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Insights into cerebral haemodynamics and oxygenation utilising in vivo mural cell imaging and mathematical modelling

机译:利用体内壁细胞成像和数学建模洞悉大脑血流动力学和氧合

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摘要

The neurovascular mechanisms underpinning the local regulation of cerebral blood flow (CBF) and oxygen transport remain elusive. In this study we have combined novel in vivo imaging of cortical microvascular and mural cell architecture with mathematical modelling of blood flow and oxygen transport, to provide new insights into CBF regulation that would be inaccessible in a conventional experimental context. Our study indicates that vasoconstriction of smooth muscle actin-covered vessels, rather than pericyte-covered capillaries, induces stable reductions in downstream intravascular capillary and tissue oxygenation. We also propose that seemingly paradoxical observations in the literature around reduced blood velocity in response to arteriolar constrictions might be caused by a propagation of constrictions to upstream penetrating arterioles. We provide support for pericytes acting as signalling conduits for upstream smooth muscle activation, and erythrocyte deformation as a complementary regulatory mechanism. Finally, we caution against the use of blood velocity as a proxy measurement for flow. Our combined imaging-modelling platform complements conventional experimentation allowing cerebrovascular physiology to be probed in unprecedented detail.
机译:支撑脑血流量(CBF)和氧气运输的局部调节的神经血管机制仍然难以捉摸。在这项研究中,我们将皮层微血管和壁细胞结构的新型体内成像与血流和氧气输送的数学模型相结合,以提供对CBF调节的新见解,而在常规实验环境中这是无法获得的。我们的研究表明,平滑肌肌动蛋白覆盖的血管而不是周细胞覆盖的毛细血管的血管收缩引起下游血管内毛细血管和组织氧合的稳定减少。我们还提出,关于响应于小动脉收缩的血流速度降低的文献中看似矛盾的观察可能是由于收缩向上游穿透小动脉的传播所致。我们为周细胞充当上游平滑肌激活的信号传导管道以及红细胞变形作为补充调控机制提供支持。最后,我们告诫不要将血流速度用作流量的替代指标。我们组合的成像建模平台是对常规实验的补充,可对脑血管生理进行前所未有的详细研究。

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