Suarez Alejandro, Fernandez Lazaro, Riera Jorge
Neuronal Mass Dynamics Lab, Department of Biomedical Engineering, Florida International, University, Miami, FL, USA.
J Cereb Blood Flow Metab. 2025 Jan 10:271678X241311010. doi: 10.1177/0271678X241311010.
Vasoactive signaling from astrocytes is an important contributor to the neurovascular coupling (NVC), which aims at providing energy to neurons during brain activation by increasing blood perfusion in the surrounding vasculature. Pharmacological manipulations have been previously combined with experimental techniques (e.g., transgenic mice, uncaging, and multiphoton microscopy) and stimulation paradigms to isolate individual pathways of the astrocyte-mediated NVC. Unfortunately, these pathways are highly nonlinear and non-additive. To separate these pathways in a unified framework, we combine a comprehensive biophysical model of vasoactive signaling from astrocytes with a unique optogenetic stimulation method that selectively induces astrocytic Ca signaling in a large population of astrocytes. We also use a sensitivity analysis and an optimization technique to estimate key model parameters. Optogenetically-induced Ca signals in astrocytes cause a cerebral blood flow (CBF) response with two major components. Component-1 was rapid and smaller (ΔCBF∼13%, 18 seconds), while component-2 was slowest and highest (ΔCBF ∼18%, 45 seconds). The proposed biophysical model was adequate in reproducing component-2, which was validated with a pharmacological manipulation. Model's predictions were not in contradiction with previous studies. Finally, we discussed scenarios accounting for the existence of component-1, which once validated might be included in our model.
星形胶质细胞的血管活性信号传导是神经血管耦合(NVC)的重要促成因素,神经血管耦合旨在通过增加周围血管系统的血液灌注,在大脑激活期间为神经元提供能量。药理学操作先前已与实验技术(例如,转基因小鼠、光解笼锁和多光子显微镜)以及刺激范式相结合,以分离星形胶质细胞介导的神经血管耦合的各个途径。不幸的是,这些途径具有高度非线性且非相加性。为了在统一框架中分离这些途径,我们将星形胶质细胞血管活性信号传导的综合生物物理模型与一种独特的光遗传学刺激方法相结合,该方法可在大量星形胶质细胞中选择性地诱导星形胶质细胞的钙信号传导。我们还使用敏感性分析和优化技术来估计关键模型参数。星形胶质细胞中光遗传学诱导的钙信号会引起具有两个主要成分的脑血流量(CBF)反应。成分1快速且较小(ΔCBF ∼13%,18秒),而成分2最慢且最高(ΔCBF ∼18%,45秒)。所提出的生物物理模型足以重现成分2,这通过药理学操作得到了验证。模型的预测与先前的研究并不矛盾。最后,我们讨论了解释成分1存在的情况,一旦得到验证,可能会纳入我们的模型。