The antiseizure medication valproate increases hemichannel activity found in brain cells, which could worsen disease outcomes

J Neurochem. 2024 Jun;168(6):1045-1059. doi: 10.1111/jnc.16062. Epub 2024 Jan 30.

Abstract

Glial cells play relevant roles in neuroinflammation caused by epilepsy. Elevated hemichannel (HC) activity formed by connexins (Cxs) or pannexin1 (Panx1) largely explains brain dysfunctions commonly caused by neuroinflammation. Glia express HCs formed by Cxs 43, 30, or 26, while glia and neurons both express HCs formed by Panx1. Cx43 HCs allow for the influx of Ca2+, which promotes glial reactivity, enabling the release of the gliotransmitters that contribute to neuronal over-stimulation. Valproate (VPA), an antiseizure medication, has pleiotropic actions on neuronal molecular targets, and their action on glial cell HCs remains elusive. We used HeLa cells transfected with Cx43, Cx30, Cx26, or Panx1 to determine the effect of VPA on HC activity in the brain. VPA slightly increased HC activity under basal conditions, but significantly enhanced it in cells pre-exposed to conditions that promoted HC activity. Furthermore, VPA increased ATP release through Cx43 HCs. The increased HC activity caused by VPA was resistant to washout, being consistent with in silico studies, which predicted the binding site for VPA and Cx43, as well as for Panx1 HCs on the intracellular side, suggesting that VPA first enters through HCs, after which their activity increases.

Keywords: connexons; epilepsy; neuroinflammation; pannexons; valproic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Anticonvulsants* / pharmacology
  • Brain / drug effects
  • Brain / metabolism
  • Connexin 43 / metabolism
  • Connexins* / metabolism
  • Epilepsy / chemically induced
  • Epilepsy / drug therapy
  • Epilepsy / metabolism
  • HeLa Cells
  • Humans
  • Nerve Tissue Proteins / metabolism
  • Neuroglia / drug effects
  • Neuroglia / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • Valproic Acid* / pharmacology

Substances

  • Valproic Acid
  • Anticonvulsants
  • Connexins
  • Connexin 43
  • Nerve Tissue Proteins
  • Adenosine Triphosphate
  • PANX1 protein, human