首页> 美国卫生研究院文献>Journal of Cerebral Blood Flow Metabolism >Kinetic modelling of 11CPBR28 for 18 kDa translocatorprotein PET data: A validation study of vascular modelling in the brain usingXBD173 and tissue analysis
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Kinetic modelling of 11CPBR28 for 18 kDa translocatorprotein PET data: A validation study of vascular modelling in the brain usingXBD173 and tissue analysis

机译:18 kDa易位分子11C PBR28的动力学建模蛋白PET数据:使用以下方法对大脑中的血管建模进行验证研究XBD173和组织分析

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摘要

The 18 kDa translocator protein (TSPO) is a marker of microglia activation in the central nervous system and represents the main target of radiotracers for the in vivo quantification of neuroinflammation with positron emission tomography (PET). TSPO PET is methodologically challenging given the heterogeneous distribution of TSPO in blood and brain. Our previous studies with the TSPO tracers [11C]PBR28 and [11C]PK11195 demonstrated that a model accounting for TSPO binding to the endothelium improves the quantification of PET data. Here, we performed a validation of the kinetic model with the additional endothelial compartment through a displacement study. Seven subjects with schizophrenia, all high-affinity binders, underwent two [11C]PBR28 PET scans before and after oral administration of 90 mg of the TSPO ligand XBD173. The addition of the endothelial component provided a signal compartmentalization much more consistent with the underlying biology, as only in this model, the blocking study produced the expected reduction in the tracer concentration of the specific tissue compartment, whereas the non-displaceable compartment remained unchanged. In addition, we also studied TSPO expression in vessels using 3D reconstructions of histological data offrontal lobe and cerebellum, demonstrating that TSPO positive vessels accountfor 30% of the vascular volume in cortical and white matter.
机译:18 kDa转运蛋白(TSPO)是中枢神经系统中小胶质细胞活化的标志物,是放射性示踪剂在正电子发射断层扫描(PET)体内定量定量神经炎症的主要目标。鉴于TSPO在血液和大脑中的分布不均,因此TSPO PET在方法上具有挑战性。我们先前对TSPO示踪剂[ 11 C] PBR28和[ 11 C] PK11195的研究表明,考虑TSPO与内皮结合的模型可改善PET数据的定量。在这里,我们通过位移研究对带有额外内皮区室的动力学模型进行了验证。在口服给予90 mg的TSPO配体XBD173之前和之后,对7位患有精神分裂症的受试者(均具有高亲和力)进行了两次[ 11 C] PBR28 PET扫描。内皮成分的添加提供了与基础生物学更加一致的信号区分开,因为仅在该模型中,阻断研究产生了特定组织区示踪剂浓度的预期降低,而不可移位区保持不变。此外,我们还使用3D组织学数据重建了血管中TSPO的表达。额叶和小脑,表明TSPO阳性血管占皮质和白质中30%的血管体积。

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