Arnett C D, Fowler J S, Wolf A P, MacGregor R R
J Neurochem. 1983 Feb;40(2):455-9. doi: 10.1111/j.1471-4159.1983.tb11304.x.
Spiroperidol labeled with carbon-11, a short-lived positron-emitting radionuclide, was used to determine the time course of specific binding of this radioligand to the neuroleptic receptor in vivo in the rat. The three major bran pools--specifically bound, nonspecifically bound, and free (unbound)--were determined over a 60-mm time course by a rapid filtration technique, utilizing (-)- and (+)-butaclamol pretreatments to assess total and nonspecifically bound activities, respectively, in striatum and cerebellum. The ratio of specifically to nonspecifically bound pools in the striatum was 4.1 at 30 min and 5.1 at 60 min. Thus [11C]spiroperidol may be useful for labeling neuroleptic receptors in vivo for serial studies using positron emission transaxial tomography.
用碳 -11 标记的螺哌利多(一种半衰期短的发射正电子的放射性核素)来测定这种放射性配体在大鼠体内与抗精神病药物受体特异性结合的时间进程。通过快速过滤技术,在 60 分钟的时间进程内测定了三个主要的放射性活度库——特异性结合、非特异性结合和游离(未结合)的放射性活度库,利用(-)-和(+)-布他拉莫预处理分别评估纹状体和小脑中的总放射性活度和非特异性结合的放射性活度。纹状体中特异性结合与非特异性结合库的比率在 30 分钟时为 4.1,在 60 分钟时为 5.1。因此,[11C]螺哌利多可能有助于在体内标记抗精神病药物受体,以便使用正电子发射断层扫描进行系列研究。