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阿尔茨海默病小鼠模型中的情景记忆损伤与前额叶-海马区域的过度活跃有关。

Impaired episodic-like memory in a mouse model of Alzheimer's disease is associated with hyperactivity in prefrontal-hippocampal regions.

机构信息

School of Biological Sciences, Nanyang Technological University, Singapore 637551.

Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 308232.

出版信息

Dis Model Mech. 2023 Mar 1;16(3). doi: 10.1242/dmm.049945. Epub 2023 Mar 10.

Abstract

Alzheimer's disease (AD) is a degenerative brain disorder with a long prodromal period. An APPNL-G-F knock-in mouse model is a preclinical model to study incipient pathologies during the early stages of AD. Despite behavioral tests revealing broad cognitive deficits in APPNL-G-F mice, detecting these impairments at the early disease phase has been challenging. In a cognitively demanding task that assessed episodic-like memory, 3-month-old wild-type mice could incidentally form and retrieve 'what-where-when' episodic associations of their past encounters. However, 3-month-old APPNL-G-F mice, corresponding to an early disease stage without prominent amyloid plaque pathology, displayed impairment in recalling 'what-where' information of past episodes. Episodic-like memory is also sensitive to the effect of age. Eight-month-old wild-type mice failed to retrieve conjunctive 'what-where-when' memories. This deficit was also observed in 8-month-old APPNL-G-F mice. c-Fos expression revealed that impaired memory retrieval in APPNL-G-F mice was accompanied by abnormal neuronal hyperactivity in the medial prefrontal cortex and CA1 dorsal hippocampus. These observations can be used for risk stratification during preclinical AD to detect and delay the progression into dementia.

摘要

阿尔茨海默病(AD)是一种退行性脑疾病,具有较长的前驱期。APPNL-G-F 基因敲入小鼠模型是一种临床前模型,可用于研究 AD 早期的初始病理学。尽管行为测试显示 APPNL-G-F 小鼠存在广泛的认知缺陷,但在疾病早期阶段检测到这些缺陷具有挑战性。在一项需要认知能力的情景记忆任务中,3 月龄的野生型小鼠可以偶然地形成和回忆过去经历的“何时何地”情景关联。然而,3 月龄的 APPNL-G-F 小鼠,对应于没有明显淀粉样斑块病理学的早期疾病阶段,在回忆过去事件的“何时何地”信息方面表现出障碍。情景记忆也对年龄的影响敏感。8 月龄的野生型小鼠无法回忆起联合的“何时何地”记忆。APPNL-G-F 小鼠也观察到这种缺陷。c-Fos 表达显示,APPNL-G-F 小鼠的记忆检索受损伴随着内侧前额叶皮层和 CA1 背侧海马的异常神经元过度兴奋。这些观察结果可用于临床前 AD 的风险分层,以检测和延缓痴呆的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a9/10040242/c9244de1eebf/dmm-16-049945-g1.jpg

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