Department of Psychology, University of Connecticut, Storrs, CT 06269-1020, USA.
Pharmacol Biochem Behav. 2010 Jun;95(4):479-84. doi: 10.1016/j.pbb.2010.03.011. Epub 2010 Mar 27.
The effects of CB1 antagonist/inverse agonists on the acquisition and consolidation of conditioned fear remain uncertain. Recent studies suggest that the CB1 antagonist/inverse agonist AM251 affects acquisition or consolidation of both contextual and discretely cued fear memories. AM251 is frequently referred to as a CB1 antagonist; however in vitro signal transduction assays indicate that this drug also elicits inverse agonist activity at CB1 receptors. The present studies were undertaken to compare the effects of AM251 on conditioned fear with those produced by AM4113, a novel CB1 antagonist with minimal inverse agonist activity. All drugs were administered prior to conditioning. In retention tests conducted two weeks after conditioning, both AM251 (4.0 mg/kg) and AM4113 (6.0 mg/kg)-treated animals exhibited reduced freezing during a conditioned tone cue played within a novel context. In contextual fear retention tests, animals previously treated with 4.0 or 8.0 mg/kg AM251 exhibited enhanced freezing. By contrast, no dose of AM4113 had any significant effect on contextual fear memory, which is consistent with the lower signal transduction activity of AM4113 at CB1 receptors compared to AM251. These results suggest that CB1 neutral antagonists may be less likely than CB1 inverse agonists to facilitate the acquisition or consolidation of contextual fear that may contribute to some clinical disorders.
CB1 拮抗剂/反向激动剂对条件性恐惧的获得和巩固的影响仍不确定。最近的研究表明,CB1 拮抗剂/反向激动剂 AM251 影响情境和离散线索恐惧记忆的获得或巩固。AM251 通常被称为 CB1 拮抗剂;然而,体外信号转导测定表明,该药物还在 CB1 受体上引发反向激动剂活性。本研究旨在比较 AM251 对条件性恐惧的影响与 AM4113 的影响,AM4113 是一种新型 CB1 拮抗剂,具有最小的反向激动剂活性。所有药物均在条件作用前给予。在条件作用后两周进行的保留测试中,AM251(4.0mg/kg)和 AM4113(6.0mg/kg)处理的动物在新环境中播放条件性音调提示时,表现出明显的冻结减少。在情境恐惧保留测试中,先前用 4.0 或 8.0mg/kg AM251 处理的动物表现出增强的冻结。相比之下,AM4113 的任何剂量都没有对情境恐惧记忆产生显著影响,这与 AM4113 在 CB1 受体上的信号转导活性低于 AM251 一致。这些结果表明,CB1 中性拮抗剂可能不如 CB1 反向激动剂更容易促进情境恐惧的获得或巩固,这可能导致某些临床障碍。