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阿尔茨海默病转基因小鼠早期皮质血管损伤的证据:光学成像。

Evidence of cortical vascular impairments in early stage of Alzheimer's transgenic mice: Optical imaging.

作者信息

Jeong Hyomin, Pan Yingtian, Akhter Firoz, Volkow Nora D, Zhu Donghui, Du Congwu

机构信息

Department of Biomedical Engineering, State University of New York at Stony Brook, Stony Brook, NY, USA.

National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.

出版信息

J Cereb Blood Flow Metab. 2025 May;45(5):960-976. doi: 10.1177/0271678X241304893. Epub 2024 Dec 18.

Abstract

Alzheimer's disease (AD), a neurodegenerative disorder with progressive cognitive decline, remains clinically challenging with limited understanding of etiology and interventions. Clinical studies have reported vascular defects prior to other pathological manifestations of AD, leading to the "Vascular Hypothesis" for the disorder. However, assessments of cerebral vasculature in AD rodent models have been constrained by limited spatiotemporal resolution or field of view of conventional imaging. We herein employed two imaging technologies, Dual-Wavelength Imaging and Optical Coherence Doppler Tomography, to evaluate cerebrovascular reactivity (CVR) to vasoconstrictive cocaine and vasodilatory hypercapnia challenges and to detect resting 3D cerebral blood flow (CBF) in living transgenic AD mice at capillary resolution. Results showed that CVR to cocaine and hypercapnia was significantly attenuated in 7-10 months old AD mice vs controls, indicating reduced vascular flexibility and reactivity. Additionally, in the AD mice, arterial CBF velocities were slower and the microvascular density in cortex was decreased compared to controls. These results reveal significant vascular impairments including reduced CVR and resting CBF in early-staged AD mice. Hence, this cutting-edge optical imaging offers an innovative venue for detecting early neurovascular dysfunction in AD brain with translational potential.

摘要

阿尔茨海默病(AD)是一种伴有进行性认知衰退的神经退行性疾病,由于对其病因和干预措施的了解有限,在临床上仍然具有挑战性。临床研究报告称,在AD的其他病理表现出现之前就存在血管缺陷,从而产生了该疾病的“血管假说”。然而,AD啮齿动物模型中脑血管系统的评估受到传统成像有限的时空分辨率或视野的限制。我们在此采用了两种成像技术,即双波长成像和光学相干多普勒断层扫描,以评估脑血管对血管收缩剂可卡因和血管舒张剂高碳酸血症刺激的反应性(CVR),并在活体转基因AD小鼠中以毛细血管分辨率检测静息状态下的三维脑血流量(CBF)。结果显示,与对照组相比,7至10月龄AD小鼠对可卡因和高碳酸血症的CVR显著减弱,表明血管弹性和反应性降低。此外,与对照组相比,AD小鼠的动脉CBF速度较慢,皮质微血管密度降低。这些结果揭示了早期AD小鼠存在显著的血管损伤,包括CVR降低和静息CBF减少。因此,这种前沿的光学成像为检测AD大脑早期神经血管功能障碍提供了一个具有转化潜力的创新途径。

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