18F-GE-180: a novel TSPO radiotracer compared to 11C-R-PK11195 in a preclinical model of stroke

被引:100
作者
Boutin, Herve [1 ,2 ]
Murray, Katie [3 ]
Pradillo, Jesus [3 ]
Maroy, Renaud [4 ]
Smigova, Alison [2 ]
Gerhard, Alexander [1 ,2 ]
Jones, Paul A. [5 ]
Trigg, William [5 ]
机构
[1] Univ Manchester, Fac Med & Human Sci, Manchester M20 3LJ, Lancs, England
[2] Univ Manchester, Wolfson Mol Imaging Ctr, Manchester M20 3LJ, Lancs, England
[3] Univ Manchester, Fac Life Sci, Manchester M20 3LJ, Lancs, England
[4] CEA Orsay, SHFJ, Orsay, France
[5] GE Healthcare Ltd, Amersham, Bucks, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Positron emission tomography; Translocator protein; R-PK11195; Brain ischaemia; GE-180; FOCAL CEREBRAL-ISCHEMIA; PROTEIN; 18; KDA; MICROGLIAL ACTIVATION; SYSTEMIC INFLAMMATION; PARKINSONS-DISEASE; MULTIPLE-SCLEROSIS; PET LIGAND; ALZHEIMERS; NEUROINFLAMMATION; BINDING;
D O I
10.1007/s00259-014-2939-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Neuroinflammation plays a critical role in various neuropathological conditions, and hence there is renewed interest in the translocator protein (TSPO) as a biomarker of microglial activation and macrophage infiltration in the brain. This is reflected in the large amount of research conducted seeking to replace the prototypical PET radiotracer C-11-R-PK11195 with a TSPO ligand with higher performance. Here we report the in vivo preclinical investigation of the novel TSPO tracer F-18-GE-180 in a rat model of stroke. Focal cerebral ischaemia was induced in Wistar rats by 60-min occlusion of the middle cerebral artery (MCAO). Brain damage was assessed 24 h after MCAO by T2 MRI. Rats were scanned with C-11-R-PK11195 and F-18-GE-180 5 or 6 days after MCAO. Specificity of binding was confirmed by injection of unlabelled R-PK11195 or GE-180 20 min after injection of F-18-GE-180. In vivo data were confirmed by ex vivo immunohistochemistry for microglial (CD11b) and astrocytic biomarkers (GFAP). F-18-GE-180 uptake was 24 % higher in the core of the ischaemic lesion and 18 % lower in the contralateral healthy tissue than that of C-11-R-PK11195 uptake (1.5 +/- 0.2-fold higher signal to noise ratio). We confirmed this finding using the simplified reference tissue model (BPND = 3.5 +/- 0.4 and 2.4 +/- 0.5 for F-18-GE-180 and C-11-R-PK11195, respectively, with R (1) = 1). Injection of unlabelled R-PK11195 or GE-180 20 min after injection of F-18-GE-180 significantly displaced F-18-GE-180 (69 +/- 5 % and 63 +/- 4 %, respectively). Specificity of the binding was also confirmed by in vitro autoradiography, and the location and presence of activated microglia and infiltrated macrophages were confirmed by immunohistochemistry. The in vivo binding characteristics of F-18-GE-180 demonstrate a better signal to noise ratio than C-11-R-PK11195 due to both a better signal in the lesion and lower nonspecific binding in healthy tissue. These results provide evidence that F-18-GE-180 is a strong candidate to replace C-11-R-PK11195.
引用
收藏
页码:503 / 511
页数:9
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