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Am J Psychiatry 164:1411-1417, September 2007
doi: 10.1176/appi.ajp.2007.06091479
© 2007 American Psychiatric Association
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* Schizophrenia Spectrum Disorders
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* PET
*Related Article

Differential Effects of Aripiprazole on D2, 5-HT2, and 5-HT1A Receptor Occupancy in Patients With Schizophrenia: A Triple Tracer PET Study

David Mamo, M.D., M.Sc., Ariel Graff, M.D., Ph.D., Romina Mizrahi, M.D., Ph.D., C. M. Shammi, M.D., Françoise Romeyer, Ph.D., and Shitij Kapur, M.D., Ph.D.

OBJECTIVE: Aripiprazole has a unique pharmacological profile that includes partial agonism at D2 receptors, antagonism at 5-HT2 receptors, and partial agonism at 5-HT1A receptors. The authors conducted a positron emission tomography (PET) study to characterize the simultaneous effects of aripiprazole at the D2, 5-HT2, and 5-HT1A receptors in patients with schizophrenia or schizoaffective disorder. METHOD: Twelve patients who had previously received antipsychotic treatment were randomly assigned to receive 10 mg, 15 mg, 20 mg, or 30 mg of aripiprazole. After at least 14 days of treatment, participants underwent high-resolution PET scans using [11C]raclopride, [18F]setoperone, and [11C]WAY100635. RESULTS: Very high occupancy was observed at striatal D2 receptors (average putamen, 87%; caudate, 93%; and ventral striatum, 91%), lower occupancy at 5-HT2 receptors (54%–60%), and even lower occupancy at 5-HT1A receptors (16%). D2 occupancy levels were significantly correlated with plasma drug concentrations, and even the lowest dose (10 mg) led to 85% D2 occupancy. Extrapyramidal side effects were seen only in two of the four participants with occupancies exceeding 90%. CONCLUSIONS: Aripiprazole exhibits a unique occupancy profile as compared with other conventional and atypical antipsychotics. The threshold for response appears to be higher than 60%, extrapyramidal side effects appear to be uncommon even at occupancies that exceed the conventional extrapyramidal side effects threshold of 80%, and 5-HT2 occupancy is lower than D2 occupancy. Implications for aripiprazole’s mechanism of action are discussed.


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Am J Psychiatry 2007 164: A36. [Full Text] [PDF]



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