Worms P, Gueudet C, Biziere K
Life Sci. 1986 Dec 8;39(23):2199-208. 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.
本文介绍了一种为筛选小鼠多巴胺模拟药物而设计的新型简单模型。当直接注射到清醒小鼠的右侧纹状体时,多巴胺(DA)受体激动剂阿扑吗啡、SKF 38393和溴隐亭、间接多巴胺模拟药物(+)-苯丙胺和诺米芬辛、非典型多巴胺能抗抑郁药物米那普明可诱导对侧旋转。多巴胺模拟物诱导的旋转可被腹腔注射氟哌啶醇拮抗。用D1拮抗剂SCH 23390(皮下注射)预处理可拮抗阿扑吗啡或D1激动剂SKF 38393诱导的旋转,对D2激动剂溴隐亭诱导的旋转拮抗作用较小。相反,D2拮抗剂(-)-舒必利(腹腔注射)在相同程度上阻断了这3种激动剂的作用。用α-甲基对酪氨酸(腹腔注射)预处理可拮抗溴隐亭、(+)-苯丙胺和米那普明诱导的旋转,但不能拮抗诺米芬辛或阿扑吗啡诱导的旋转。结果表明,该模型可能是寻找新型多巴胺模拟药物以及评估多巴胺受体阻断作用的有用筛选工具。