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大麻素CB1受体拮抗剂SR141716A可减轻由Δ9-四氢大麻酚或花生四烯酸乙醇胺引起的记忆损害。

The cannabinoid CB1 receptor antagonist SR141716A attenuates the memory impairment produced by delta9-tetrahydrocannabinol or anandamide.

作者信息

Mallet P E, Beninger R J

机构信息

Department of Psychology, Queen's University, Kingston, Ontario, Canada.

出版信息

Psychopharmacology (Berl). 1998 Nov;140(1):11-9. doi: 10.1007/s002130050733.

DOI:10.1007/s002130050733
PMID:9862397
Abstract

The administration of delta9-tetrahydrocannabinol (THC), the principle psychoactive ingredient in marijuana, or the endogenous cannabinoid anandamide, has been shown to impair recent memory. The purpose of the present investigation was to determine if the cannabinoid CB1 receptor antagonist SR141716A could attenuate THC- or anandamide-induced memory impairment, and to assess the effects on memory of SR141716A alone. Memory was assessed in rats well-trained in a two-component instrumental discrimination task, consisting of a conditional discrimination, and a non-match-to-position to assess recent or working memory. SR141716A (0.0-2.0 mg/kg) had no effect on either the conditional discrimination or the non-match-to-position. However, SR141716A (0.0-2.0 mg/kg) attenuated the memory impairment produced by THC (2.0 or 4.0 mg/kg) as indexed by an enhancement of performance in the non-match-to-position. When administered to rats pretreated with anandamide (2.0 mg/kg), SR141716A (0.0-2.5 mg/kg) impaired performance in the conditional discrimination at the highest dose. This was interpreted as a deficit in some capacity unrelated to memory (e.g., motor impairment). However, lower doses of SR141716A (0.1 and 0.5 mg/kg) attenuated the anandamide-induced impairment of performance in the non-match-to-position without affecting the conditional discrimination. This is the first report that the memory impairment produced by anandamide can be attenuated by a cannabinoid antagonist; results suggest that anandamide-induced memory disruption is mediated by CB receptors.

摘要

δ9-四氢大麻酚(THC)是大麻中的主要精神活性成分,内源性大麻素花生四烯酸乙醇胺的给药已被证明会损害近期记忆。本研究的目的是确定大麻素CB1受体拮抗剂SR141716A是否能减轻THC或花生四烯酸乙醇胺诱导的记忆损害,并评估单独使用SR141716A对记忆的影响。在经过两组分工具性辨别任务良好训练的大鼠中评估记忆,该任务包括条件辨别和位置非匹配以评估近期或工作记忆。SR141716A(0.0 - 2.0毫克/千克)对条件辨别或位置非匹配均无影响。然而,SR141716A(0.0 - 2.0毫克/千克)减轻了THC(2.0或4.0毫克/千克)产生的记忆损害,这通过位置非匹配中的表现增强来衡量。当给予用花生四烯酸乙醇胺(2.0毫克/千克)预处理的大鼠时,SR141716A(0.0 - 2.5毫克/千克)在最高剂量下损害了条件辨别的表现。这被解释为与记忆无关的某种能力缺陷(例如,运动障碍)。然而,较低剂量的SR141716A(0.1和0.5毫克/千克)减轻了花生四烯酸乙醇胺诱导的位置非匹配表现损害,而不影响条件辨别。这是第一份关于大麻素拮抗剂可减轻花生四烯酸乙醇胺产生的记忆损害的报告;结果表明花生四烯酸乙醇胺诱导的记忆破坏是由CB受体介导的。

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