Molecular NeuroImaging, LLC, New Haven, Connecticut; and.
J Nucl Med. 2013 Oct;54(10):1760-7. doi: 10.2967/jnumed.113.119933. Epub 2013 Aug 22.
In vivo imaging of adenosine 2A receptors (A2A) in the brain has attracted significant interest from the scientific community, because studies have shown that dysregulation of these receptors is implicated in a variety of neurodegenerative and psychiatric disorders, including Parkinson and Huntington diseases. This work aimed to describe the kinetic properties, test-retest results, and dosimetry estimates of (123)I-MNI-420, a SPECT radiotracer for the in vivo imaging of A2A in the brain.
Nine healthy human subjects were enrolled in this study; 7 completed (123)I-MNI-420 brain SPECT studies, and 2 participated in whole-body planar imaging evaluating (123)I-MNI-420 biodistribution and dosimetry. For 3 of the brain SPECT studies, arterial blood was collected for invasive modeling. Noninvasive models were also explored, including Logan graphical analysis and simplified reference tissue models. Test-retest reliability was assessed in 4 subjects. To evaluate radiotracer biodistribution and dosimetry, serial whole-body images were acquired immediately after injection and at selected time points after injection. Urine samples were collected over a period of 21 h to calculate urinary excretion.
(123)I-MNI-420 rapidly entered the human brain and displayed uptake consistent with known A2A densities. At pseudoequilibrium (reached at 90 min after radiotracer injection), stable target-to-cerebellum ratios of around 1.4-2.0 were determined. Binding potentials around 0.8-1.2 were estimated using different kinetic models and the cerebellum as the reference region. Average test-retest variability in the striatum was 4.8%, 3.5%, and 6.5% for the simplified reference tissue model, Logan graphical analysis, and standardized uptake value ratio methods, respectively. The estimated radiation effective dose determined from whole-body studies was 0.036 mSv/MBq.
The data indicate that (123)I-MNI-420 is a useful SPECT radiotracer for imaging A2A in the brain and has radiation doses that would allow for multiple scans in the same research subject each year. The availability of (123)I-MNI-420 offers the possibility of investigating A2A activity in specific conditions and evaluating drug occupancy for A2A candidate therapeutics.
描述用于大脑中腺苷 A2A 受体(A2A)体内成像的放射性示踪剂(123)I-MNI-420 的动力学特性、重复测试结果和剂量估算。
本研究纳入了 9 名健康的人类受试者;其中 7 名完成了(123)I-MNI-420 脑 SPECT 研究,2 名参与了全身平面成像,评估(123)I-MNI-420 的生物分布和剂量估算。在 3 项脑 SPECT 研究中,采集了动脉血进行侵袭性建模。还探索了非侵袭性模型,包括 Logan 图形分析和简化参照组织模型。4 名受试者进行了重复测试可靠性评估。为了评估放射性示踪剂的生物分布和剂量估算,在注射后立即和注射后选定时间点采集了连续的全身图像。在 21 小时内收集尿液样本,以计算尿液排泄。
(123)I-MNI-420 迅速进入人体大脑,显示出与已知 A2A 密度一致的摄取。在放射性示踪剂注射后 90 分钟达到假性平衡时,确定了约 1.4-2.0 的稳定靶/小脑比率。使用不同的动力学模型和小脑作为参照区域,估计结合潜能约为 0.8-1.2。使用简化参照组织模型、Logan 图形分析和标准化摄取比值方法,纹状体的平均重复测试变异性分别为 4.8%、3.5%和 6.5%。全身研究确定的估计辐射有效剂量为 0.036 mSv/MBq。
数据表明,(123)I-MNI-420 是一种有用的 SPECT 放射性示踪剂,可用于大脑中 A2A 的成像,并且辐射剂量允许在同一位研究对象中每年进行多次扫描。(123)I-MNI-420 的可用性为研究特定条件下的 A2A 活性和评估 A2A 候选治疗药物的药物占有率提供了可能性。