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阿尔茨海默病患者脑血管的病理变化:新视角。

Pathological changes within the cerebral vasculature in Alzheimer's disease: New perspectives.

机构信息

Dementia Research Group, University of Bristol Medical School, Bristol, UK.

出版信息

Brain Pathol. 2022 Nov;32(6):e13061. doi: 10.1111/bpa.13061. Epub 2022 Mar 14.

Abstract

Cerebrovascular disease underpins vascular dementia (VaD), but structural and functional changes to the cerebral vasculature contribute to disease pathology and cognitive decline in Alzheimer's disease (AD). In this review, we discuss the contribution of cerebral amyloid angiopathy and non-amyloid small vessel disease in AD, and the accompanying changes to the density, maintenance and remodelling of vessels (including alterations to the composition and function of the cerebrovascular basement membrane). We consider how abnormalities of the constituent cells of the neurovascular unit - particularly of endothelial cells and pericytes - and impairment of the blood-brain barrier (BBB) impact on the pathogenesis of AD. We also discuss how changes to the cerebral vasculature are likely to impair Aβ clearance - both intra-periarteriolar drainage (IPAD) and transport of Aβ peptides across the BBB, and how impaired neurovascular coupling and reduced blood flow in relation to metabolic demand increase amyloidogenic processing of APP and the production of Aβ. We review the vasoactive properties of Aβ peptides themselves, and the probable bi-directional relationship between vascular dysfunction and Aβ accumulation in AD. Lastly, we discuss recent methodological advances in transcriptomics and imaging that have provided novel insights into vascular changes in AD, and recent advances in assessment of the retina that allow in vivo detection of vascular changes in the early stages of AD.

摘要

脑血管疾病是血管性痴呆(VaD)的基础,但脑血管的结构和功能变化也导致了阿尔茨海默病(AD)的病理和认知能力下降。在这篇综述中,我们讨论了淀粉样血管病和非淀粉样小血管病在 AD 中的作用,以及伴随的血管密度、维持和重塑的变化(包括脑血管基底膜的组成和功能的改变)。我们考虑了神经血管单元的组成细胞(特别是内皮细胞和周细胞)的异常以及血脑屏障(BBB)的损伤如何影响 AD 的发病机制。我们还讨论了脑血管的变化如何可能损害 Aβ 的清除——包括血管周围间隙内的引流(IPAD)和 Aβ 肽穿过 BBB 的转运,以及与代谢需求相关的神经血管耦联障碍和血流量减少如何增加 APP 的淀粉样生成过程和 Aβ 的产生。我们回顾了 Aβ 肽本身的血管活性特性,以及 AD 中血管功能障碍和 Aβ 积累之间可能存在的双向关系。最后,我们讨论了转录组学和影像学方面的最新方法学进展,这些进展为 AD 中的血管变化提供了新的见解,并讨论了评估视网膜的最新进展,这些进展允许在 AD 的早期阶段在体内检测到血管变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884b/9616094/f74ea788bfc3/BPA-32-e13061-g004.jpg

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