Synthesis and in vivo evaluation of [11C]zolpidem, an imidazopyridine with agonist properties at central benzodiazepine receptors

被引:17
作者
Dumont, F
Waterhouse, RN
Montoya, JA
Mattner, F
Katsifis, A
Kegeles, LS
Laruelle, M
机构
[1] Columbia Univ, Dept Psychiat, New York, NY 10032 USA
[2] Columbia Univ, Dept Radiol, New York, NY 10032 USA
[3] ANSTO, PMBI, Menai, NSW, Australia
关键词
central benzodiazepine receptors; agonist; C-11]zolpidem; PET;
D O I
10.1016/S0969-8051(03)00006-4
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
The synthesis and evaluation of [C-11]zolpidem, an imidazopyridine with agonist properties at central benzodiazepine receptors, is reported herein. The reaction of desmethylzolpidem with [C-11] methyl iodide afforded the title compound [C-11]zolpidem in a yield of 19.19 +/- 3.23% in 41 +/- 2 min in specific activities of 0.995-1.19 Ci/mumol (1.115 +/- 0.105 Ci/mumol) (n = 3; decay corrected, EOB). The amount of radioactivity in the brain after tail vein injection in male Wistar rats was low, and the regional distribution was homogeneous and not consistent with the known distribution of the central benzodiazepine receptors. The frontal cortex/cerebellum ratio was not significantly greater than one (1.007 +/- 0.266 at 5 min) and did not increase from 5 to 40 min post-injection. A PET brain imaging study in one baboon confirmed the results obtained in rats. Therefore, it can be concluded that [C-11]zolpidem is not a suitable tracer for in vivo visualization of central benzodiazepine receptors. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:435 / 439
页数:5
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