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在注射吗啡的大鼠中,SKF 38393将多巴胺D2受体介导的向前运动转变为向后行走。

In morphinised rats SKF 38393 converts dopamine D2 receptor-mediated forward locomotion into backward walking.

作者信息

Axon D I, Fletcher G H, Starr M S

出版信息

Pharmacol Biochem Behav. 1987 Jan;26(1):45-7. doi: 10.1016/0091-3057(87)90531-4.

Abstract

The behavioural responses to RU 24213 (D2 agonist) and SKF 38393 (D1 agonist) were studied in the morphine cataleptic rat. D2 stimulation evoked slow forward walking coupled with head-down sniffing that was blocked both by SCH 23390 (D1 antagonist) and metoclopramide (D2 antagonist). D1 stimulation was without effect by itself, but when administered together with RU 24213 it reversed the direction of walking and initiated licking and chewing. Backward walking was attenuated by metoclopramide and restored to forward locomotion by SCH 23390. These data further show that D1 receptors exert an important modulatory influence on motor behaviours mediated by the D2 site.

摘要

在吗啡诱导僵住的大鼠中研究了对RU 24213(D2激动剂)和SKF 38393(D1激动剂)的行为反应。D2刺激引发缓慢向前行走并伴有低头嗅闻,这两种反应均被SCH 23390(D1拮抗剂)和甲氧氯普胺(D2拮抗剂)阻断。D1刺激本身无作用,但与RU 24213一起给药时,它会使行走方向反转并引发舔舐和咀嚼。甲氧氯普胺减弱了向后行走,而SCH 23390使其恢复为向前运动。这些数据进一步表明,D1受体对由D2位点介导的运动行为发挥重要的调节作用。

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