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氟哌啶醇、舒必利和 SCH 23390 对小鼠被动回避学习的影响。

Effects of haloperidol, sulpiride and SCH 23390 on passive avoidance learning in mice.

作者信息

Ichihara K, Nabeshima T, Kameyama T

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.

出版信息

Eur J Pharmacol. 1988 Jul 14;151(3):435-42. doi: 10.1016/0014-2999(88)90540-7.

Abstract

The main purpose of the present study was to examine the effect of dopamine blockers on memory processes by means of a one-trial passive avoidance (PA) task with ddY mice. Haloperidol (0.025-0.4 mg/kg i.p.) did not affect the PA response when it was given before the training or retention test. Sulpiride (10-80 mg/kg i.p.) had different effects, depending on the doses employed: A lower dose (20 mg/kg) of sulpiride, which is thought to block presynaptic receptors, impaired the PA response but higher doses (40 and 80 mg/kg i.p.) did not affect it when sulpiride was given before the training or retention test. SCH 23390 (0.025-0.1 mg/kg i.p.) impaired the PA response only when it was given before the training. These results suggest that blocking of postsynaptic D-2 receptors does not impair memory processes but blocking of presynaptic D-2 receptors impairs both acquisition and retrieval stages of memory processes following an increase in dopamine release. The involvement of D-1 receptors in memory processes involved in the PA response may be essentially different from that of D-2 receptors, since the blocking of D1 receptors impaired only memory acquisition.

摘要

本研究的主要目的是通过对ddY小鼠进行单次被动回避(PA)任务,来检测多巴胺受体阻滞剂对记忆过程的影响。当在训练或记忆保持测试前腹腔注射氟哌啶醇(0.025 - 0.4毫克/千克)时,对PA反应没有影响。舒必利(10 - 80毫克/千克腹腔注射)根据所用剂量产生不同影响:较低剂量(20毫克/千克)的舒必利被认为可阻断突触前受体,会损害PA反应,但在训练或记忆保持测试前腹腔注射较高剂量(40和80毫克/千克)时则不会产生影响。SCH 23390(0.025 - 0.1毫克/千克腹腔注射)仅在训练前给药时会损害PA反应。这些结果表明,阻断突触后D - 2受体不会损害记忆过程,但在多巴胺释放增加后,阻断突触前D - 2受体则会损害记忆过程的获取和检索阶段。PA反应所涉及的记忆过程中,D - 1受体的作用可能与D - 2受体的作用本质上不同,因为阻断D1受体仅损害记忆获取。

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