伏隔核中的一氧化氮参与尼古丁对抑制性回避记忆的提取。
Nitric oxide in the nucleus accumbens is involved in retrieval of inhibitory avoidance memory by nicotine.
机构信息
Department of Neuroscience, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, Iran.
出版信息
Pharmacol Biochem Behav. 2012 Mar;101(1):166-73. doi: 10.1016/j.pbb.2011.11.010. Epub 2011 Nov 22.
In the present study, the possible effect of nitric oxide agents injected into the nucleus accumbens (NAc) in the presence or absence of nicotine on morphine state-dependent memory in adult male Wistar rats was investigated. As a model of memory, a step-through type inhibitory avoidance task was used. Post-training injection of morphine (4 and 6mg/kg) dose dependently induced the impairment of memory retention. Administration of morphine (4 and 6mg/kg) before retention induced state-dependent retrieval of the memory acquired under post-training morphine (6mg/kg) influence. Injection of nicotine before retention (0.25 and 0.5mg/kg) alone and nicotine (0.1, 0.25 and 0.5mg/kg) plus an ineffective dose of morphine (2mg/kg) reversed the post-training morphine-induced memory impairment. The amnesia elicited by morphine (6mg/kg) was also prevented by pre-retention intra-NAc administration of a nitric oxide synthase (NOS) inhibitor, l-NAME (0.24μg/rat, intra-NAc). Interestingly, an ineffective dose of nicotine (0.1mg/kg) in combination with low doses of l-NAME (0.06 and 0.12μg/rat, intra-NAc) synergistically improved memory performance impaired by morphine given after training. It is important to note that intra-NAc administration of l-NAME before retention impaired memory retrieval by itself. In contrast, pre-retention administration of l-arginine, a nitric oxide (NO) precursor (0.25 and 0.5μg/rat, intra-NAc), which had no effect alone, prevented the nicotine reversal of morphine effect on memory. The results suggest a possible role for nitric oxide of nucleus accumbens in the improving effect of nicotine on the morphine-induced amnesia and morphine state-dependent memory.
在本研究中,研究了在存在或不存在尼古丁的情况下将一氧化氮(NO)试剂注入伏隔核(NAc)对成年雄性 Wistar 大鼠吗啡状态依赖记忆的可能影响。作为记忆模型,使用了一步式抑制回避任务。训练后注射吗啡(4 和 6mg/kg)剂量依赖性地引起记忆保留受损。在保留前给予吗啡(4 和 6mg/kg)的给药会导致在训练后吗啡(6mg/kg)影响下获得的记忆的状态依赖性检索。单独给予尼古丁(0.25 和 0.5mg/kg)或尼古丁(0.1、0.25 和 0.5mg/kg)加无效剂量的吗啡(2mg/kg)可以逆转训练后吗啡引起的记忆损伤。在保留前给予 NAc 内一氧化氮合酶(NOS)抑制剂 l-NAME(0.24μg/rat)也可以预防吗啡(6mg/kg)引起的遗忘。有趣的是,无效剂量的尼古丁(0.1mg/kg)与低剂量的 l-NAME(0.06 和 0.12μg/rat)联合使用可协同改善训练后给予吗啡引起的记忆障碍。重要的是,保留前给予 l-NAME 会损害自身的记忆检索。相比之下,单独给予一氧化氮(NO)前体 l-精氨酸(0.25 和 0.5μg/rat)没有作用,但可预防尼古丁逆转吗啡对记忆的作用。结果表明,伏隔核内的一氧化氮可能在尼古丁对吗啡诱导的遗忘和吗啡状态依赖记忆的改善作用中发挥作用。