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使用对比增强磁共振血管造影术检测正常衰老C57BL/6小鼠大脑中的脑血管损失

Detection of Cerebrovascular Loss in the Normal Aging C57BL/6 Mouse Brain Using Contrast-Enhanced Magnetic Resonance Angiography.

作者信息

Hill Lindsay K, Hoang Dung Minh, Chiriboga Luis A, Wisniewski Thomas, Sadowski Martin J, Wadghiri Youssef Z

机构信息

Department of Chemical and Biomolecular Engineering, NYU Tandon School of Engineering, Brooklyn, NY, United States.

Department of Radiology, Center for Advanced Imaging Innovation and Research (CAI2R), NYU Grossman School of Medicine, New York, NY, United States.

出版信息

Front Aging Neurosci. 2020 Oct 20;12:585218. doi: 10.3389/fnagi.2020.585218. eCollection 2020.

Abstract

Microvascular rarefaction, or the decrease in vascular density, has been described in the cerebrovasculature of aging humans, rats, and, more recently, mice in the presence and absence of age-dependent diseases. Given the wide use of mice in modeling age-dependent human diseases of the cerebrovasculature, visualization, and quantification of the global murine cerebrovasculature is necessary for establishing the baseline changes that occur with aging. To provide whole-brain imaging of the cerebrovasculature in aging C57BL/6 mice longitudinally, contrast-enhanced magnetic resonance angiography (CE-MRA) was employed using a house-made gadolinium-bearing micellar blood pool agent. Enhancement in the vascular space permitted quantification of the detectable, or apparent, cerebral blood volume (aCBV), which was analyzed over 2 years of aging and compared to histological analysis of the cerebrovascular density. A significant loss in the aCBV was detected by CE-MRA over the aging period. Histological analysis vessel-probing immunohistochemistry confirmed a significant loss in the cerebrovascular density over the same 2-year aging period, validating the CE-MRA findings. While these techniques use widely different methods of assessment and spatial resolutions, their comparable findings in detected vascular loss corroborate the growing body of literature describing vascular rarefaction aging. These findings suggest that such age-dependent changes can contribute to cerebrovascular and neurodegenerative diseases, which are modeled using wild-type and transgenic laboratory rodents.

摘要

微血管稀疏,即血管密度降低,已在衰老的人类、大鼠以及最近在有和没有年龄依赖性疾病的小鼠的脑血管系统中被描述。鉴于小鼠在模拟年龄依赖性人类脑血管疾病方面的广泛应用,对全球小鼠脑血管系统进行可视化和量化对于确定衰老过程中发生的基线变化是必要的。为了纵向提供衰老的C57BL/6小鼠脑血管系统的全脑成像,使用自制的含钆胶束血池剂进行对比增强磁共振血管造影(CE-MRA)。血管空间的增强允许对可检测到的或表观的脑血容量(aCBV)进行量化,在两年的衰老过程中对其进行分析,并与脑血管密度的组织学分析进行比较。在衰老期间,CE-MRA检测到aCBV显著下降。组织学分析——血管探测免疫组织化学证实,在相同的两年衰老期内,脑血管密度显著下降,验证了CE-MRA的结果。虽然这些技术使用了广泛不同的评估方法和空间分辨率,但它们在检测到的血管损失方面的可比结果证实了越来越多描述血管稀疏衰老的文献。这些发现表明,这种年龄依赖性变化可能导致脑血管疾病和神经退行性疾病,而这些疾病是使用野生型和转基因实验啮齿动物进行建模的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b617/7606987/25db0076e3c9/fnagi-12-585218-g0001.jpg

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