Marcinkiewicz M, Vergé D, Gozlan H, Pichat L, Hamon M
Brain Res. 1984 Jan 16;291(1):159-63. doi: 10.1016/0006-8993(84)90664-4.
The distribution of the binding sites of a new, potent agonist of serotonin (5-HT), 8-OH-N,N-dipropyl-2-aminotetralin (PAT), was studied in the rat brain with the quantitative autoradiographic technique utilizing tritium-sensitive LKB film. The localization of [3H]PAT binding sites was very similar to that of [3H]5-HT binding sites, except in some discrete regions (choroid plexus, striatum, area preoptica lateralis, subiculum, and substantia nigra), which exhibited very low levels of labeling with [3H]PAT and high levels with [3H]5-HT. These results indicate that 5-HT1 receptors are heterogeneous, and that [3H]PAT recognizes only a 5-HT1 subclass (called 5-HT1A).
利用对氚敏感的LKB胶片定量放射自显影技术,在大鼠脑中研究了一种新型强效血清素(5-羟色胺,5-HT)激动剂8-羟基-N,N-二丙基-2-氨基四氢萘(PAT)结合位点的分布。[3H]PAT结合位点的定位与[3H]5-HT结合位点非常相似,除了一些离散区域(脉络丛、纹状体、外侧视前区、海马下脚和黑质),这些区域用[3H]PAT标记的水平非常低,而用[3H]5-HT标记的水平很高。这些结果表明5-HT1受体是异质性的,并且[3H]PAT仅识别5-HT1亚类(称为5-HT1A)。