The Edward S. Rogers Sr. Department of Electrical & Computer Engineering, University of Toronto, Toronto, Canada.
Ted Rogers Centre for Heart Research, Translational Biology & Engineering Program, Toronto, Canada.
Sci Rep. 2020 Mar 13;10(1):4705. doi: 10.1038/s41598-020-61682-z.
Compromised microvascular reactivity underlies many conditions and injuries, but its assessment remains difficult, particularly in low perfusion tissues. In this paper, we develop a new mathematical model for the assessment of vasomodulation in low perfusion settings. A first-order model was developed to approximate changes in T relaxation times as a result of vasomodulation. Healthy adult rats (N = 6) were imaged on a 3-Tesla clinical MRI scanner, and vasoactive response was probed on gadofosveset using hypercapnic gases at 20% and 5% CO to induce vasoconstriction and vasodilation, respectively. MRI included dynamic 3D T mapping and T-weighted images during gas challenge; heart rate was continuously monitored. Laser Doppler perfusion measurements were performed to corroborate MRI findings. The model was able to identify hypercapnia-mediated vasoconstriction and vasodilation through the partial derivative [Formula: see text]. MRI on animals revealed gradual vasoconstriction in the skeletal muscle bed in response to 20% CO followed by gradual vasodilation on transitioning to 5% CO. These trends were confirmed on laser Doppler perfusion measurements. Our new mathematical model has the potential for detecting microvascular dysfunction that manifests in the early stages across multiple metabolic and ischemic pathologies.
多种情况下的微血管反应性受损,但其评估仍然具有挑战性,特别是在低灌注组织中。在本文中,我们开发了一种新的数学模型,用于评估低灌注环境下的血管调节。首先开发了一个一阶模型来近似由于血管调节而导致的 T 弛豫时间的变化。在 3 特斯拉临床 MRI 扫描仪上对健康成年大鼠(N = 6)进行成像,并使用高碳酸血症气体在 20%和 5%CO 下分别探测佳呋色特的血管活性反应,以诱导血管收缩和血管舒张。MRI 包括在气体挑战期间的动态 3D T 映射和 T 加权图像;连续监测心率。进行激光多普勒灌注测量以证实 MRI 结果。该模型能够通过偏导数[公式:见文本]来识别高碳酸血症介导的血管收缩和血管舒张。动物 MRI 显示,骨骼肌床在 20%CO 作用下逐渐收缩,随后在过渡到 5%CO 时逐渐舒张。这些趋势在激光多普勒灌注测量上得到了证实。我们的新数学模型有可能检测到在多种代谢和缺血性病理的早期阶段表现出的微血管功能障碍。