Literature DB >> 25122714

Minimum conditions for the induction of cortical spreading depression in brain slices.

Yujie T Tang1, Jorge M Mendez2, Jeremy J Theriot2, Punam M Sawant2, Héctor E López-Valdés3, Y Sungtaek Ju1, K C Brennan4.   

Abstract

Cortical spreading depression (CSD) occurs during various forms of brain injury such as stroke, subarachnoid hemorrhage, and brain trauma, but it is also thought to be the mechanism of the migraine aura. It is therefore expected to occur over a range of conditions including the awake behaving state. Yet it is unclear how such a massive depolarization could occur under relatively benign conditions. Using a microfluidic device with focal stimulation capability in a mouse brain slice model, we varied extracellular potassium concentration as well as the area exposed to increased extracellular potassium to determine the minimum conditions necessary to elicit CSD. Importantly, we focused on potassium levels that are physiologically plausible (≤145 mM; the intracellular potassium concentration). We found a strong correlation between the threshold concentration and the slice area exposed to increased extracellular potassium: minimum area of exposure was needed with the highest potassium concentration, while larger areas were needed at lower concentrations. We also found that moderate elevations of extracellular potassium were able to elicit CSD in relatively small estimated tissue volumes that might be activated under noninjury conditions. Our results thus show that CSD may be inducible under the conditions that expected in migraine aura as well as those related to brain trauma.
Copyright © 2014 the American Physiological Society.

Entities:  

Keywords:  cortical spreading depression; microfluidics; migraine

Mesh:

Substances:

Year:  2014        PMID: 25122714      PMCID: PMC4233272          DOI: 10.1152/jn.00205.2014

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  53 in total

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4.  The minimum volume of depolarized neural tissue required for triggering cortical spreading depression in rat.

Authors:  T Matsuura; J Bures
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5.  A nosographic analysis of the migraine aura in a general population.

Authors:  M B Russell; J Olesen
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6.  Spreading depression in elasmobranch cerebellum.

Authors:  W Young
Journal:  Brain Res       Date:  1980-10-13       Impact factor: 3.252

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Authors:  C Nicholson
Journal:  J Neurosci Methods       Date:  1993-07       Impact factor: 2.390

9.  Focal hyperemia followed by spreading oligemia and impaired activation of rCBF in classic migraine.

Authors:  J Olesen; B Larsen; M Lauritzen
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10.  Suppression of spreading depression-like events in locusts by inhibition of the NO/cGMP/PKG pathway.

Authors:  Gary A B Armstrong; Corinne I Rodgers; Tomas G A Money; R Meldrum Robertson
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  19 in total

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Review 2.  The continuum of spreading depolarizations in acute cortical lesion development: Examining Leão's legacy.

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Review 3.  Microphysiological Human Brain and Neural Systems-on-a-Chip: Potential Alternatives to Small Animal Models and Emerging Platforms for Drug Discovery and Personalized Medicine.

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4.  Spreading depolarization and neuronal damage or survival in mouse neocortical brain slices immediately and 12 hours following middle cerebral artery occlusion.

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Review 5.  Spreading Depression, Spreading Depolarizations, and the Cerebral Vasculature.

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6.  Heterogeneous incidence and propagation of spreading depolarizations.

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7.  Susceptibility of Primary Sensory Cortex to Spreading Depolarizations.

Authors:  Volodymyr B Bogdanov; Natalie A Middleton; Jeremy J Theriot; Patrick D Parker; Osama M Abdullah; Y Sungtaek Ju; Jed A Hartings; K C Brennan
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Review 8.  Involvement of extrasynaptic glutamate in physiological and pathophysiological changes of neuronal excitability.

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Journal:  J Cereb Blood Flow Metab       Date:  2016-01-01       Impact factor: 6.200

Review 10.  Cortical spreading depression: culprits and mechanisms.

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Journal:  Exp Brain Res       Date:  2022-01-22       Impact factor: 1.972

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