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内源性阿片类物质参与胆囊收缩素与脑多巴胺系统相互作用的行为学证据。

Behavioral evidence for the involvement of endogenous opioids in the interaction between cholecystokinin and brain dopamine systems.

作者信息

Király I, Van Ree J M

出版信息

Neurosci Lett. 1987 Mar 9;74(3):343-7. doi: 10.1016/0304-3940(87)90321-1.

Abstract

The hyperactivity induced by injection of the dopamine (DA) agonist apomorphine into the nucleus accumbens of rats was dose dependently inhibited by intra-accumbal pretreatment with cholecystokinin (CCK-8) (ED50, 0.34 ng). Local treatment with the opioid antagonist naloxone antagonized this inhibitory action of CCK-8 (ED50, 18 ng), but did not change the blocking effect of haloperidol on the apomorphine-induced hyperactivity. These data show that endogenous opioids are concerned in certain interactions between CCK-8 and DA systems.

摘要

向大鼠伏隔核注射多巴胺(DA)激动剂阿扑吗啡所诱导的多动,可被伏隔核内预先注射胆囊收缩素(CCK-8)(半数有效量,0.34纳克)剂量依赖性地抑制。用阿片类拮抗剂纳洛酮进行局部处理可拮抗CCK-8的这种抑制作用(半数有效量,18纳克),但不改变氟哌啶醇对阿扑吗啡诱导的多动的阻断作用。这些数据表明,内源性阿片类物质参与了CCK-8与DA系统之间的某些相互作用。

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