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记忆提取过程中记忆印痕的重新激活可预测老年小鼠的长期记忆表现。

Engram reactivation during memory retrieval predicts long-term memory performance in aged mice.

机构信息

Department of Neurobiology, Interdisciplinary Centre for Neurosciences (IZN), Heidelberg University, Heidelberg, Germany.

Department of Neurobiology, Interdisciplinary Centre for Neurosciences (IZN), Heidelberg University, Heidelberg, Germany.

出版信息

Neurobiol Aging. 2021 May;101:256-261. doi: 10.1016/j.neurobiolaging.2021.01.019. Epub 2021 Feb 9.

Abstract

Age-related cognitive decline preferentially targets long-lasting episodic memories that require intact hippocampal function. Memory traces (or engrams) are believed to be encoded within the neurons activated during learning (neuronal ensembles), and recalled by reactivation of the same population. However, whether engram reactivation dictates memory performance late in life is not known. Here, we labeled neuronal ensembles formed during object location recognition learning in the dentate gyrus, and analyzed the reactivation of this population during long-term memory recall in young adult, cognitively impaired- and unimpaired-aged mice. We found that reactivation of memory-encoding neuronal ensembles at long-term memory recall was disrupted in impaired but not unimpaired-aged mice. Furthermore, we showed that the memory performance in the aged population correlated with the degree of engram reactivation at long-term memory recall. Overall, our data implicates recall-induced engram reactivation as a prediction factor of memory performance in aging. Moreover, our findings suggest impairments in neuronal ensemble stabilization and/or reactivation as an underlying mechanism in age-dependent cognitive decline.

摘要

年龄相关的认知衰退优先针对需要完整海马功能的长期情景记忆。记忆痕迹(或记忆印痕)被认为是在学习过程中激活的神经元(神经元集合)中编码的,并通过同一神经元集合的再激活来回忆。然而,记忆印痕的再激活是否决定了晚年的记忆表现尚不清楚。在这里,我们标记了在齿状回中的物体位置识别学习过程中形成的神经元集合,并分析了在年轻成年、认知受损和未受损老年小鼠的长期记忆回忆过程中该集合的再激活情况。我们发现,在认知受损的老年小鼠中,记忆编码神经元集合的再激活在长期记忆回忆中受到了破坏,但在未受损的老年小鼠中则没有。此外,我们还表明,在老年人群体中,记忆表现与长期记忆回忆时记忆印痕的再激活程度相关。总的来说,我们的数据表明,回忆诱导的记忆印痕再激活是衰老过程中记忆表现的一个预测因素。此外,我们的研究结果表明,神经元集合的稳定性和/或再激活受损是年龄相关认知衰退的潜在机制。

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