Terranova J P, Storme J J, Lafon N, Péŕio A, Rinaldi-Carmona M, Le Fur G, Soubrié P
Sanofi Recherche, Montpellier, France.
Psychopharmacology (Berl). 1996 Jul;126(2):165-72. doi: 10.1007/BF02246352.
Social short-term memory in rodents is based on the recognition of a juvenile by an adult conspecific when the juvenile is presented on two successive occasions. Cannabimimetics are claimed to induce memory deficits in both humans and animals. In the brain, they mainly bind to CB1 receptors for which anandamide is a purported endogenous ligand. SR 141716, a specific antagonist of CB1 receptors, dose-dependently reverses biochemical and pharmacological effects of cannabimimetics. More particularly, it antagonizes the inhibition of hippocampal long-term potentiation induced by WIN 55,212-2 and anandamide, and it increases arousal when given alone. The present experiments study the ability of SR 141716 (from 0.03 to 3 mg/kg SC) to facilitate short-term olfactory memory in the social recognition test in rodents. SR 141716 improved social recognition in a long intertrial paradigm with a threshold dose of 0.1 mg/kg SC. At 1 mg/kg, it antagonized the memory disturbance elicited by retroactive inhibition. Scopolamine (0.06 mg/kg IP) partially reversed its memory-enhancing effect. Moreover, SR 141716 reduced memory deficit in aged rats (0.03-0.1 mg/kg) and mice (0.3-1 mg/kg). As SR 141716 is not known to exhibit any pharmacological activity which is not mediated by CB1 receptors, the results strongly support the concept that blockade of CB1 receptors plays an important role in consolidation of short-term memory in rodents and suggest there may be a role for an endogenous cannabinoid agonist tone (anandaminergic) in forgetting.
啮齿动物的社交短期记忆基于成年同种个体在连续两次遇到幼崽时对其的识别。大麻模拟物据称会导致人类和动物出现记忆缺陷。在大脑中,它们主要与CB1受体结合,而花生四烯乙醇胺被认为是该受体的内源性配体。CB1受体的特异性拮抗剂SR 141716能剂量依赖性地逆转大麻模拟物的生化和药理作用。更具体地说,它能拮抗WIN 55,212-2和花生四烯乙醇胺对海马体长期增强作用的抑制,并且单独给药时能提高觉醒水平。本实验研究了SR 141716(皮下注射剂量为0.03至3毫克/千克)在啮齿动物社交识别测试中促进短期嗅觉记忆的能力。在长间隔试验范式中,SR 141716能改善社交识别,阈值剂量为皮下注射0.1毫克/千克。在1毫克/千克时,它能拮抗由逆行性抑制引起的记忆障碍。东莨菪碱(腹腔注射0.06毫克/千克)能部分逆转其记忆增强作用。此外,SR 141716能减轻老年大鼠(0.03 - 0.1毫克/千克)和小鼠(0.3 - 1毫克/千克)的记忆缺陷。由于已知SR 141716不表现出任何不由CB1受体介导的药理活性,这些结果有力地支持了这样一种观点,即CB1受体的阻断在啮齿动物短期记忆巩固中起重要作用,并表明内源性大麻素激动剂张力(花生四烯乙醇胺能)在遗忘过程中可能起作用。