phencyclidine (PCP);
4-phenyl-4-(1-piperidinyl)cyclohexanol (4-PPC);
serotonin uptake;
rat brain;
D O I:
10.1016/0304-3940(96)11617-7
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The effects of phencyclidine (PCP) and its metabolites on serotonin (5-hydroxytryptamine, 5-HT) receptors were studied. PCP and its metabolites inhibited the uptake of [H-3]5-HT and the binding of [H-3]paroxetine in rat brain, while they failed to inhibit either [H-3]5-HT binding to 5-HT1 receptors or [3H]ketanserin binding to 5-HT2 receptors. The trans-isomer of 4-phenyl-4-(1-piperidinyl)cyclohexanol (trans-4-PPC), the major metabolite of PCP, rather than PCP itself, inhibited [H-3]5-HT uptake most potently. These results suggest that the serotonergic effects of PCP, in part, may be based on the effects of PCP metabolites on 5-HT uptake.