Takahashi T, Takahashi K, Ido T, Yanai K, Iwata R, Ishiwata K, Nozoe S
Int J Appl Radiat Isot. 1985 Dec;36(12):965-9. doi: 10.1016/0020-708x(85)90257-1.
Five indolealkylamines (N,N-dimethyltryptamine, N-methyltryptamine, bufotenine, O-methylbufotenine, N,N,N-trimethyltryptamine iodide) were labeled with 11C by use of 11CH3I. The labeled compounds were synthesized with a radiochemical yield of 2-50% (based on trapped 11CH3I) in 20-35 min with radiochemical purities of more than 92%. The tissue distributions of these labeled compounds were investigated in rats. In all cases, the accumulations in the liver, lung and small intestine were high. [11C]DMT and [11C]OMB also accumulated to a large extent in the brain, where their accumulation was retained. Brain uptake of three other radiopharmaceuticals was low. [11C]DMT is the radiopharmaceutical of choice for the study of the serotonin action mechanism in the brain, because it has the highest radiochemical yield and the highest brain uptake of these 11C-labeled compounds.
使用11CH3I将五种吲哚烷基胺(N,N-二甲基色胺、N-甲基色胺、蟾毒色胺、O-甲基蟾毒色胺、碘化N,N,N-三甲基色胺)用11C进行标记。标记化合物在20 - 35分钟内合成,放射化学产率为2 - 50%(基于捕获的11CH3I),放射化学纯度超过92%。在大鼠中研究了这些标记化合物的组织分布。在所有情况下,肝脏、肺和小肠中的蓄积量都很高。[11C]DMT和[11C]OMB在大脑中也有大量蓄积,且其蓄积量保持不变。其他三种放射性药物在大脑中的摄取量较低。[11C]DMT是研究大脑中5-羟色胺作用机制的首选放射性药物,因为在这些11C标记的化合物中,它具有最高的放射化学产率和最高的大脑摄取量。