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代谢型谷氨酸受体2/3激动剂LY379268对苯环利定致敏大鼠运动活动的影响。

Effects of the mGlu2/3 receptor agonist LY379268 on motor activity in phencyclidine-sensitized rats.

作者信息

Clark Matthew, Johnson Bryan G, Wright Rebecca A, Monn James A, Schoepp Darryle D

机构信息

Neuroscience Research Division, Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Mail Drop 0510, Indianapolis, IN 46285, USA.

出版信息

Pharmacol Biochem Behav. 2002 Sep;73(2):339-46. doi: 10.1016/s0091-3057(02)00848-1.

Abstract

Previous work has shown that mGlu2/3 receptor agonists such as LY379268 inhibit motor responses to acutely administered phencyclidine (PCP) in rats. However, it has not been determined whether mGlu2/3 receptor agonists will reverse the enhanced effects of repeatedly administered PCP (so called PCP sensitization). In these studies, rats were administered daily PCP and monitored for the number of ambulations, fine movements, time at rest and rears using an automated activity system. At Day 10, when compared the first (Day 1) response, PCP-treated animals showed enhanced responses to all measures tested. Augmentations of these PCP-induced behaviors generally peaked between the third and tenth day after PCP administration had begun. Acute administration of LY379268 effectively suppressed PCP-evoked motor behaviors in rats sensitized to PCP. However, daily administrations of LY379268 (for 9 days), along with PCP, did not prevent the expression of the enhanced PCP response on Day 10. Thus, LY379268 administration can suppress PCP responses after either acute or chronic exposure to PCP. However, the underlying plasticity that leads to PCP sensitization was not affected by this treatment.

摘要

先前的研究表明,代谢型谷氨酸受体2/3(mGlu2/3)激动剂,如LY379268,可抑制大鼠对急性给予苯环利定(PCP)的运动反应。然而,mGlu2/3受体激动剂是否会逆转反复给予PCP所产生的增强效应(即所谓的PCP致敏),目前尚未确定。在这些研究中,大鼠每天接受PCP处理,并使用自动活动系统监测其行走、精细运动、静止时间和竖尾次数。在第10天,与首次(第1天)反应相比,接受PCP处理的动物对所有测试指标的反应均增强。这些由PCP诱导的行为增强通常在开始给予PCP后的第3天至第10天达到峰值。急性给予LY379268可有效抑制对PCP致敏的大鼠中PCP诱发的运动行为。然而,每天给予LY379268(持续9天)并同时给予PCP,并未阻止在第10天出现增强的PCP反应。因此,给予LY379268可在急性或慢性暴露于PCP后抑制PCP反应。然而,导致PCP致敏的潜在可塑性并未受到这种处理的影响。

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