Several phenyl-benzazepine compounds, putatively selective dopanzine D-1 re
ceptor agonists, have been used to study the effects of dopamine D-1 recept
or stimulation in rodents and nonhuman primates. However, the dopamine rece
ptor selectivities of these compounds have not been established in nonhuman
primates. Accordingly, the relative selectivities of six phenyl-benzazepin
es for dopamine D-1-like and D-2-like receptors were assessed in rhesus mon
key and, for comparison, rat striata. The compounds tested had higher affin
ity for D-1 than D-2 receptors in both species; however, their selectivity
varied by up to three orders of magnitude. GTP (100 mu M) reduced agonist b
inding at the high-affinity state of the dopamine D-1 receptor, but the mag
nitude of the effect of CTP did not reliably predict a compound's efficacy.
Furthermore, a history of cocaine self-administration did not appear to in
fluence dopamine receptor binding characteristics in the rhesus monkeys in
this study. The present results will aid the comparison of dopamine recepto
r binding characteristics and behavioral effects of D-1 dopamine receptor a
gonists. (C) 1998 Elsevier Science B.V. All rights reserved.