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阿尔茨海默病动物模型体内神经元功能的阶段性衰退。

Staged decline of neuronal function in vivo in an animal model of Alzheimer's disease.

机构信息

Institute of Neuroscience and Center for Integrated Protein Science, Technical University Munich, Biedersteinerstr. 29, 80802 Munich, Germany.

出版信息

Nat Commun. 2012 Apr 10;3:774. doi: 10.1038/ncomms1783.

Abstract

The accumulation of amyloid-β in the brain is an essential feature of Alzheimer's disease. However, the impact of amyloid-β-accumulation on neuronal dysfunction on the single cell level in vivo is poorly understood. Here we investigate the progression of amyloid-β load in relation to neuronal dysfunction in the visual system of the APP23×PS45 mouse model of Alzheimer's disease. Using in vivo two-photon calcium imaging in the visual cortex, we demonstrate that a progressive deterioration of neuronal tuning for the orientation of visual stimuli occurs in parallel with the age-dependent increase of the amyloid-β load. Importantly, we find this deterioration only in neurons that are hyperactive during spontaneous activity. This impairment of visual cortical circuit function also correlates with pronounced deficits in visual-pattern discrimination. Together, our results identify distinct stages of decline in sensory cortical performance in vivo as a function of the increased amyloid-β-load.

摘要

淀粉样蛋白-β在大脑中的积累是阿尔茨海默病的一个重要特征。然而,淀粉样蛋白-β积累对体内单个神经元功能障碍的影响在很大程度上仍不清楚。在这里,我们研究了 APP23×PS45 阿尔茨海默病小鼠模型的视觉系统中淀粉样蛋白-β负荷与神经元功能障碍的进展关系。通过在视觉皮层进行体内双光子钙成像,我们证明了神经元对视觉刺激方向的调谐逐渐恶化与淀粉样蛋白-β负荷的年龄依赖性增加平行发生。重要的是,我们仅在自发活动期间过度活跃的神经元中发现这种恶化。这种视觉皮层回路功能的损害也与视觉模式识别的明显缺陷相关。总之,我们的研究结果确定了随着淀粉样蛋白-β负荷的增加,体内感觉皮层性能下降的不同阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1670/3337977/7adc6ca7e7df/ncomms1783-f1.jpg

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