Time course of central nervous dopamine-D2 and 5-HT2 receptor blockade and plasma drug concentrations after discontinuation of quetiapine (Seroquel®) in patients with schizophrenia

Quetiapine (Seroquel) is a novel antipsychotic with an atypical profile in animal models and a relatively short plasma half-life of 2.5-5 h. In the present study, we used PET to compare the time course of blockade of dopamine D-2 and serotonin 5HT(2) receptors of quetiapine using C-11-raclopride and C-11-N-methyl-spiperone as ligands, parallel to monitoring plasma drug concentrations. It was an open study in 11 schizophrenic men using a fixed dose of 450 mg quetiapine. Eight men completed the 29 days treatment, followed by four PET scans performed over a 26-h period after withdrawal of the compound. Quetiapine was shown to bind to dopamine D-2 receptors in striatum and 2 h (t(max)) after the last dose, 44% receptor occupancy was calculated. After 26 h it had dropped to the same level as was found in untreated healthy volunteers. Serotonin 5HT(2) receptor blockade in the frontal cortex was 72% after 2 h, which declined to 50% after 26 h. The terminal plasma half-life of quetiapine was 5.3 h, Clinically, our eight patients had good antipsychotic effect without any extrapyramidal side-effects. Out-data shows that quetiapine has a relatively low affinity for dopamine D-2 receptors, with an occupancy half-life (10 h), which was about twice as long as that for plasma. A more prolonged blockade of the serotonin 5HT(2) receptors was found in the frontal cortex, with receptor occupancy half-life of 27 h. Compared to clozapine as demonstrated in other studies, quetiapine has much the same ratio of D-2/5HT(2) occupancy. This could suggest that the combination of D-2/5HT(2) receptor blockade contributes to the antipsychotic effect and a low incidence of EPS seen with quetiapine in comparative phase three trials. Our results also confirm the clinical data that quetiapine ran be administered twice daily.