4.5 Article

Multiscale Computer Modeling of Spreading Depolarization in Brain Slices

Journal

ENEURO
Volume 9, Issue 4, Pages -

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/ENEURO.0082-22.2022

Keywords

extracellular space; hypoxia; NEURON; reaction-diffusion; spreading depolarization; spreading depression

Categories

Funding

  1. National Institutes of Health/National Institute of Mental Health [R01-MH-086638]
  2. National Science Foundation Grant Internet2 [E-CAS 1904444]

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The study developed a multiscale computational model of spreading depolarization (SD) in brain slices and made testable predictions regarding the characteristics of SD under different conditions, such as the inhibitory effect of enlarging extracellular space volume on SD and the faster propagation of SD in areas with higher neuronal density.
Spreading depolarization (SD) is a slow-moving wave of neuronal depolarization accompanied by a breakdown of ion concentration homeostasis, followed by long periods of neuronal silence (spreading depression), and is associ-ated with several neurologic conditions. We developed multiscale (ions to tissue slice) computer models of SD in brain slices using the NEURON simulator: 36,000 neurons (two voltage-gated ion channels; three leak channels; three ion exchangers/pumps) in the extracellular space (ECS) of a slice (1 mm sides, varying thicknesses) with ion (K+ , Cl- , Na+) and O-2 diffusion and equilibration with a surrounding bath. Glia and neurons cleared K1 from the ECS via Na+/K+ pumps. SD propagated through the slices at realistic speeds of 2-4 mm/min, which increased by as much as 50% in models incorporating the effects of hypoxia or propionate. In both cases, the speedup was medi-ated principally by ECS shrinkage. Our model allows us to make testable predictions, including the following: (1) SD can be inhibited by enlarging ECS volume; (2) SD velocity will be greater in areas with greater neuronal density, total neuronal volume, or larger/more dendrites; (3) SD is all-or-none: initiating K+ bolus properties have little impact on SD speed; (4) Slice thickness influences SD because of relative hypoxia in the slice core, exacerbated by SD in a pathologic cycle; and (5) SD and high neuronal spike rates will be observed in the core of the slice. Cells in the pe-riphery of the slice near an oxygenated bath will resist SD.

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