Department of Molecular Imaging and Theranostics, Institute for Quantum Medical Science, National Institute for Quantum and Radiological Science and Technology, 4-9-1 Anagawa, Inage-ku, Chiba, 263-8555, Japan.
Department of Functional Brain Imaging, Institute for Quantum Medical Science, National Institute for Quantum and Radiological Science and Technology, 4-9-1 Anagawa, Inage-ku, Chiba, 263-8555, Japan.
Ann Nucl Med. 2021 Aug;35(8):955-965. doi: 10.1007/s12149-021-01633-4. Epub 2021 Jun 8.
Positron emission tomography (PET) has been used to investigate changes in the concentration of endogenous neurotransmitters. Recently, this technique has been applied to the imaging of serotonin receptors using [F]altanserin. In these measurements, a reduction in binding potential (BP) suggests an increase in endogenous serotonin levels caused by pharmacological or cognitive stimulations, and the sensitivity of BP reduction depends on the characteristics of [F]altanserin. In this study, we evaluated an analytical method for estimating the changes in endogenous serotonin levels based on PET scans with [F]altanserin at baseline and stimulated states and validated it using simulations and small animal PET studies.
First, in the simulations, the time-activity curves at baseline and the stimulated states were generated using an extended compartment model including the competition for the receptors between the administered [F]altanserin and endogenous serotonin. In the stimulated state, the magnitude and onset of the endogenous serotonin elevation were altered to varying degrees. In these time-activity curves, BP was estimated using the simplified reference tissue model (SRTM), and the reduction in BP was evaluated by comparison with that of the baseline state. Next, the proposed method was applied to mouse PET studies. Endogenous serotonin levels were elevated by treatment with selective serotonin reuptake inhibitors (SSRIs), and PET studies were performed twice, once with and once without treatment. In both scans, BP was estimated using the SRTM with the cerebellum as a reference region, and the reduction in BP after SSRI treatment was evaluated.
In the simulations, the BP estimate of the stimulated state was smaller than that of the baseline state, and their reduction was related to the amount of change in the serotonin concentration. BP reduction was also affected by the onset of serotonin elevation. In the mouse studies, the BP of the cerebral cortex decreased in the scans with SSRI treatment.
The reduction in BP estimated using the SRTM from [F]altanserin-PET studies at baseline and in stimulated states can detect changes in the binding conditions of serotonin receptors. This may be useful for investigating the elevation of endogenous serotonin levels caused by stimulations.
正电子发射断层扫描(PET)已被用于研究内源性神经递质浓度的变化。最近,这项技术已被应用于使用[F]altanserin 对 5-羟色胺受体进行成像。在这些测量中,结合潜力(BP)的降低表明内源性 5-羟色胺水平因药理学或认知刺激而升高,BP 降低的敏感性取决于[F]altanserin 的特性。在这项研究中,我们评估了一种基于基线和刺激状态下使用[F]altanserin 的 PET 扫描估计内源性 5-羟色胺水平变化的分析方法,并通过模拟和小动物 PET 研究对其进行了验证。
首先,在模拟中,使用包括内源性 5-羟色胺与给予的[F]altanserin 之间受体竞争的扩展隔室模型生成基线和刺激状态下的时间-活性曲线。在刺激状态下,内源性 5-羟色胺升高的幅度和起始时间会发生不同程度的改变。在这些时间-活性曲线中,使用简化参考组织模型(SRTM)估计 BP,并通过与基线状态进行比较来评估 BP 的降低。接下来,将提出的方法应用于小鼠 PET 研究。通过使用选择性 5-羟色胺再摄取抑制剂(SSRIs)治疗来升高内源性 5-羟色胺水平,并进行两次 PET 扫描,一次有治疗,一次没有治疗。在两次扫描中,均使用小脑作为参考区域的 SRTM 估计 BP,并评估 SSRIs 治疗后的 BP 降低。
在模拟中,刺激状态下的 BP 估计值小于基线状态下的估计值,且其降低与 5-羟色胺浓度变化量有关。BP 降低也受 5-羟色胺升高起始时间的影响。在小鼠研究中,在有 SSRIs 治疗的扫描中,大脑皮层的 BP 降低。
使用 SRTM 从基线和刺激状态下的[F]altanserin-PET 研究中估计的 BP 降低可检测 5-羟色胺受体结合条件的变化。这可能有助于研究刺激引起的内源性 5-羟色胺水平升高。