Induction of turning by direct intrastriatal injection of dopaminomimetic drugs in mice: pharmacological analysis of a simple screening model

• Published in: Life sciences (1973) Vol. 39; no. 23; p. 2199
• Main Authors: Worms, P, Gueudet, C, Biziere, K
• Format: Journal Article
• Language: English
• Published: Netherlands 08.12.1986
• Subjects: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Animals; Apomorphine - pharmacology; Benzazepines - pharmacology; Bromocriptine - pharmacology; Dextroamphetamine - pharmacology; Dopamine - pharmacology; Female; Haloperidol - pharmacology; Mice; Nomifensine - pharmacology; Posture - drug effects; Pyridazines - pharmacology; Stereotyped Behavior - drug effects; Sulpiride - pharmacology; Time Factors
• ISSN: 0024-3205
• DOI: 10.1016/0024-3205(86)90397-8

A new simple model designed for the screening of dopaminomimetic drugs in mice is presented. When injected directly into the right striatum of conscious mice, the dopamine (DA) receptor agonists apomorphine, SKF 38393 and bromocryptine, the indirect DAmimetic drugs (+)-amphetamine and nomifensine, the atypical DAergic antidepressant drug minaprine, induced contralateral rotations. Rotations induced by DA mimetics were antagonized by i.p. injected haloperidol. A pretreatment with the D1 antagonist SCH 23390 (s.c.) antagonized the turning induced by apomorphine or by the D1 agonist SKF 38393, and, to a lesser extent, that induced by the D2 agonist bromocryptine. In contrast, the D2 antagonist (-)-sulpiride (i.p.) blocked the effects of the 3 agonists to the same extent. A pretreatment with alpha-methylparatyrosine (i.p.) antagonized rotations induced by bromocryptine, (+)-amphetamine and minaprine, but not those induced by nomifensine or apomorphine. The results suggest that this model could represent a useful screening tool for the search of new DAmimetic drugs, and for the assessment of DA receptor blockade.