Rapid volume pulsations of the extracellular space accompany epileptiform activity in trauma-injured neocortex and depend on the sodium-bicarbonate cotransporter NBCe1

Epilepsy Res. 2024 Mar:201:107337. doi: 10.1016/j.eplepsyres.2024.107337. Epub 2024 Mar 2.

Abstract

Post traumatic epilepsy (PTE) is a treatment-resistant consequence of traumatic brain injury (TBI). Recently, it has been revealed that epileptiform activity in acute chemoconvulsant seizure models is accompanied by transient shrinkages of extracellular space (ECS) called rapid volume pulsations (RVPs). Shrinkage of the ECS surrounding neurons and glia may contribute to ictogenic hyperexcitability and hypersynchrony during the chronic phase of TBI. Here, we identify the phenomenon of RVPs occurring spontaneously in rat neocortex at ≥ 3 weeks after injury in the controlled cortical impact (CCI) model for PTE. We further report that blocking the electrogenic action of the astrocytic cotransporter NBCe1 with 4,4'-diisothiocyano-2,2'-stilbenedisulfonic acid (DIDS) eliminates both RVPs and epileptiform activity in ex-vivo CCI neocortical brain slices. We conclude that NBCe1-mediated extracellular volume shrinkage may represent a new target for therapeutic intervention in PTE.

Keywords: Controlled Cortical Impact; Extracellular Space; NBCe1; Post Traumatic Epilepsy; Probe Transients Quantification; Rapid Volume Pulsation.

MeSH terms

  • Animals
  • Brain Injuries, Traumatic*
  • Epilepsy, Post-Traumatic*
  • Extracellular Space / metabolism
  • Neocortex* / metabolism
  • Rats
  • Sodium-Bicarbonate Symporters / metabolism

Substances

  • Sodium-Bicarbonate Symporters