In the present study, we investigated the effects of repeated morphine pre-treatment on impairment of spatial memory acquisition induced by intra dorsal hippocampus (intra-CA1) administration of the non-selective cannabinoid CB1/CB2 receptor agonist, WIN55,212-2 in adult male rats. 2-day version of Morris water maze task has been used for the assessment of spatial memory. On the training day, rats were trained by a single training session of eight trials and 24 h later a probe trial test consist of 60s free swim period without a platform and the visible test was administered. Animals received pre-treatment subcutaneous (s.c.) injections of morphine, once daily for three days followed by five days drug-free treatment before training trials. The results indicated that bilateral pre-training intra-CA1 infusions of WIN55,212-2 (0.25 and 0.5 μg/rat) impaired acquisition of spatial memory on the training and test day. The amnesic effect of WIN55, 212-2 (0.5 μg/rat) was prevented in rats previously injected with morphine (20 mg/kg/day × 3 days, s.c.). Improvement in spatial memory acquisition in morphine-pretreated rats was inhibited by once daily administration of naloxone (1 and 2 mg/kg, s.c.) 15 min prior to injection of morphine for three days. The results suggest that sub-chronic morphine treatment may produced sensitization to cannabinoids, which in turn reversed the impairment of spatial memory acquisition induced by WIN55,212-2 and mu- opioid receptors may play an important role in this effect.

译文

:在本研究中,我们研究了重复吗啡预处理对非选择性大麻素CB1 / CB2受体激动剂WIN55,212-2背侧海马内(CA1内)给药引起的空间记忆获得障碍的影响在成年雄性大鼠中。莫里斯水迷宫任务的2天版本已用于评估空间记忆。在训练当天,通过八次试验的单次训练对大鼠进行了训练,并且在24小时后,探针试验测试包括无平台的60秒钟自由游泳期,并进行了可见测试。在训练试验前,动物每天接受一次皮下(s.c.)皮下注射吗啡治疗,连续三天,然后进行五天的无毒治疗。结果表明,WIN55,212-2(0.25和0.5μg/大鼠)的双训练前CA1内输注在训练和测试当天损害了空间记忆的获取。在事先注射吗啡(20 mg / kg /天×3天,s.c.)的大鼠中,WIN55,212-2(0.5μg/大鼠)的记忆消除得到了预防。在吗啡注射3天前每天15分钟每天一次给予纳洛酮(1和2 mg / kg,皮下注射),抑制了吗啡预处理大鼠的空间记忆获得性改善。结果表明,亚慢性吗啡治疗可能对大麻素产生致敏作用,从而逆转了由WIN55,212-2引起的空间记忆获得障碍,而多阿片受体可能在这种作用中起重要作用。

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