Schizophrenia is believed to involve altered activation of dopamine re
ceptors, and support for this hypothesis comes from the antipsychotic
effect of antagonists of the dopamine D2 receptor (D2R)(1). D2R is exp
ressed most highly in the striatum, but most of the recent positron em
ission tomography (PET) studies have failed to show any change in D2R
densities in the striatum of schizophrenics(2-5), raising the possibil
ity that other receptors may also be involved. In particular, the dopa
mine D1 receptor (D1R), which is highly expressed in the prefrontal co
rtex(6), has been implicated in the control of working memory(7,8), an
d working memory dysfunction is a prominent feature of schizophrenia(9
). We have therefore used PET to examine the distribution of D1R and D
2R in brains of drug-naive or drug-free schizophrenic patients. Althou
gh no differences were observed in the striatum relative to control su
bjects, binding of radioligand to D1R was reduced in the prefrontal co
rtex of schizophrenics. This reduction was related to the severity of
the negative symptoms (for instance, emotional withdrawal) and to poor
performance in the Wisconsin Card Sorting Test(10). We propose that d
ysfunction of D1R signalling in the prefrontal cortex may contribute t
o the negative symptoms and cognitive deficits seen in schizophrenia.