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MK-801 通过 mTOR 信号通路对小鼠海马体抑制性回避记忆的促进作用。

The facilitating effect of MK-801 on inhibitory avoidance memory via mTOR signaling in the mouse hippocampus.

机构信息

Department of Psychology, National Cheng Kung University, Tainan 70101, Taiwan.

Department of Pharmacology, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

Behav Brain Res. 2020 Jul 1;389:112630. doi: 10.1016/j.bbr.2020.112630. Epub 2020 Apr 27.

Abstract

Despite the widespread belief that MK-801 induces memory deficits associated with dementia and schizophrenia in animal models, data regarding the impairing effect of MK-801 on aversive memory have been inconclusive. In this study, we investigated the effect of MK-801 on multiple memory stages of the inhibitory avoidance task, as well as its underlying signaling mechanism in the mouse hippocampus. We successfully replicated a previous finding suggesting that systemic injection of MK-801 impaired memory acquisition, but we observed that an intrahippocampal infusion of MK-801 facilitated the same memory process. We also found that both systemic and intrahippocampal administration of MK-801 facilitated memory consolidation and memory retrieval of the inhibitory avoidance task. We demonstrated that MK-801-induced increases in shock sensitivity and locomotor activity in the pre-training regimen confounded the detrimental effect of MK-801 on memory acquisition, thereby reconciling the inconsistent results in previous studies. In addition, the memory-facilitating effect of MK-801 was found to be dependent on drug dose and shock intensity. We next showed that MK-801 induced a fast-onset increase in the extent of mammalian target of rapamycin (mTOR) phosphorylation in the hippocampus. Finally, we observed that rapamycin, an mTOR inhibitor, blocked both the MK-801-induced increases in phosphorylated mTOR and the facilitating effect of MK-801 on memory consolidation. These results indicate that hippocampal mTOR signaling mediates the facilitating effect of MK-801 on memory consolidation of the inhibitory avoidance task. These findings further imply that MK-801 indeed functions as a memory enhancer and that mTOR signaling serves as a therapeutic target for memory disorders.

摘要

尽管普遍认为 MK-801 在动物模型中会引起与痴呆和精神分裂症相关的记忆缺陷,但关于 MK-801 对厌恶记忆的损害作用的数据尚无定论。在这项研究中,我们研究了 MK-801 对抑制回避任务的多个记忆阶段的影响,以及其在小鼠海马中的潜在信号机制。我们成功复制了先前的发现,即全身注射 MK-801 会损害记忆获得,但我们观察到海马内注射 MK-801 会促进相同的记忆过程。我们还发现,全身和海马内给予 MK-801 均可促进抑制回避任务的记忆巩固和记忆检索。我们证明,MK-801 在预训练方案中引起的电击敏感性和运动活性的增加混淆了 MK-801 对记忆获得的有害影响,从而调和了先前研究中的不一致结果。此外,MK-801 诱导的记忆促进作用被发现取决于药物剂量和电击强度。我们接下来表明,MK-801 诱导了海马中哺乳动物雷帕霉素靶蛋白(mTOR)磷酸化程度的快速起始增加。最后,我们观察到雷帕霉素(一种 mTOR 抑制剂)阻断了 MK-801 诱导的磷酸化 mTOR 的增加以及 MK-801 对记忆巩固的促进作用。这些结果表明,海马 mTOR 信号转导介导了 MK-801 对抑制回避任务记忆巩固的促进作用。这些发现进一步表明,MK-801 确实是一种记忆增强剂,并且 mTOR 信号转导可作为记忆障碍的治疗靶标。

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