The effects of risperidone on the acquisition of schedule-induced poly
dipsia in rats were investigated in a chronic dose regime followed by
seven days of withdrawal. Risperidone dose-dependently suppressed wate
r intake and number of panel pushes. Drinking efficiency and free wate
r intake in home cages were unchanged. By comparing the effects of ris
peridone in the present paper with the effects of different neurolepti
cs in the same procedure from an earlier study, it appears that the ef
fect of risperidone is intermediary to that of the 'typical' and 'atyp
ical' neuroleptics. It may be concluded that risperidone acts as an at
ypical neuroleptic compound; however, increasing the dose only two-fol
d will cause EPS.