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阻断 mGLUR5 受体可改变安非他命诱导的运动活动增强和脑刺激奖励的作用。

Blockade of mGLUR5 receptors differentially alters amphetamine-induced enhancement of locomotor activity and of brain stimulation reward.

机构信息

Hôpital Louis-H. Lafontaine, Montréal, Québec, Canada.

出版信息

J Psychopharmacol. 2011 Mar;25(3):393-401. doi: 10.1177/0269881110367460. Epub 2010 May 24.

Abstract

This study was aimed at determining the role of mGLUR5 glutamate receptors on amphetamine-induced enhancement of locomotion and of brain stimulation reward (BSR). The effect of different doses of the mGLUR5 antagonist, MPEP (0, 1, 3 and 9 mg/kg, i.p.), was assessed on reward induced by electrical stimulation of the lateral hypothalamus, and on the enhancement of reward by amphetamine (1 mg/kg, i.p.) in adult male Long Evans rats. The effect of a single dose of MPEP (0 and 9 mg/kg) on amphetamine-induced increase in locomotor activity was also assessed. Systemic injection of MPEP alone did not alter reward threshold and maximum rate of responding. Amphetamine produced a 25-30% decrease in reward threshold, an effect not altered by the highest dose of MPEP. At this dose, MPEP produced a weak inhibition of spontaneous locomotion and a significant attenuation of the enhanced locomotor activity induced by amphetamine. These findings show that mGLUR5 glutamate receptors are unlikely to constitute important elements of the reward-relevant pathway, and do not intervene in the enhancement effect of amphetamine. They also show, however, that these glutamate receptors play a key role in amphetamine-induced increased locomotor activity, providing additional evidence for a dissociation between the substrates that mediate these two behaviours.

摘要

本研究旨在确定 mGLUR5 谷氨酸受体在安非他命诱导的运动增强和脑刺激奖励(BSR)中的作用。通过评估不同剂量的 mGLUR5 拮抗剂 MPEP(0、1、3 和 9 mg/kg,ip)对侧下丘脑电刺激诱导的奖励以及安非他命(1 mg/kg,ip)增强奖励的影响,评估了成年雄性长耳大鼠。还评估了单次 MPEP(0 和 9 mg/kg)剂量对安非他命诱导的运动活动增加的影响。MPEP 单独全身注射不会改变奖励阈值和最大反应率。安非他命使奖励阈值降低了 25-30%,最高剂量的 MPEP 并未改变这种作用。在此剂量下,MPEP 对自发运动产生微弱抑制,并显著减弱安非他命诱导的运动增强。这些发现表明 mGLUR5 谷氨酸受体不太可能构成奖励相关途径的重要组成部分,也不干预安非他命的增强作用。然而,它们还表明这些谷氨酸受体在安非他命诱导的运动活动增加中起着关键作用,为介导这两种行为的基质之间的分离提供了额外的证据。

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