Many CNS pathologies, including Parkinson's, Alzheimer's and Huntingto
n's diseases, as well as AIDS dementia complex, involve some degree of
movement dysfunction. Reaction time (RT) performance has been shown t
o be a sensitive measure of motor function for these disorders. Useful
models of RT performance exist in a variety of species, but few are p
erformed in the same manner as with humans. To facilitate species comp
arisons, the present RT task was developed from a human RT task. Dopam
inergic drugs were then used to characterize the sensitivity of the mo
del to CNS changes and to investigate their effects on RT performance
in intact rhesus monkeys. With cumulative dosing, the selective dopami
ne receptor antagonists (D-1) SCH 39166 and (D-2) raclopride produced
dose-dependent slowing of RT performance. Results following bolus admi
nistration of these drugs were consistent with the cumulative dosing p
rocedure, although of smaller magnitude and higher variability. Amphet
amine had no significant effect on group RT performance with either do
sing scheme, but RT performance in individual monkeys was either speed
ed or slowed by d-amphetamine. The present results suggest that blocka
de of either D-1-like or D-2-like dopamine receptors can slow RT perfo
rmance in rhesus monkeys and that this paradigm may be useful to study
movement dysfunction in non-human primates.