bupropion-induce d climbing throu gh d -1 and d-2 dopamine receptor activation

نویسندگان

mohammad-reza zarrindast from the department of pharmacology, faculty of medicine, tehran university of medical sciences, tehran, islamic republic of iran.

yadollah khalenabi

mohammad hossein pourgholami

چکیده

intraperitoneal (ip) injection of bupropion (3,6, amine (4,16 mg kg•&apos;) 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.

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BUPROPION-INDUCE D CLIMBING THROU GH D -1 AND D-2 DOPAMINE RECEPTOR ACTIVATION

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-ad...

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عنوان ژورنال:
medical journal of islamic republic of iran

جلد ۶، شماره ۴، صفحات ۲۸۵-۲۸۹

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