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The facilitating effect of MK-801 on inhibitory avoidance memory via mTOR signaling in the mouse hippocampus
Ming-Heng Hsiung1, Wan-Ling Huang1, Li-Yu Kan1
1Department of Psychology, National Cheng Kung University, Tainan 70101, Taiwan.
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.
Insights
MK-801 enhances memory consolidation and retrieval in mice, contrary to popular belief. This memory enhancement is mediated by the mammalian target of rapamycin (mTOR) pathway in the hippocampus.
Area of Science:
- Neuroscience
- Pharmacology
- Cognitive Science
Background:
- MK-801 is widely believed to cause memory deficits, but its effects on aversive memory are debated.
- Previous studies show conflicting results regarding MK-801's impact on memory acquisition.
Purpose of the Study:
- To investigate MK-801's effects on various memory stages (acquisition, consolidation, retrieval) in the inhibitory avoidance task.
- To elucidate the underlying hippocampal signaling mechanisms, particularly the role of mammalian target of rapamycin (mTOR).
Main Methods:
- Systemic and intrahippocampal administration of MK-801 in mice performing an inhibitory avoidance task.
- Assessment of memory acquisition, consolidation, and retrieval.
- Measurement of hippocampal mTOR phosphorylation.
- Inhibition of mTOR signaling using rapamycin.
Main Results:
- Systemic MK-801 impaired acquisition, but intrahippocampal MK-801 facilitated it, resolving previous inconsistencies.
- Both administration routes facilitated memory consolidation and retrieval.
- MK-801 increased hippocampal mTOR phosphorylation, which was blocked by rapamycin.
- Rapamycin also blocked MK-801's memory-enhancing effects on consolidation.
Conclusions:
- MK-801 acts as a memory enhancer, particularly for consolidation and retrieval, mediated by hippocampal mTOR signaling.
- Conflicting results in prior studies are explained by confounding factors like increased shock sensitivity and locomotor activity.
- mTOR signaling represents a potential therapeutic target for memory disorders.
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