J. Arnt et T. Skarsfeldt, DO NOVEL ANTIPSYCHOTICS HAVE SIMILAR PHARMACOLOGICAL CHARACTERISTICS - A REVIEW OF THE EVIDENCE, Neuropsychopharmacology, 18(2), 1998, pp. 63-101
The pharmacological properties of the novel antipsychotic drugs (APDs)
risperidone, sertindole, olanzapine, quetiapine, ziprasidone, remoxip
ride, and amperozide are reviewed and compared with haloperidol and cl
ozapine. Focus is made on their receptor profiles, their effects in an
imal models used for evaluation of antipsychotic activity, and extrapy
ramidal side effects (EPS). In addition, the contrasting actions of th
ese compounds on animal models of cognition, anxiety, and depression a
re briefly reviewed. The available evidence indicates that novel APDs
and clozapine can be differentiated from haloperidol, particularly in
models of EPS and cognitive side effects. However, among the group of
novel APDs there are many individual differences in models reflecting
limbic versus striatal inhibition of dopamine function: clozapine and
sertindole show the largest limbic selectivity, following by quetiapin
e, ziprasidone, olanzapine and remoxipride, whereas risperidone in man
y respects hits a profile that resembles haloperidol. To date, the res
ults of clinical studies have confirmed the predictions of lower incid
ence or absence of EPS after administration of novel APDs in doses whi
ch demonstrate antipsychotic efficacy. (C) 1998 American College of Ne
uropsychopharmacology. Published by Elsevier Science Inc.