多巴胺受体拮抗剂对自由活动大鼠纹状体内灌注甲基苯丙胺诱导的体内多巴胺释放的影响。

Effect of dopamine receptor antagonist on in vivo dopamine release induced by intrastriatal perfusion with methamphetamine in freely moving rats.

作者信息

Watanabe H, Sekihara S, Nomura Y

机构信息

Research Institute for Wakan-Yaku, Toyama Medical and Pharmaceutical University, Japan.

出版信息

Methods Find Exp Clin Pharmacol. 1989 Feb;11(2):81-5.

DOI:
PMID:2709920
Abstract

In order to investigate a regulatory role of dopamine receptors in drug-induced release in the striatum, we determined dopamine and its metabolites in dialysates simultaneously with behavioral observations following intrastriatal perfusion with methamphetamine using the transstriatal dialysis method in freely moving rats. Intrastriatal perfusion with methamphetamine (5, 50, 500 microM) for 40 min produced a marked increase in dopamine release and a slight reduction in 3,4-dihydroxyphenylacetic acid release. No significant changes in spontaneous motor activity were observed after methamphetamine at concentrations up to 500 microM. Methamphetamine-induced dopamine release was not affected by the selective D1-receptor antagonist SCH 23390 (1 microM), but was markedly enhanced by the selective D2-receptor antagonist sulpiride (1 microM), at a concentration that did not change the basal level. Intrastriatal pretreatment with kainic acid (1 micrograms into bilateral striata) slightly affected the dopamine release induced by methamphetamine. These results suggest that methamphetamine-induced dopamine release is regulated by both pre- and postsynaptic D-2 receptors in the striatum in vivo.

摘要

为了研究多巴胺受体在纹状体药物诱导释放中的调节作用,我们采用经纹状体透析法,在自由活动的大鼠纹状体内灌注甲基苯丙胺后,通过行为观察同时测定透析液中的多巴胺及其代谢产物。用甲基苯丙胺(5、50、500微摩尔)在纹状体内灌注40分钟,导致多巴胺释放显著增加,3,4-二羟基苯乙酸释放略有减少。浓度高达500微摩尔的甲基苯丙胺给药后,自发运动活动未观察到显著变化。甲基苯丙胺诱导的多巴胺释放不受选择性D1受体拮抗剂SCH 23390(1微摩尔)的影响,但在不改变基础水平的浓度下,选择性D2受体拮抗剂舒必利(1微摩尔)可显著增强其释放。用 kainic 酸(双侧纹状体各1微克)进行纹状体内预处理对甲基苯丙胺诱导的多巴胺释放有轻微影响。这些结果表明,甲基苯丙胺诱导的多巴胺释放在体内受纹状体中突触前和突触后D2受体的调节。

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