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多参数光声显微镜揭示清醒小鼠大脑对高碳酸血症的血液动力学和氧代谢反应。

Hemodynamic and oxygen-metabolic responses of the awake mouse brain to hypercapnia revealed by multi-parametric photoacoustic microscopy.

机构信息

Department of Biomedical Engineering, University of Virginia, Charlottesville, VA, USA.

Department of Biology, University of Virginia, Charlottesville, VA, USA.

出版信息

J Cereb Blood Flow Metab. 2021 Oct;41(10):2628-2639. doi: 10.1177/0271678X211010352. Epub 2021 Apr 25.

Abstract

A widely used cerebrovascular stimulus and common pathophysiologic condition, hypercapnia is of great interest in brain research. However, it remains controversial how hypercapnia affects brain hemodynamics and energy metabolism. By using multi-parametric photoacoustic microscopy, the multifaceted responses of the awake mouse brain to different levels of hypercapnia are investigated. Our results show significant and vessel type-dependent increases of the vessel diameter and blood flow in response to the hypercapnic challenges, along with a decrease in oxygen extraction fraction due to elevated venous blood oxygenation. Interestingly, the increased blood flow and decreased oxygen extraction are not commensurate with each other, which leads to reduced cerebral oxygen metabolism. Further, time-lapse imaging over 2-hour chronic hypercapnic challenges reveals that the structural, functional, and metabolic changes induced by severe hypercapnia (10% CO) are not only more pronounced but more enduring than those induced by mild hypercapnia (5% CO), indicating that the extent of brain's compensatory response to chronic hypercapnia is inversely related to the severity of the challenge. Offering quantitative, dynamic, and CO level-dependent insights into the hemodynamic and metabolic responses of the brain to hypercapnia, these findings might provide useful guidance to the application of hypercapnia in brain research.

摘要

高碳酸血症是一种广泛应用于脑血管刺激和常见病理生理状态的方法,在脑研究中具有重要意义。然而,高碳酸血症如何影响脑血液动力学和能量代谢仍然存在争议。通过使用多参数光声显微镜,研究了清醒小鼠大脑对不同水平高碳酸血症的多方面反应。我们的结果表明,血管直径和血流量在高碳酸血症挑战下显著增加,并且由于静脉血氧饱和度升高,氧提取分数降低,这与血管类型有关。有趣的是,增加的血流量和减少的氧提取并不相称,导致脑氧代谢减少。此外,在 2 小时慢性高碳酸血症挑战的时程成像中,揭示了严重高碳酸血症(10% CO)引起的结构、功能和代谢变化不仅更为明显,而且比轻度高碳酸血症(5% CO)引起的变化更为持久,表明大脑对慢性高碳酸血症的代偿反应程度与挑战的严重程度成反比。这些发现为高碳酸血症对大脑的血液动力学和代谢反应提供了定量、动态和 CO 水平依赖性的见解,可能为高碳酸血症在脑研究中的应用提供有用的指导。

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