2W imaging (T2WI) hyperintensity, reduced ADC(parallel), and elevated ADC(perpendicular) were detected in the CC of cuprizone-fed mice, particularly in the caudal segment. The T2 value was increased in the entire CC. Marked demyelination, as well as axonal injury, microglia accumulation, and cellular infiltration were found in the caudal section of the cuprizone mouse CC. The rostral-caudal pattern of abnormalities within the CC in MRI measurements correlated well with histopathological findings.
Noninvasive MRI using quantitative T2 and ADC mapping accurately characterized the rostral-caudal pattern of CC demyelination and other pathologies in cuprizone challenged mice, and thus could provide an effective way to assess the structural response to experimental therapeutics being designed for the treatment of MS.
在多发性硬化症(MS)的铜螯合剂小鼠模型中,对胼胝体(CC)内基于组织学和MRI的变化进行表征和比较。
总共12只C57/BL6小鼠从8周龄开始喂食铜螯合剂,持续4周。一组6只喂食铜螯合剂的小鼠和2只对照小鼠用T2加权(T2W)序列进行扫描。另一组6只喂食铜螯合剂的小鼠和4只对照小鼠使用双回波序列进行T2映射,并使用具有两个正交扩散编码方向的扩散加权序列来计算平行和垂直于CC纤维的水扩散率(表观扩散系数ADC和ADC(垂直))。在小鼠处死之后,使用卢氏固蓝、神经丝染色以及小胶质细胞免疫组织化学检查CC脱髓鞘和其他病理变化的头-尾模式,并与MRI进行关联。
与对照小鼠相比,在喂食铜螯合剂的小鼠的CC中检测到T2W成像(T2WI)高信号、ADC(平行)降低和ADC(垂直)升高,特别是在尾段。整个CC的T2值增加。在铜螯合剂小鼠CC的尾段发现明显的脱髓鞘以及轴突损伤、小胶质细胞积聚和细胞浸润。MRI测量中CC内异常的头-尾模式与组织病理学结果密切相关。
使用定量T2和ADC映射的无创MRI准确地表征了铜螯合剂攻击小鼠中CC脱髓鞘和其他病理变化的头-尾模式,因此可以提供一种有效的方法来评估针对MS设计的实验性治疗的结构反应。