Journal
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
Volume 31, Issue 2, Pages 348-356Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pnpbp.2006.09.007
Keywords
aripiprazole; dopamine; in vitro binding assay; partial agonist; schizophrenia
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Clinical evidence suggests that dopamine D-2 receptor partial agonists must have a sufficiently low intrinsic activity to be effective as antipsychotics. Here, we used dopamine D2 receptor signaling assays to compare the in vitro functional characteristics of the antipsychotic aripiprazole with other dopamine D2 receptor partial agonists (7-{3-[4-(2,3-dimethylphenyl)-piperazinyl]propoxy}-2(IH)-quinolinone [OPC-4392], (-)-3-(3-hydroxy-phenyl)-N-n-propylpiperidiiie [(-)3-PPP] and (+)terguride) and dopamine D2 receptor antagonists. Aripiprazole and OPC-4392 were inactive in a guanosine-5'-O-(3-[S-35]thio)-triphosphate ([S-35]GTP-gamma S) binding assay using Chinese Hamster Ovary (CHO) cell membranes expressing cloned human dopamine D-2Long (hD(2L)) receptors, whereas (-)3-PPP and (+)terguride displayed low intrinsic activity. Aripiprazole also had no effect on [S-35]GTP-gamma S binding to CHO-hD(2L) cells, while OPC-4392, (-)3-PPP and (+)terguride were partial agonists. In contrast, aripiprazole, OPC-4392, (-)3-PPP, and (+)terguride were inactive in a [S-35]GTP-gamma S binding assay using,rat striatal membranes. However, at a more downstream level of CHO-hD(2L) cell signalling, these drugs all behaved as dopamine hD2L receptor partial agonists, with aripiprazole displaying an intrinsic activity 2 to 3-fold lower (inhibition of forskolin-induced adenosine 3',5'-cyclic monophosphate accumulation) and almost half as high (enhancement of adenosine triphospliate-stimulated [H-3]arachidonic acid release) as OPC-4392, (-)3-PPP and (+)terguride. Dopamine activity was blocked in each case by (-)raclopride, which was inactive on its own in every assay, as were the antipsychotics haloperidol, olanzapine, ziprasidone and clozapine. Together, these data, whilst preclinical in nature, are consistent with clinical evidence suggesting the favorable antipsychotic profile of aripiprazole, compared with the other clinically ineffective partial agonists, is dependent on its low intrinsic activity at dopamine D-2 receptors. This study also highlights the limitations of using [S-35]GTP gamma S binding assays to identify dopamine D-2 receptor partial agonists. (c) 2006 Elsevier Inc. All rights reserved.
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