IBZM SPECT IMAGING OF STRIATAL DOPAMINE-2 RECEPTORS IN PSYCHOTIC-PATIENTS TREATED WITH THE NOVEL ANTIPSYCHOTIC SUBSTANCE QUETIAPINE IN COMPARISON TO CLOZAPINE AND HALOPERIDOL
B. Kufferle et al., IBZM SPECT IMAGING OF STRIATAL DOPAMINE-2 RECEPTORS IN PSYCHOTIC-PATIENTS TREATED WITH THE NOVEL ANTIPSYCHOTIC SUBSTANCE QUETIAPINE IN COMPARISON TO CLOZAPINE AND HALOPERIDOL, Psychopharmacology, 133(4), 1997, pp. 323-328
We investigated the striatal dopamine-2 (D-2) receptor occupancy cause
d by different antipsychotic substances in 18 psychotic patients (16 w
ith schizophrenic and two with schizoaffective disorder according to D
SM-TV) with single photon emission computed tomography (SPECT) using I
-123-iodobenzamide (IBZM) as tracer substance. Four patients were trea
ted with the novel antipsychotic compound quetiapine (300-700 mg/day),
six with clozapine (300-600 mg/ day) and eight with haloperidol (10-2
0 mg/day). They were compared with eight healthy controls. Measurement
of S/F ratios and consecutive calculation of D-2 receptor occupancy r
evealed a significantly lower striatal D-2 occupancy rate with quetiap
ine and clozapine in comparison to haloperidol. In correspondence with
the low striatal D-2 receptor occupancy rates and again in contrast t
o the haloperidol treatment group, there were no extrapyramidal motor
side-effects (EPS) in the quetiapine and clozapine treatment groups. T
herefore, the reported data support the position that quetiapine can b
e considered to be an atypical antipsychotic substance due to its rela
tively weak striatal D-2 receptor blocking property and therefore its
low propensity to induce EPS.