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吗啡通过间接多巴胺能机制刺激运动活性:可能涉及D-1和D-2受体。

Morphine stimulates locomotor activity by an indirect dopaminergic mechanism: possible D-1 and D-2 receptor involvement.

作者信息

Zarrindast M R, Zarghi A

机构信息

Department of Pharmacology, Medical Faculty, University of Tehran, Iran.

出版信息

Gen Pharmacol. 1992 Nov;23(6):1221-5. doi: 10.1016/0306-3623(92)90315-b.

DOI:10.1016/0306-3623(92)90315-b
PMID:1362552
Abstract
  1. The effect of morphine on locomotor activity in mice and the mechanism involved were evaluated. 2. Subcutaneous (s.c.) injection of different doses of morphine (10, 20 and 40 mg kg-1) into mice induced a dose-dependent locomotor activity. 3. The response to morphine was decreased in animals pretreated by the D-1 antagonist SCH 23390, the D-2 antagonist sulpiride or the opiate receptor antagonist naloxone, but not by atropine, phenoxybenzamine, propranolol and methergoline. 4. The inhibitory effects of SCH 23390, sulpiride or naloxone were dose-dependent. 5. Pretreatment with reserpine prevented the effect of morphine. SKF 38393 (D-1 agonist) or quinpirole (D-2 agonist) also induced locomotor activity in mice. Also this effect was decreased by reserpine pretreatment. 6. Combination of SKF 38393 with quinpirole but not of morphine with SKF 38393 or quinpirole induced a high degree of locomotor activity in intact and reserpinized animals. 7. It is concluded that locomotor activity induced by morphine is mediated by opiate receptor through an indirect dopaminergic mechanism.
摘要
  1. 评估了吗啡对小鼠运动活性的影响及其相关机制。2. 给小鼠皮下注射不同剂量的吗啡(10、20和40毫克/千克)可诱导剂量依赖性的运动活性。3. 用D-1拮抗剂SCH 23390、D-2拮抗剂舒必利或阿片受体拮抗剂纳洛酮预处理的动物对吗啡的反应降低,但用阿托品、酚苄明、普萘洛尔和麦角新碱预处理则无此效果。4. SCH 23390、舒必利或纳洛酮的抑制作用呈剂量依赖性。5. 利血平预处理可阻断吗啡的作用。SKF 38393(D-1激动剂)或喹吡罗(D-2激动剂)也可诱导小鼠运动活性。利血平预处理也可降低这种作用。6. SKF 38393与喹吡罗联合使用可诱导完整和利血平化动物产生高度的运动活性,但吗啡与SKF 38393或喹吡罗联合使用则无此效果。7. 得出结论:吗啡诱导的运动活性是通过阿片受体经间接多巴胺能机制介导的。

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