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阿尔茨海默病遗传风险成人中网格细胞样表征减少。

Reduced grid-cell-like representations in adults at genetic risk for Alzheimer's disease.

机构信息

German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany. Department of Epileptology, University of Bonn, Bonn, Germany.

Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, Netherlands.

出版信息

Science. 2015 Oct 23;350(6259):430-3. doi: 10.1126/science.aac8128.

Abstract

Alzheimer's disease (AD) manifests with memory loss and spatial disorientation. AD pathology starts in the entorhinal cortex, making it likely that local neural correlates of spatial navigation, particularly grid cells, are impaired. Grid-cell-like representations in humans can be measured using functional magnetic resonance imaging. We found that young adults at genetic risk for AD (APOE-ε4 carriers) exhibit reduced grid-cell-like representations and altered navigational behavior in a virtual arena. Both changes were associated with impaired spatial memory performance. Reduced grid-cell-like representations were also related to increased hippocampal activity, potentially reflecting compensatory mechanisms that prevent overt spatial memory impairment in APOE-ε4 carriers. Our results provide evidence of behaviorally relevant entorhinal dysfunction in humans at genetic risk for AD, decades before potential disease onset.

摘要

阿尔茨海默病(AD)表现为记忆丧失和空间定向障碍。AD 病理学始于内嗅皮层,因此空间导航的局部神经相关性,特别是网格细胞,很可能受损。可以使用功能磁共振成像来测量人类的网格细胞样表示。我们发现,具有 AD 遗传风险的年轻成年人(APOE-ε4 携带者)在虚拟竞技场中表现出网格细胞样表示的减少和导航行为的改变。这两种变化都与空间记忆表现受损有关。网格细胞样表示的减少也与海马体活动的增加有关,这可能反映了 APOE-ε4 携带者中预防明显空间记忆损伤的代偿机制。我们的研究结果提供了在潜在疾病发作前几十年,具有 AD 遗传风险的人类中与行为相关的内嗅皮层功能障碍的证据。

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