Faculty of Radiological Technology, School of Medical Sciences, Fujita Health University, Japan.
Faculty of Radiological Technology, School of Medical Sciences, Fujita Health University, Japan.
Magn Reson Imaging. 2020 Sep;71:11-16. doi: 10.1016/j.mri.2020.05.001. Epub 2020 May 21.
The present study aimed to confirm the hypothesis that aquaporin-4 water channels (AQP4) control solute transition into the brain parenchyma using image analysis of gadolinium-based contrast agents (GBCAs) dissolved in cerebrospinal fluid (CSF) on dynamic contrast-enhanced magnetic resonance imaging (dyMRI) in live rats. Ten male Wistar ST rats were included in the study. Whole-brain dyMRI was performed for approximately 120 min after intrathecal infusion of gadolinium tetraazacyclododecane tetraacetic acid (Gd-DOTA). TGN-020, a specific AQP4 inhibitor, was used to inhibit the function of AQP4 in one group of rats (TGN-020 group, n = 4). The dyMRI after Gd-DOTA infusion in the rat, who were not treated with TGN-020 (control group, n = 6) revealed marked contrast-enhancement over time based on the distribution of the GBCA in the lateral regions of the brain surface, the ventral regions, the regions adjacent to the subarachnoid space, and the deep subcortical region. In contrast, smaller signal enhancement of the same regions in the TGN-020 group indicated poor distribution of the GBCA, suggesting a physiological consequence of the AQP4 inhibition by TGN-020. In this study, a close relationship between the function of AQP4 and the solute dynamics in the CSF was revealed from the distribution pattern of GBCA visualized in dyMRI in the living rat brain by administration of AQP4-selective inhibitor. This finding suggests that AQP4 functions to drive a glymphatic influx to transition molecules dissolved in the CSF from the subarachnoid space into the extracellular space of the brain parenchyma.
本研究旨在通过在活鼠大脑中进行动态对比增强磁共振成像(dyMRI),利用脑脊液(CSF)中溶解的钆基对比剂(GBCA)的图像分析,证实水通道蛋白-4(AQP4)水通道控制溶质向脑实质转运的假说。研究纳入 10 只雄性 Wistar ST 大鼠。在鞘内注射钆四氮杂环十二烷四乙酸(Gd-DOTA)后,对全脑 dyMRI 进行了大约 120 分钟的检测。使用 TGN-020(一种特定的 AQP4 抑制剂)抑制一组大鼠(TGN-020 组,n=4)的 AQP4 功能。未用 TGN-020 处理的大鼠(对照组,n=6)在 Gd-DOTA 输注后的 dyMRI 显示,GBCA 在脑表面外侧区域、腹侧区域、靠近蛛网膜下腔的区域和深皮质下区域的分布随时间推移呈现出明显的对比增强。相比之下,TGN-020 组相同区域的信号增强较小,表明 GBCA 分布不良,这表明 TGN-020 对 AQP4 的抑制作用产生了生理后果。在这项研究中,通过给予 AQP4 选择性抑制剂,在活鼠大脑的 dyMRI 中可视化 GBCA 的分布,揭示了 AQP4 功能与 CSF 中溶质动力学之间的密切关系。这一发现表明,AQP4 促进了从蛛网膜下腔到脑实质细胞外空间的溶解在 CSF 中的分子的糖质内流。