Bahrani Ahmed A, Dundon Stephen R, Gao TianYu, Gant Christopher J, Kimseng Rungruedee, Gollihue Jenna L, Rogers Colin B, Weiss Blaine E, Sompol Pradoldej, Powel David K, Norris Christopher M
Department of Neurology, University of Kentucky, Lexington, KY, United States; Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, United States.
Magnetic Resonance Imaging and Spectroscopy Center, University of Kentucky, Lexington, KY, United States.
J Neurosci Methods. 2025 Jun 30;422:110525. doi: 10.1016/j.jneumeth.2025.110525.
Cerebral blood perfusion (CBP) plays a vital role in delivering oxygen and essential nutrients to support neuronal activity. Researchers commonly use mouse models with magnetic resonance imaging (MRI) to study CBP and brain function. However, a major challenge in these studies is the use of anesthesia, which significantly alters cerebrovascular dynamics and metabolic activity.
A 3D-printed, custom-designed frame and head mounting plate were used with an existing Bruker mouse cradle. To evaluate the repeatability of CBP measurements in awake versus anesthetized conditions, we used a flow-sensitive alternating inversion recovery (FAIR) sequence on a wild-type mouse that underwent a three-day training before scanning to acclimate it to the MRI environment.
CBP was significantly higher under anesthesia than in the awake condition for both the whole brain and cortex (P < 0.001). Under anesthesia, the mean perfusion for was 70.9 ± 5.6 ml/min/100 g for the whole brain and 67.8 ± 8.5 ml/min/100 g for just the cortex. Under awake conditions, the whole brain perfusion was 51.1 ± 3.3 ml/min/100 g and 46.7 ± 3.4 ml/min/100 g for the cortex. Perfusion variability, measured by variance and standard deviation, was consistently higher under anesthesia.
We built a unique mouse head stabilizing system for MRI and are the first to have specifically focused on CBP during awake conditions.
Our findings confirm that anesthesia significantly increases CBP, affecting the accuracy, reproducibility and relevance of perfusion-related studies. Accordingly, we developed a practical, MRI-compatible setup for imaging awake mice and used it to measure perfusion for more reliable neuroimaging research.
脑血流灌注(CBP)在输送氧气和必需营养物质以支持神经元活动方面起着至关重要的作用。研究人员通常使用磁共振成像(MRI)小鼠模型来研究CBP和脑功能。然而,这些研究中的一个主要挑战是使用麻醉,这会显著改变脑血管动力学和代谢活动。
将一个3D打印的、定制设计的框架和头部固定板与现有的布鲁克小鼠摇篮配合使用。为了评估清醒与麻醉条件下CBP测量的可重复性,我们在一只野生型小鼠上使用了流动敏感交替反转恢复(FAIR)序列,该小鼠在扫描前经过了三天的训练,以使其适应MRI环境。
全脑和皮层在麻醉状态下的CBP均显著高于清醒状态(P < 0.001)。在麻醉状态下,全脑平均灌注为70.9±5.6 ml/min/100 g,仅皮层为67.8±8.5 ml/min/100 g。在清醒条件下,全脑灌注为51.1±3.3 ml/min/100 g,皮层为46.7±3.4 ml/min/100 g。通过方差和标准差测量的灌注变异性在麻醉状态下始终较高。
我们构建了一个独特的用于MRI的小鼠头部稳定系统,并且是首个专门关注清醒状态下CBP的研究。
我们的研究结果证实,麻醉会显著增加CBP,影响灌注相关研究的准确性、可重复性和相关性。因此,我们开发了一种实用的、与MRI兼容的用于清醒小鼠成像的装置,并使用它来测量灌注,以进行更可靠的神经影像学研究。