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甲基麦角新碱可阻断喹哌嗪对大鼠的睡眠抑制作用。

Methysergide blocks the sleep suppressant action of quipazine in rats.

作者信息

Fornal C, Radulovacki M

出版信息

Psychopharmacology (Berl). 1982;76(3):255-9. doi: 10.1007/BF00432556.

Abstract

The aim of the present study was to examine the effect of methysergide, a 5-hydroxytryptamine (5-HT) receptor antagonist, on the sleep suppression produced by the 5-HT receptor agonist, quipazine. Treatment with methysergide maleate (5 mg/kg, IP) 15 min before the administration of quipazine blocked quipazine-induced suppression of flow-wave sleep (SWS), but failed to prevent the decrease in rapid-eye-movement sleep (REMS) produced by quipazine. Treatment with methysergide also prevented the head-shaking behavior induced by quipazine, a phenomenon associated with increased activity of the central serotonergic system. Furthermore, it was shown that administration of methysergide alone (1 or 5 mg/kg, IP) had little effect on sleep or head-shaking behavior. The present data provide pharmacological evidence that the suppression of SWS but not REMS by quipazine may be a result of stimulation of 5-HT receptors.

摘要

本研究的目的是检验5-羟色胺(5-HT)受体拮抗剂甲基麦角新碱对5-HT受体激动剂喹哌嗪所产生的睡眠抑制作用的影响。在给予喹哌嗪前15分钟腹腔注射马来酸甲基麦角新碱(5毫克/千克)可阻断喹哌嗪诱导的慢波睡眠(SWS)抑制,但未能防止喹哌嗪所导致的快速眼动睡眠(REMS)减少。甲基麦角新碱治疗还可防止喹哌嗪诱导的摇头行为,这一现象与中枢5-羟色胺能系统活性增加有关。此外,研究表明单独给予甲基麦角新碱(1或5毫克/千克,腹腔注射)对睡眠或摇头行为影响很小。目前的数据提供了药理学证据,表明喹哌嗪对SWS而非REMS的抑制可能是刺激5-HT受体的结果。

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