AI Article Synopsis

  • Volume-regulated anion channels (VRACs) help cells manage their volume by allowing the outflow of anions and organic molecules, such as glutamate, especially during conditions like swelling, which often happens during seizures.
  • The study investigated the expression of the VRAC subunit LRRC8A in mesial temporal lobe epilepsy (MTLE) using a specific experimental model, finding that LRRC8A was significantly upregulated in the hippocampus at different time points after inducing epilepsy.
  • The increased levels of LRRC8A in astrocytes and neurons, along with changes in associated glutamate metabolism enzymes, suggest that dysregulated VRAC function may contribute to the development of epilepsy by affecting glutamate dynamics in

Article Abstract

Volume-regulated anion channels (VRACs) are a group of ubiquitously expressed outwardly-rectifying anion channels that sense increases in cell volume and act to return cells to baseline volume through an efflux of anions and organic osmolytes, including glutamate. Because cell swelling, increased extracellular glutamate levels, and reduction of the brain extracellular space (ECS) all occur during seizure generation, we set out to determine whether VRACs are dysregulated throughout mesial temporal lobe epilepsy (MTLE), the most common form of adult epilepsy. To accomplish this, we employed the IHKA experimental model of MTLE, and probed for the expression of LRRC8A, the essential pore-forming VRAC subunit, at acute, early-, mid-, and late-epileptogenic time points (1-, 7-, 14-, and 30-days post-IHKA, respectively). Western blot analysis revealed the upregulation of total dorsal hippocampal LRRC8A 14-days post-IHKA in both the ipsilateral and contralateral hippocampus. Immunohistochemical analyses showed an increased LRRC8A signal 7-days post-IHKA in both the ipsilateral and contralateral hippocampus, along with layer-specific changes 1-, 7-, and 30-days post-IHKA bilaterally. LRRC8A upregulation 1 day post-IHKA was observed primarily in astrocytes; however, some upregulation was also observed in neurons. Glutamate-GABA/glutamine cycle enzymes glutamic acid decarboxylase, glutaminase, and glutamine synthetase were also dysregulated at the 7-day timepoint post status epilepticus. The timepoint-dependent upregulation of total hippocampal LRRC8A and the possible subsequent increased efflux of glutamate in the epileptic hippocampus suggest that the dysregulation of astrocytic VRAC may play an important role in the development of epilepsy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331354PMC
http://dx.doi.org/10.1177/17590914231184072DOI Listing

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