David H N, Abraini J H
UMR CNRS 6551, Centre CYCERON, Université de Caen Basse-Normandie, Boulevard Henri Becquerel, BP 5229, 14074 Caen cedex, France.
Neuropharmacology. 2003 May;44(6):717-27. doi: 10.1016/s0028-3908(03)00052-2.
Previous investigations have shown that mGlu receptors would be involved in the amphetamine-induced motor response. However, data are somewhat controversial across studies where methodological protocols vary. The aim of the present study was to determine the involvement of mGlu receptors in the NAcc in the locomotor-activating properties of amphetamine in rats well habituated to their experimental environment, a condition known to modulate the motor response to amphetamine. Focal infusion of the group I mGlu receptor antagonist S-4-CPG, which has no effect on basal motor activity, virtually suppressed the locomotor response to amphetamine, while infusion of the group II mGlu receptor antagonist LY 341495 or the group III mGlu receptor agonist AP4, at the minimal dose that produces locomotor activation, reduced it by approximately a half. These effects were blocked by the group I mGlu receptor agonist DHPG, the group II mGlu receptor agonist APDC, and the group III mGlu receptor antagonist MPPG, respectively. These data confirm that mGlu receptors in the NAcc contribute to the psychostimulant motor effect of amphetamine. Results are discussed from the view of recent neuropharmacological studies that have defined the effects of these mGlu receptor ligands on basal motor activity and DA receptor agonists-induced locomotor responses in rats exposed to similar experimental procedures (Eur J Neuroscience 13 (2001) 2157; Neuropharmacology 41 (2001) 454; Eur J Neuroscience 13 (2001) 869). It is suggested that the contribution of mGlu receptors to the amphetamine-induced motor response may result mainly from their functional, either direct or indirect, interactions with D1-like receptors in the NAcc.
先前的研究表明,代谢型谷氨酸受体(mGlu受体)参与苯丙胺诱导的运动反应。然而,由于研究方法不同,各项研究的数据存在一定争议。本研究的目的是确定在对实验环境高度适应的大鼠中,mGlu受体在伏隔核(NAcc)中对苯丙胺运动激活特性的作用,这种条件已知可调节对苯丙胺的运动反应。向NAcc局部注入对基础运动活动无影响的I组mGlu受体拮抗剂S-4-CPG,实际上可抑制对苯丙胺的运动反应,而注入II组mGlu受体拮抗剂LY 341495或III组mGlu受体激动剂AP4(产生运动激活的最小剂量),可使运动反应降低约一半。这些作用分别被I组mGlu受体激动剂DHPG、II组mGlu受体激动剂APDC和III组mGlu受体拮抗剂MPPG阻断。这些数据证实,NAcc中的mGlu受体有助于苯丙胺的精神兴奋运动效应。从最近的神经药理学研究角度对结果进行了讨论,这些研究确定了这些mGlu受体配体对暴露于类似实验程序的大鼠基础运动活动和多巴胺受体激动剂诱导的运动反应的影响(《欧洲神经科学杂志》13卷(2001年)2157页;《神经药理学》41卷(2001年)454页;《欧洲神经科学杂志》13卷(2001年)869页)。提示mGlu受体对苯丙胺诱导的运动反应的作用可能主要源于它们与NAcc中D1样受体直接或间接的功能相互作用。