1. Both L-dopa and low doses of apomorphine potentiated withdrawal sym
ptoms such as jumping, ''wet dog'' shakes and burrows. L-dopa reduced
hypothermia and potentiated body weight loss, whereas apomorphine prod
uced opposite effects. 2. Higher doses of apomorphine attenuated jumpi
ng and burrows but had no effect on ''wet dog'' shakes. On the other h
and, and with the exception of sulpiride, all other dopamine (DA) anta
gonists produced effects opposite those of the agonists with regard to
jumping, ''wet dog'' shakes and burrows. 3. In addition, DA antagonis
ts reduced hypothermia and body weight loss. The effects of DA agonist
s and antagonists were investigated in mice injected with 6-hydroxydop
amine (6-OHDA) intracerebrally to examine whether DA mediated effects
are somehow linked to noradrenergic pathways. 4. Mice pretreated with
6-OHDA developed a higher degree of naloxone induced withdrawal jump i
ng than did untreated mice. 6-OHDA reversed the effects of apomorphine
on ''wet dog'' shakes and burrows while abolishing those of L-dopa on
all withdrawal symptoms, the only exception being jumping, which rema
ined unchanged. 5. 6-OHDA also reversed the effects of sulpiride on al
l withdrawal symptoms while reversing the effects of pimozide on jumpi
ng, and it abolished its effect on hypothermia. 6. These findings prov
ide evidence suggesting that the effects of DA agonists and antagonist
s are dependent at least partly on intact noradrenergic pathways. (C)
1998 Elsevier Science Inc.