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Non-destructive 3D Microtomography of Cerebral Angioarchitecture Changes Following Ischemic Stroke in Rats Using Synchrotron Radiation

机译:同步辐射对大鼠缺血性中风后脑血管结构变化的无损3D显微照相术

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摘要

A better understanding of functional changes in the cerebral microvasculature following ischemic injury is essential to elucidate the pathogenesis of stroke. Up to now, the simultaneous depiction and stereological analysis of 3D micro-architectural changes of brain vasculature with network disorders remains a technical challenge. We aimed to explore the three dimensional (3D) microstructural changes of microvasculature in the rat brain on 4, 6 hours, 3 and 18 days post-ischemia using synchrotron radiation micro-computed tomography (SRμCT) with a per pixel size of 5.2 μm. The plasticity of angioarchitecture was distinctly visualized. Quantitative assessments of time-related trends after focal ischemia, including number of branches, number of nodes, and frequency distribution of vessel diameter, reached a peak at 6 h and significantly decreased at 3 days and initiated to form cavities. The detected pathological changes were also proven by histological tests. We depicted a novel methodology for the 3D analysis of vascular repair in ischemic injury, both qualitatively and quantitatively. Cerebral angioarchitecture sustained 3D remodeling and modification during the healing process. The results might provide a deeper insight into the compensatory mechanisms of microvasculature after injury, suggesting that SRμCT is able to provide a potential new platform for deepening imaging pathological changes in complicated angioarchitecture and evaluating potential therapeutic targets for stroke.
机译:更好地了解缺血性损伤后脑微血管系统的功能变化对于阐明中风的发病机理至关重要。迄今为止,对具有网络障碍的脑血管的3D微结构变化的同时描绘和立体分析仍然是一项技术挑战。我们的目的是使用同步辐射微型计算机断层扫描(SRμCT)探索缺血后4、6、3、18天大鼠大脑微血管的三维(3D)微结构变化,每像素大小为5.2μm。血管结构的可塑性清晰可见。局灶性缺血后与时间相关的趋势的定量评估,包括分支数,结节数和血管直径的频率分布,在6 h达到峰值,在3天时明显下降,并开始形成空腔。通过组织学测试也证实了所检测到的病理变化。我们在定性和定量上描绘了一种用于缺血性损伤中血管修复3D分析的新方法。脑血管结构在愈合过程中持续进行3D重塑和修改。该结果可能为损伤后微脉管的代偿机制提供更深入的见解,这表明SRμCT能够提供一个潜在的新平台,以加深复杂血管结构中的影像病理变化并评估中风的潜在治疗靶标。

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