多巴胺能受体亚型参与小鼠秸秆尾行为。

M R Zarrindast, A Bayat, B Shafaghi
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引用次数: 11

摘要

1. 阿波啡给药小鼠诱导稻草尾行为呈剂量依赖性。D1拮抗剂SCH 23390和D2拮抗剂舒必利可降低反应。利血平加α -甲基-对酪氨酸(AMPT),引起药物反应的显著增加。2. D1激动剂SKF 38393呈剂量依赖性诱导秸秆尾行为,SCH 23390、舒必利或利血平+ AMPT可降低这种行为。3.当动物服用D2激动剂喹匹罗时,产生了剂量依赖性反应。舒必利和利血平+ AMPT可降低这种效应,但SCH 23390不能。4. 在利血平+ AMPT预处理的动物中,SKF 38393与喹匹罗联合使用产生了显著的秸秆尾行为。5. 由此可见,D1/D2多巴胺受体的同步刺激是小鼠产生秸秆尾行为的必要条件。
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Involvement of dopaminergic receptor subtypes in straub tail behaviour in mice.

1. Administration of apomorphine to mice induced straub tail behaviour dose-dependently. The response was decreased by the D1 antagonist SCH 23390, the D2 antagonist sulpiride. Reserpine plus alpha-methyl-p-tyrosine (AMPT), caused a marked increase in the response of the drug. 2. The D1 agonist SKF 38393 induced the straub tail behaviour in a dose-dependent manner, which was decreased by SCH 23390, sulpiride or reserpine + AMPT. 3. When animals were administered the D2 agonist quinpirole, a dose-dependent response was produced. This effect was decreased by sulpiride and reserpine + AMPT, but not by SCH 23390. 4. In animals pretreated with reserpine + AMPT, the combination of SKF 38393 with quinpirole produced a significant straub tail behaviour. 5. It is concluded that the concurrent D1/D2 dopamine receptor stimulation is necessary to produce straub tail behaviour in mice.

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