From the Department of Pharmacology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Islamic Republic of Iran.
Abstract: (4180 Views)
Intraperitoneal (IP) injection of bupropion (3,6,
amine (4,16 mg kg•') induced dose-dependent climbing in mice. The climbing
response induced by both drugs were decreased in animals pretreated either with
the 0-1 antagonist SCH 233<)0 or the 0-2 antagonist sulpiride. The α-adrenoceptor
blocker phenoxybenzamine decreased the climbing induced by both bupropion
and amphetamine, but the β-adrenergic blocker propranolol and the antimuscarinic
agent atropine had no effect. Reserpine pretreatment abolished the climbing
induced by bupropion but not that of amphetamine. However, alpha-methyl-ptyrosine
combined with reserpine treatment reduced the amphetamine-induced
climbing. It is concluded that both bupropion and amphetamine-induced climbing
through release of dopamine and subsequent activation of 0-1/0-2 receptors
however, the mechanisms by which dopamine is released by these drugs may
differ.