Madularu Dan, Mathieu Axel P, Kumaragamage Chathura, Reynolds Lauren M, Near Jamie, Flores Cecilia, Rajah M Natasha
Department of Psychiatry, Faculty of Medicine, McGill University, Montreal, QC, Canada; Brain Imaging Centre, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
Brain Imaging Centre, Douglas Mental Health University Institute, McGill University, Montreal, QC, Canada.
J Neurosci Methods. 2017 Aug 1;287:53-57. doi: 10.1016/j.jneumeth.2017.06.008. Epub 2017 Jun 17.
Preclinical neuroimaging allows for the assessment of brain anatomy, connectivity and function in laboratory animals, such as mice and rats. Most of these studies are performed under anesthesia to avoid movement during the scanning sessions.
Due to the limitations associated with anesthetized imaging, recent efforts have been made to conduct rodent imaging studies in awake animals, habituated to the restraint systems used in these instances. As of now, only one such system is commercially available for mouse scanning (Animal Imaging Research, Boston, MA, USA) integrating the radiofrequency coil electronics with the restraining element, an approach which, although effective in reducing head motion during awake imaging, has some limitations. In the current report, we present a novel mouse restraining system that addresses some of these limitations.
RESULTS/COMPARISON TO OTHER METHODS: The effectiveness of the restraining system was evaluated in terms of three-dimensional linear head movement across two consecutive functional MRI scans (total 20min) in 33 awake mice. Head movement was minimal, recorded in roughly 12% of the time-series. Respiration rate during the acclimation procedure dropped while the bolus count remained unchanged. Body movement during functional acquisitions did not have a significant effect on magnetic field (B) homogeneity.
CONCLUSION/NOVELTY: Compared to the commercially available system, the benefit of the current design is two-fold: 1) it is compatible with a range of commercially-available coils, and 2) it allows for the pairing of neuroimaging with other established techniques involving intracranial cannulation (i.e. microinfusion and optogenetics).
临床前神经成像可用于评估实验动物(如小鼠和大鼠)的脑解剖结构、连通性和功能。这些研究大多在麻醉状态下进行,以避免扫描过程中动物移动。
由于麻醉成像存在局限性,近期人们努力在清醒动物中开展啮齿动物成像研究,使动物适应此类情况下使用的约束系统。截至目前,仅有一款此类系统(美国马萨诸塞州波士顿的动物成像研究公司)可用于小鼠扫描,该系统将射频线圈电子设备与约束元件集成在一起,这种方法虽然在减少清醒成像过程中的头部运动方面有效,但存在一些局限性。在本报告中,我们介绍了一种新型小鼠约束系统,该系统解决了其中一些局限性。
结果/与其他方法的比较:在33只清醒小鼠连续两次功能性磁共振成像扫描(共20分钟)过程中,通过三维线性头部运动评估了约束系统的有效性。头部运动极小,在大约12%的时间序列中被记录到。适应过程中的呼吸频率下降,而团注计数保持不变。功能性采集过程中的身体运动对磁场(B)均匀性没有显著影响。
结论/新颖之处:与市售系统相比,当前设计的优点有两个:1)它与一系列市售线圈兼容;2)它允许将神经成像与其他涉及颅内插管的成熟技术(即微量注射和光遗传学)结合使用。