Kim Jeong Hoon, Vezina Paul
Department of Psychiatry, The University of Chicago, 5841 S. Maryland Avenue, MC 3077, Chicago, IL 60637, USA.
Pharmacol Biochem Behav. 2002 Sep;73(2):333-7. doi: 10.1016/s0091-3057(02)00827-4.
The present experiments assessed the effect of the Group II-specific metabotropic glutamate receptor (mGluR) agonist, LY379268, on the expression of the locomotor sensitization observed following repeated exposure to amphetamine (AMPH). Rats in different groups were administered five injections of AMPH (1 mg/kg ip), one injection every 2-3 days. Two weeks after the last injection, rats were challenged with either AMPH (1 mg/kg ip) or AMPH coinjected with LY379268 (1 mg/kg ip). As expected, AMPH produced levels of locomotion that increased progressively from the first to the fifth injection. This locomotor sensitization was still evident 2 weeks later in rats challenged with AMPH. Rats challenged on this test with AMPH+LY379268, however, showed levels of locomotion similar to those observed following the first AMPH injection. These results indicate that Group II mGluRs can play an important role in the expression of locomotor sensitization by AMPH. The ability of Group II mGluR activation to block the expression of sensitization indicates that it can be targeted as a possible molecular candidate for the development of therapeutic drugs directed at drugs of abuse.
本实验评估了II型代谢型谷氨酸受体(mGluR)激动剂LY379268对反复给予苯丙胺(AMPH)后观察到的运动敏化表达的影响。不同组的大鼠接受五次AMPH注射(1mg/kg,腹腔注射),每2 - 3天注射一次。最后一次注射两周后,大鼠分别接受AMPH(1mg/kg,腹腔注射)或与LY379268(1mg/kg,腹腔注射)共同注射的AMPH的激发试验。正如预期的那样,AMPH引起的运动水平从第一次注射到第五次注射逐渐增加。在接受AMPH激发试验的大鼠中,这种运动敏化在2周后仍然明显。然而,在该试验中接受AMPH + LY379268激发的大鼠表现出的运动水平与第一次AMPH注射后观察到的相似。这些结果表明,II型mGluR在AMPH引起的运动敏化表达中可能起重要作用。II型mGluR激活阻断敏化表达的能力表明,它可能是开发针对滥用药物的治疗药物的一个潜在分子靶点。