Andorn A C
Life Sci. 1986 Apr 7;38(14):1251-60. doi: 10.1016/0024-3205(86)90417-0.
[3H]-Spiroperidol binds at several specific sites in postmortem human prefrontal cortex at 21 degrees C. The overall selectivity of these sites is serotonergic. At 37 degrees C, there is a marked loss of specific [3H]-spiroperidol binding that occurs between 10 and 60 min. This loss of binding is not apparently due to 3H-ligand degeneration or metabolism, or to non-specific binding site degradation. The loss of binding can also be produced by serotonin (5-HT), haloperidol and chlorpromazine but not by prazosin. The rate of the loss of binding is dependent on 3H-ligand concentration and protein concentration. The loss of binding is correlated with a loss of serotonin selective [3H]-spiroperidol binding sites having a KD of approximately 0.04 nM. Therefore antipsychotic compounds and 5-HT appear to down-regulate a subset of antipsychotic binding sites in human prefrontal cortex.
在21摄氏度时,[3H]-螺哌啶醇可结合于死后人类前额叶皮质的多个特定位点。这些位点的总体选择性是血清素能的。在37摄氏度时,在10至60分钟之间会出现明显的特异性[3H]-螺哌啶醇结合丧失。这种结合丧失显然不是由于3H-配体变性或代谢,也不是由于非特异性结合位点降解。血清素(5-HT)、氟哌啶醇和氯丙嗪也可导致结合丧失,但哌唑嗪不会。结合丧失的速率取决于3H-配体浓度和蛋白质浓度。结合丧失与具有约0.04 nM解离常数(KD)的血清素选择性[3H]-螺哌啶醇结合位点丧失相关。因此,抗精神病化合物和5-HT似乎会下调人类前额叶皮质中一部分抗精神病结合位点。