Tyrosine transport was examined in cultured skin fibroblasts from pati
ents with schizophrenia (DSM-III-R) and normal subjects. The transport
capacity (V-max) was lower in the patients. The results confirm previ
ous findings of decreased tyrosine transport in schizophrenia. In cell
s incubated with psychotropic drugs at different concentrations, tyros
ine transport was not differentially influenced across patients and no
rmal subjects. Dopaminergic and beta-adrenergic receptor mechanisms di
d not seem to influence tyrosine uptake. There seems to be a primary d
isturbance of tyrosine transport in schizophrenia which indicates a ge
neralized cell membrane dysfunction.