Department of Psychology, National Cheng Kung University, Tainan 70101, Taiwan.
Department of Pharmacology, National Cheng Kung University, Tainan 70101, Taiwan.
Behav Brain Res. 2020 Jul 1;389:112630. doi: 10.1016/j.bbr.2020.112630. Epub 2020 Apr 27.
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.
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。