首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Temporal Changes in In Vivo Glutamate Signal during Demyelination and Remyelination in the Corpus Callosum: A Glutamate-Weighted Chemical Exchange Saturation Transfer Imaging Study
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Temporal Changes in In Vivo Glutamate Signal during Demyelination and Remyelination in the Corpus Callosum: A Glutamate-Weighted Chemical Exchange Saturation Transfer Imaging Study

机译:在胼callosum中脱髓鞘和髓鞘中的体内谷氨酸信号中的时间变化:谷氨酸加权化学交换饱和转移成像研究

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摘要

Background: Glutamate-weighted chemical exchange saturation transfer (GluCEST) is a useful imaging tool that can be used to detect changes in glutamate levels in vivo and could also be helpful in the diagnosis of brain myelin changes. We investigated glutamate level changes in the cerebral white matter of a rat model of cuprizone-administered demyelination and remyelination using GluCEST. Method: We used a 7 T pre-clinical magnetic resonance imaging (MRI) system. The rats were divided into the normal control (CTRL), cuprizone-administered demyelination (CPZDM), and remyelination (CPZRM) groups. GluCEST data were analyzed using the conventional magnetization transfer ratio asymmetry in the corpus callosum. Immunohistochemistry and transmission electron microscopy analyses were also performed to investigate the myelinated axon changes in each group. Results: The quantified GluCEST signals differed significantly between the CPZDM and CTRL groups (−7.25 ± 1.42% vs. −2.84 ± 1.30%; p = 0.001). The increased GluCEST signals in the CPZDM group decreased after remyelination (−6.52 ± 1.95% in CPZRM) to levels that did not differ significantly from those in the CTRL group (p = 0.734). Conclusion: The apparent temporal signal changes in GluCEST imaging during demyelination and remyelination demonstrated the potential usefulness of GluCEST imaging as a tool to monitor the myelination process.
机译:背景技术:谷氨酸加权化学交换饱和度转移(葡萄糖)是一种有用的成像工具,可用于检测体内谷氨酸水平的变化,并且也有助于脑髓鞘的诊断变化。我们调查了使用葡萄糖抑制的脱髓鞘的大鼠模型的脑白物变化的谷氨酸水平变化。方法:我们使用了7吨前临床磁共振成像(MRI)系统。将大鼠分为正常对照(CTRL),铜沸酮施用的脱髓鞘(CPZDM)和重新髓鞘(CPZRM)组。使用肠道胼callosum中的常规磁化转移比不对称分析葡萄糖数据。还进行免疫组织化学和透射电子显微镜分析,以研究各组的肌肉轴突变化。结果:CPZDM和CTRL组之间量化的葡糖信号在显着不同(-7.25±1.42%,与-2.84±1.30%; p = 0.001)。 CPZDM组中的增加的葡萄糖信号在重新髓鞘(-6.52±1.95%的CPZRM中)降低到CTRL组中没有显着差异的水平(P = 0.734)。结论:脱髓鞘和重新髓鞘中的葡萄糖成像中的表观时间信号变化表明了葡萄质节成像作为监测髓鞘髓鞘过程的工具的潜在有用性。

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