» Articles » PMID: 39791314

Characterizing Astrocyte-mediated Neurovascular Coupling by Combining Optogenetics and Biophysical Modeling

Overview
Publisher Sage Publications
Date 2025 Jan 10
PMID 39791314
Authors
Affiliations
Soon will be listed here.
Abstract

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.

References
1.
Krawchuk M, Ruff C, Yang X, Ross S, Vazquez A . Optogenetic assessment of VIP, PV, SOM and NOS inhibitory neuron activity and cerebral blood flow regulation in mouse somato-sensory cortex. J Cereb Blood Flow Metab. 2019; 40(7):1427-1440. PMC: 7307010. DOI: 10.1177/0271678X19870105. View

2.
Peng X, Zhang C, Alkayed N, Harder D, Koehler R . Dependency of cortical functional hyperemia to forepaw stimulation on epoxygenase and nitric oxide synthase activities in rats. J Cereb Blood Flow Metab. 2004; 24(5):509-17. DOI: 10.1097/00004647-200405000-00004. View

3.
Toth P, Csiszar A, Tucsek Z, Sosnowska D, Gautam T, Koller A . Role of 20-HETE, TRPC channels, and BKCa in dysregulation of pressure-induced Ca2+ signaling and myogenic constriction of cerebral arteries in aged hypertensive mice. Am J Physiol Heart Circ Physiol. 2013; 305(12):H1698-708. PMC: 3882550. DOI: 10.1152/ajpheart.00377.2013. View

4.
Shim H, Jung W, Schlegel F, Lee J, Kim S, Lee J . Mouse fMRI under ketamine and xylazine anesthesia: Robust contralateral somatosensory cortex activation in response to forepaw stimulation. Neuroimage. 2018; 177:30-44. DOI: 10.1016/j.neuroimage.2018.04.062. View

5.
Keller D, Ero C, Markram H . Cell Densities in the Mouse Brain: A Systematic Review. Front Neuroanat. 2018; 12:83. PMC: 6205984. DOI: 10.3389/fnana.2018.00083. View