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早期检测个体小鼠与年龄相关的记忆缺陷。

Early detection of age-related memory deficits in individual mice.

机构信息

ENMVI team, UMR CNRS 7102, Université P&M Curie, F-75005 Paris, France.

出版信息

Neurobiol Aging. 2011 Oct;32(10):1881-95. doi: 10.1016/j.neurobiolaging.2009.11.001. Epub 2009 Dec 9.

Abstract

To date, no consensus has been reached concerning the age of the earliest onset of age-related cognitive deficits in rodents. Our aim was to develop a behavioral model allowing early and individual detection of age-related cognitive impairments. We tested young (3 months), middle-aged (10 months) and aged (17 months) C57Bl/6 mice in the starmaze, a task allowing precise analysis of the search pattern of mice via standardized calculation of two navigation indices. We performed mouse-per-mouse analyses and compared each mouse's performance to a threshold based on young mice's performances. Using this method we identified impaired mice from the age of 10 months old. Their deficits were independent of any sensorimotor dysfunctions and were associated with an alteration of the maintenance of the hippocampal CA1 late-LTP. This study develops reliable methodology for early detection of age-related memory disorders and provides evidence that memory can decline in some individuals as early as from the age of 10 months.

摘要

迄今为止,关于啮齿动物与年龄相关的认知缺陷最早出现的年龄,尚未达成共识。我们的目的是开发一种行为模型,允许早期和个体检测与年龄相关的认知障碍。我们在星形迷宫中测试了年轻(3 个月)、中年(10 个月)和老年(17 个月)C57Bl/6 小鼠,该任务允许通过标准化计算两个导航指数,精确分析小鼠的搜索模式。我们对每只老鼠进行老鼠对老鼠的分析,并将每只老鼠的表现与基于年轻老鼠表现的阈值进行比较。使用这种方法,我们从 10 个月大时就发现了受损的老鼠。它们的缺陷与任何感觉运动功能障碍无关,与海马 CA1 晚期长时程增强的维持改变有关。这项研究开发了可靠的方法,用于早期检测与年龄相关的记忆障碍,并提供了证据,表明记忆力早在 10 个月大时就可能在某些个体中下降。

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