Many early antipsychotics such as haloperidol, while effective in trea
ting the symptoms of schizophrenia, cause detrimental side effects and
moreover induce nonspecific sedation in many patients. Newer drugs su
ch as remoxipride are as effective as the classical antipsychotics but
induce fewer debilitating side effects. These clinical properties are
reflected to some extent in their preclinical pharmacology, with drug
s such as remoxipride having effects on various preclinical behavioura
l and biochemical models that are quite different to those exerted by
drugs such as haloperidol. This article reports some new behavioural d
ata and discusses the various mechanisms that can underlie the effect
of new atypical antipsychotics.