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Comparison of the effects of acute and chronic administration of ketamine on hippocampal oscillations: relevance for the NMDA receptor hypofunction model of schizophrenia

机译:氯胺酮急慢性给药对海马振荡的影响比较:与精神分裂症的NMDA受体功能低下模型的相关性

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The proper organization and function of GABAergic interneuron networks is essential for many cognitive processes and abnormalities in these systems have been documented in schizophrenic patients. The memory function of the hippocampus depends on two major patterns of oscillations in the theta and gamma ranges, both requiring the intact functioning of the network of fast-firing interneurons expressing parvalbumin. We examined the ability of acute and chronic administration of NMDA receptor (NMDA-R) antagonists to recapitulate the oscillatory dysfunctions observed in schizophrenia. In freely moving rats, acute injection of MK801 or ketamine increased gamma power in both CA1 and dentate gyrus of the hippocampus. Theta peak shifted to higher frequencies whereas the average 5–10 Hz theta power decreased by 24% in CA1 and remained high in the dentate gyrus. Strong increase in CA1 gamma and decrease in theta power triggered by brainstem stimulation were found under urethane anesthesia. In contrast to acute experiments, chronic administration of ketamine caused a steady decline in both gamma and theta oscillations, 2–4 weeks after treatment. A further important difference between the two models was that the effects of acute injection were more robust than the changes after chronic treatment. Chronic administration of ketamine also leads to decrease in the number of detectable parvalbumin interneurons. Histological examination of interindividual differences indicated, however, that within the ketamine treated group a further decrease in parvalbumin neurons correlated with strengthening of oscillations. The findings are consistent with abnormalities of oscillations in human schizophrenia and further validate the NMDA-R hypofunction hypothesis.
机译:GABA能神经元网络的正确组织和功能对于许多认知过程至关重要,并且已在精神分裂症患者中证明了这些系统的异常。海马的记忆功能取决于θ和γ范围内两种主要的振荡模式,两者都需要表达小白蛋白的快中性神经元网络的完整功能。我们检查了急性和慢性给予NMDA受体(NMDA-R)拮抗剂的能力,以概括精神分裂症中观察到的振荡功能障碍。在自由活动的大鼠中,急性注射MK801或氯胺酮会增加CA1和海马齿状回的伽马能。 Theta峰值移到更高的频率,而CA1中5-10 Hz的平均theta功率降低了24%,在齿状回中仍然很高。在氨基甲酸乙酯麻醉下发现脑干刺激引起的CA1γ强烈增加和theta力降低。与急性实验相反,氯胺酮的慢性给药在治疗后2-4周导致γ和theta振荡稳定下降。两种模型之间的另一个重要区别是,急性注射的效果比慢性治疗后的效果更强。氯胺酮的长期给药还导致可检测的小白蛋白中间神经元数量减少。组织学检查的个体差异表明,但是,在氯胺酮治疗组中,小白蛋白神经元的进一步减少与振荡增强有关。这些发现与人类精神分裂症的振荡异常相一致,并进一步验证了NMDA-R功能减退假说。

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