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纵向阿尔茨海默病退化反映了胆碱能基底前脑投射的空间拓扑结构。

Longitudinal Alzheimer's Degeneration Reflects the Spatial Topography of Cholinergic Basal Forebrain Projections.

机构信息

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, QC, Canada.

Medical Research Council Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.

出版信息

Cell Rep. 2018 Jul 3;24(1):38-46. doi: 10.1016/j.celrep.2018.06.001.

Abstract

The cholinergic neurons of the basal forebrain (BF) provide virtually all of the brain's cortical and amygdalar cholinergic input. They are particularly vulnerable to neuropathology in early Alzheimer's disease (AD) and may trigger the emergence of neuropathology in their cortico-amygdalar projection system through cholinergic denervation and trans-synaptic spreading of misfolded proteins. We examined whether longitudinal degeneration within the BF can explain longitudinal cortico-amygdalar degeneration in older human adults with abnormal cerebrospinal fluid biomarkers of AD neuropathology. We focused on two BF subregions, which are known to innervate cortico-amygdalar regions via two distinct macroscopic cholinergic projections. To further assess whether structural degeneration of these regions in AD reflects cholinergic denervation, we used the [F] FEOBV radiotracer, which binds to cortico-amygdalar cholinergic terminals. We found that the two BF subregions explain spatially distinct patterns of cortico-amygdalar degeneration, which closely reflect their cholinergic projections, and overlap with [F] FEOBV indices of cholinergic denervation.

摘要

基底前脑(BF)的胆碱能神经元为大脑皮质和杏仁核提供了几乎所有的胆碱能输入。它们在早期阿尔茨海默病(AD)的神经病理学中特别容易受到影响,并且可能通过胆碱能去神经支配和错误折叠蛋白的跨突触传播触发皮质-杏仁核投射系统的神经病理学出现。我们研究了 BF 内的纵向变性是否可以解释具有 AD 神经病理学异常脑脊液生物标志物的老年人类成年人的纵向皮质-杏仁核变性。我们专注于两个 BF 亚区,它们已知通过两个不同的宏观胆碱能投射来支配皮质-杏仁核区域。为了进一步评估 AD 中这些区域的结构变性是否反映胆碱能去神经支配,我们使用了 [F] FEOBV 示踪剂,它与皮质-杏仁核胆碱能末端结合。我们发现,这两个 BF 亚区解释了皮质-杏仁核变性的空间上不同模式,这些模式与它们的胆碱能投射密切相关,并且与 [F] FEOBV 胆碱能去神经支配指数重叠。

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