Malignant astrocyte swelling and impaired glutamate clearance drive the expansion of injurious spreading depolarization foci

Spreading depolarizations (SDs) indicate injury progression and predict worse clinical outcome in acute brain injury. We demonstrate in rodents that acute brain swelling upon cerebral ischemia impairs astroglial glutamate clearance and increases the tissue area invaded by SD. The cytotoxic extracell...

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Elmentve itt :
Bibliográfiai részletek
Szerzők: Menyhárt Ákos
Frank Rita
Farkas Elek Attila
Süle Zoltán
Varga Viktória Éva
Nyúl-Tóth Ádám
Meiller Anne
Ivánkovitsné Kiss Orsolya
Lemale Coline L.
Szabó Írisz
Tóth Réka
Zölei-Szénási Dániel
Woitzik Johannes
Marinesco Stephane
Krizbai István Adorján
Bari Ferenc
Dreier Jens P.
Farkas Eszter
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM 42 No. 4
Tárgyszavak:
doi:10.1177/0271678X211040056

mtmt:32165015
Online Access:http://publicatio.bibl.u-szeged.hu/25658
Leíró adatok
Tartalmi kivonat:Spreading depolarizations (SDs) indicate injury progression and predict worse clinical outcome in acute brain injury. We demonstrate in rodents that acute brain swelling upon cerebral ischemia impairs astroglial glutamate clearance and increases the tissue area invaded by SD. The cytotoxic extracellular glutamate accumulation (>15 mu M) predisposes an extensive bulk of tissue (4-5 mm(2)) for a yet undescribed simultaneous depolarization (SiD). We confirm in rat brain slices exposed to osmotic stress that SiD is the pathological expansion of prior punctual SD foci (0.5-1 mm(2)), is associated with astrocyte swelling, and triggers oncotic neuron death. The blockade of astrocytic aquaporin-4 channels and Na+/K+/Cl- co-transporters, or volume-regulated anion channels mitigated slice edema, extracellular glutamate accumulation (<10 mu M) and SiD occurrence. Reversal of slice swelling by hyperosmotic mannitol counteracted glutamate accumulation and prevented SiD. In contrast, inhibition of glial metabolism or inhibition of astrocyte glutamate transporters reproduced the SiD phenotype. Finally, we show in the rodent water intoxication model of cytotoxic edema that astrocyte swelling and altered astrocyte calcium waves are central in the evolution of SiD. We discuss our results in the light of evidence for SiD in the human cortex. Our results emphasize the need of preventive osmotherapy in acute brain injury.
Terjedelem/Fizikai jellemzők:584-599
ISSN:0271-678X