首页> 外文期刊>Journal of Caffeine Research >N-methyl-D-aspartate Receptors Are Involved in Caffeine-Induced Facilitation on Memory Retention of Passive Avoidance Learning in Rats
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N-methyl-D-aspartate Receptors Are Involved in Caffeine-Induced Facilitation on Memory Retention of Passive Avoidance Learning in Rats

机译:N-甲基-D-天冬氨酸受体参与咖啡因诱导的大鼠被动回避学习记忆保持的促进作用。

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Background: Caffeine is an antagonist of adenosine receptors. It preserves cognition and reduces neurodegener-ation. The MK-801, a noncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, has also shown amnesic properties in animal models. Theeffect of caffeine on MK-801-induced amnesia has not been the subject of any recent study.Methods: In this study, the effects of different doses (10 and 30mg/kg) of caffeine on Wistar male rats (eight in each group), passive-avoidance (PA) response, and the impairment of this response by the NMDA receptor antagonist MK-801 (dizocilpine) wereevaluated. The PA response was examined by measuring the step-through latency, 1 and 3 days after the animals received foot-shock training.Results: When given intraperitoneally before the training session, l0mg/kg caffeine elongated the PA response, but 30 mg/kg did not, and it even reduced the step-through latency significantly. Before and after training, administration of 0.2 mg/kg MK-801significantly elongated the PA response. This finding showed that MK-801 had a detrimental effect on learning, consolidation, and memory. We found the first evidence that pre-training and pre-testing administration of 10 mg/kg caffeine significantly reversed the learning and memory consolidation process disrupted by MK-801.Conclusion: These results show an interaction between caffeine and the glutamatergic system, suggesting that low-dose caffeine can prevent learning deficit and amnesia produced by a NMDA antagonist in rats (model of schizophrenia in human) when injectedin pre- and post-training phase and may be clinically useful for treating cognitive impairments in schizophrenia.
机译:背景:咖啡因是腺苷受体的拮抗剂。它保留了认知并减少了神经变性。 MK-801是一种非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,在动物模型中也显示出记忆删除特性。咖啡因对MK-801引起的健忘症的影响尚未成为近期研究的方法。方法:在这项研究中,不同剂量(10和30mg / kg)咖啡因对Wistar雄性大鼠的影响(每组八只)评估了NMDA受体拮抗剂MK-801(地佐西平)的被动回避(PA)反应和该反应的损伤。通过对动物进行足电击训练后的第1天和第3天,通过测量逐步潜伏期来检查PA反应。结果:在训练前腹膜内给予时,10 mg / kg咖啡因延长了PA反应,但30 mg / kg并没有,它甚至大大减少了逐步延迟。训练前后,施用0.2 mg / kg MK-801显着延长了PA反应。这一发现表明,MK-801对学习,巩固和记忆有不利影响。我们发现了第一个证据,即10 mg / kg咖啡因的预训练和预测试给药显着逆转了MK-801破坏的学习和记忆巩固过程。结论:这些结果表明咖啡因与谷氨酸能系统之间存在相互作用,这表明在训练前和训练后阶段注射低剂量咖啡因可预防NMDA拮抗剂在大鼠(人类精神分裂症模型)中产生的学习缺陷和健忘症,在临床上可用于治疗精神分裂症的认知障碍。

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