Abstract

Cerebral edema is a major, life threatening complication of ischemic brain damage. Previous studies using brain slices have revealed that cellular swelling and a concomitant increase in tissue transparency starts within minutes of the onset of metabolic insult in association with collective anoxic spreading depolarization (aSD). However, the dynamics of tissue swelling in brain slices under ischemia-like conditions remain elusive. Here, we explored the dynamics of brain tissue swelling induced by oxygen-glucose deprivation (OGD) in submerged rat barrel cortex slices. Video monitoring of the vertical and horizontal position of fluorescent dye-filled neurons and contrast slice surface imaging revealed elevation of the slice surface and a horizontal displacement of the cortical tissue during OGD. The OGD-induced tissue movement was also associated with an expansion of the slice borders. Tissue swelling started several minutes after aSD and continued during reperfusion with normal solution. Thirty minutes after aSD, slice borders had expanded by ~130 μm and the slice surface had moved up to attain a height of ~70 μm above control levels, which corresponded to a volume increase of ~30%. Hyperosmotic sucrose solution partially reduced the OGD-induced slice swelling. Thus, OGD-induced cortical slice tissue swelling in brain slices in vitro recapitulates many features of ischemic cerebral edema in vivo, its onset is tightly linked to aSD and it develops at a relatively slow pace after aSD. We propose that this model of cerebral edema in vitro could be useful for the exploration of the pathophysiological mechanisms underlying ischemic cerebral edema and in the search for an efficient treatment to this devastating condition.

Highlights

  • Cerebral edema is a major life threatening complication of ischemic brain damage (Stokum et al, 2016; Zheng et al, 2016)

  • We found that oxygen-glucose deprivation (OGD) efficiently induces mass tissue movement and swelling that are characteristic of ischemic cerebral edema, that the onset of tissue swelling is tightly linked to anoxic spreading depolarization (aSD) and that it develops on a relatively slow time scale after aSD

  • We studied the dynamics of the tissue shifts and volumetric changes in slices of the rat barrel cortex during ischemia-like conditions induced by OGD

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Summary

Introduction

Cerebral edema is a major life threatening complication of ischemic brain damage (Stokum et al, 2016; Zheng et al, 2016). Cerebral edema is caused by an increase in the brain tissue water content as a result of osmotic changes caused by ionic gradient disturbances and an accumulation of osmotically active metabolites, such as lactate, in the ischemic region (Stokum et al, 2016). Edema develops through several stages starting with cytotoxic edema, or cellular swelling, manifesting minutes after metabolic insult as a result of water translocation from the extracellular to intracellular compartment, generated by the disturbance in the transmembrane ionic gradients during anoxic spreading depolarization (aSD) (Dreier et al, 2018). Cytotoxic edema starts to develop during aSD and it is characterized by swelling of neurons and glial cells, beading of dendrites, shrinkage of the extracellular space, and changes in optical tissue transparency (Vanharreveld, 1957; Murphy et al, 2008; Risher et al, 2009, 2010, 2012). Similar phenomena are observed in submerged cortical slices exposed to oxygen-glucose deprivation (OGD) (Obeidat et al, 2000; Andrew et al, 2007; Risher et al, 2009; Brisson and Andrew, 2012)

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