Aminorex is a cyclic phenylisopropylamine that has been marketed as an
anorectic. Despite obvious pharmacological similarities to the amphet
amines, little is known about its liability for abuse. In the present
study, one group of rhesus monkeys (n = 3) was prepared with intraveno
us catheters and allowed to self-administer either methohexital or sal
ine in daily experimental sessions. When methohexital and saline self-
administration were stable and clearly different, various doses of ami
norex (0.001-0.1 mg/kg/injection) were made available for self-adminis
tration. Aminorex maintained self-administration above that maintained
by saline and slightly lower than that maintained by methohexital in
all monkeys. The discriminative stimulus effects of aminorex were eval
uated in rhesus monkeys trained to discriminate d-amphetamine (n = 3)
or pentobarbital (n = 4) from saline. Aminorex substituted completely
for d-amphetamine as a discriminative stimulus but engendered little o
r no pentobarbital-appropriate responding. Aminorex stimulated locomot
or activity in mice and exacerbated the withdrawal syndrome in rats th
at were dependent upon pentobarbital. These findings indicate that ami
norex is a psychomotor stimulant that would be predicted to have signi
ficant d-amphetamine-like abuse liability in humans.