[11C]DAA1106:: Radiosynthesis and in vivo binding to peripheral benzodiazepine receptors in mouse brain

被引:140
作者
Zhang, MR
Kida, T
Noguchi, J
Furutsuka, K
Maeda, J
Suhara, T
Suzuki, K
机构
[1] Natl Inst Radiol Sci, Dept Med Imaging, Inage Ku, Chiba 2638555, Japan
[2] SHI Accelerator Serv Co Ltd, Tokyo 1418686, Japan
[3] Japan Sci & Technol Corp, CREST, Kawaguchi 3320012, Japan
关键词
peripheral benzodiazepine receptor; PBR; carbon-11; DAA; 1106; PET;
D O I
10.1016/S0969-8051(03)00016-7
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
DAA1106 (N-(2,5-Dimethoxybenzyl)-N-(5-fluoro-2-phenoxyphenyl)acetamide), is a potent and selective ligand for peripheral benzodiazepine receptors (PBR) in mitochondrial fractions of rat (K-i=0.043 nM) and monkey (K-i=0.188 nM) brains. This compound was labeled by [C-11]methylation of a corresponding desmethyl precursor (DAA1123) with [C-11]CH3I in the presence of NaH, with a 72+/-16% (corrected for decay) incorporation yield of radioactivity. After HPLC purification, [C-11]DAA1106 was obtained with 98% radiochemical purity and specific activity of 90-156 GBq/mumol at the end of synthesis. After iv injection of [C-11]DAA1106 into mice, high accumulations of radioactivity were found in the olfactory bulb and cerebellum, the high PBR density regions in the brain. Coinjection of [C-11]DAA1106 with unlabeled DAA1106 and PBR-selective PK11195 displayed a significant reduction of radioactivity, suggesting a high specific binding of [C-11]DAA1106 to PBR. Although this tracer was rapidly metabolized in the plasma, only [C-11]DAA1106 was detected in the brain tissues, suggesting the specific binding in the brain due to the tracer itself. These findings revealed that [C-11]DAA1106 is a potential and selective positron emitting radioligand for PBR. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:513 / 519
页数:7
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