Goto S, Egashira T, Yamanaka Y
Department of Pharmacology, Medical College of Oita, Japan.
Jpn J Pharmacol. 1991 Jul;56(3):297-302. doi: 10.1254/jjp.56.297.
Addition of human cerebrospinal fluid (CSF) induced a marked inhibition of 3H-paroxetine binding to the monkey cortical membranes, while the specific binding of 3H-imipramine was slightly inhibited. Moreover, 3H-serotonin (5-hydroxy-tryptamine, 5-HT) uptake inhibition in the monkey cortical synaptosomes was also increased as the volume of added CSF was increased. Scatchard analysis of specific 3H-paroxetine binding with human CSF showed non-competitive kinetics, although CSF was competitive with 3H-imipramine binding. The inhibitory effect of human CSF on 5-HT uptake was non-competitive in nature. The endogenous substances in human CSF most probably act at the recognition site labeled with 3H-paroxetine. Moreover, occupation of this site by the endogenous substances is likely to inhibit the 5-HT uptake process.
添加人脑脊液(CSF)可显著抑制3H-帕罗西汀与猴皮质膜的结合,而3H-丙咪嗪的特异性结合则受到轻微抑制。此外,随着添加脑脊液体积的增加,猴皮质突触体中3H-5-羟色胺(5-羟色胺,5-HT)的摄取抑制也增加。用人体脑脊液对特异性3H-帕罗西汀结合进行Scatchard分析显示为非竞争性动力学,尽管脑脊液与3H-丙咪嗪结合具有竞争性。人脑脊液对5-HT摄取的抑制作用本质上是非竞争性的。人脑脊液中的内源性物质很可能作用于用3H-帕罗西汀标记的识别位点。此外,内源性物质占据该位点可能会抑制5-HT的摄取过程。