Tóth Miklós, Doorduin Janine, Häggkvist Jenny, Varrone Andrea, Amini Nahid, Halldin Christer, Gulyás Balázs
Department of Clinical Neuroscience, Karolinska Institutet, Centrum for Psychiatry Research, Stockholm, Sweden.
Department of Clinical Neuroscience, Karolinska Institutet, Centrum for Psychiatry Research, Stockholm, Sweden; Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
PLoS One. 2015 May 21;10(5):e0125917. doi: 10.1371/journal.pone.0125917. eCollection 2015.
Molecular imaging of the 18 kD Translocator protein (TSPO) with positron emission tomography (PET) is of great value for studying neuroinflammation in rodents longitudinally. Quantification of the TSPO in rodents is, however, quite challenging. There is no suitable reference region and the use of plasma-derived input is not an option for longitudinal studies. The aim of this study was therefore to evaluate the use of the standardized uptake value (SUV) as an outcome measure for TSPO imaging in rodent brain PET studies, using [11C]PBR28. In the first part of the study, healthy male Wistar rats (n = 4) were used to determine the correlation between the distribution volume (VT, calculated with Logan graphical analysis) and the SUV. In the second part, healthy male Wistar rats (n = 4) and healthy male C57BL/6J mice (n = 4), were used to determine the test-retest variability of the SUV, with a 7-day interval between measurements. Dynamic PET scans of 63 minutes were acquired with a nanoScan PET/MRI and nanoScan PET/CT. An MRI scan was made for anatomical reference with each measurement. The whole brain VT of [11C]PBR28 in rats was 42.9 ± 1.7. A statistically significant correlation (r2 = 0.96; p < 0.01) was found between the VT and the SUV. The test-retest variability in 8 brain region ranged from 8 to 20% in rats and from 7 to 23% in mice. The interclass correlation coefficient (ICC) was acceptable to excellent for rats, but poor to acceptable for mice.
The SUV of [11C]PBR28 showed a high correlation with VT as well as good test-retest variability. For future longitudinal small animal PET studies the SUV can thus be used to describe [11C]PBR28 uptake in healthy brain tissue. Based on the present observations, further studies are needed to explore the applicability of this approach in small animal disease models, with special regard to neuroinflammatory models.
利用正电子发射断层扫描(PET)对18 kD转位蛋白(TSPO)进行分子成像,对于纵向研究啮齿动物的神经炎症具有重要价值。然而,对啮齿动物体内的TSPO进行定量分析颇具挑战性。目前尚无合适的参考区域,且对于纵向研究而言,使用血浆衍生输入并非可行之选。因此,本研究旨在评估标准化摄取值(SUV)作为啮齿动物脑PET研究中TSPO成像的一项结果指标的应用情况,采用的示踪剂为[11C]PBR28。在研究的第一部分,使用健康雄性Wistar大鼠(n = 4)来确定分布容积(VT,通过Logan图形分析法计算得出)与SUV之间的相关性。在第二部分,使用健康雄性Wistar大鼠(n = 4)和健康雄性C57BL/6J小鼠(n = 4)来确定SUV的重测变异性,测量间隔为7天。使用nanoScan PET/MRI和nanoScan PET/CT进行63分钟的动态PET扫描。每次测量时均进行MRI扫描以获取解剖学参考。大鼠脑中[11C]PBR28的全脑VT为42.9 ± 1.7。在VT与SUV之间发现了具有统计学意义的相关性(r2 = 0.96;p < 0.01)。在8个脑区中,大鼠的重测变异性范围为8%至20%,小鼠为7%至23%。大鼠的组内相关系数(ICC)为可接受至优秀,但小鼠的ICC为差至可接受。
[11C]PBR28的SUV与VT高度相关,且重测变异性良好。因此,对于未来的纵向小动物PET研究,SUV可用于描述健康脑组织中[11C]PBR28的摄取情况。基于目前的观察结果,需要进一步研究以探索该方法在小动物疾病模型中的适用性,尤其是在神经炎症模型方面。