Potassium channels-mediated electrophysiologic responses are inhibited by cytosolic phospholipase A2α ablation

Neuroreport. 2018 Jan 3;29(1):59-64. doi: 10.1097/WNR.0000000000000933.

Abstract

Cytosolic phospholipase A2α (cPLA2α) is implicated in the progression of excitotoxic neuronal injury and cerebral ischemia. Previous work suggests that cPLA2α increases aberrant electrophysiologic events through attenuating K channel functions. Nevertheless, which K channels are affected by cPLA2α needs to be determined. Here we examined K channels-mediated electrophysiologic responses in hippocampal CA1 pyramidal neurons from wild-type and cPLA2α mice using simultaneous patch-clamp recording and confocal Ca imaging. After the exposure to the blockers of Ca-sensitive and A-type K channels, all CA1 neurons developed spike broadening and increased dendritic Ca transients. These effects were occluded in CA1 neurons from cPLA2α mice. Therefore, cPLA2α modulates the functions of Ca-sensitive and A-type K channels in neurotoxicity.

MeSH terms

  • 2S Albumins, Plant / genetics
  • 2S Albumins, Plant / metabolism*
  • 4-Aminopyridine / pharmacology
  • Action Potentials / drug effects
  • Action Potentials / genetics
  • Animals
  • Apamin / pharmacology
  • Calcium / metabolism
  • Electric Stimulation
  • Electrophysiological Phenomena
  • Hippocampus / cytology*
  • In Vitro Techniques
  • Mice
  • Mice, Transgenic
  • Patch-Clamp Techniques
  • Paxillin / pharmacology
  • Potassium Channel Blockers / pharmacology
  • Potassium Channels / metabolism*
  • Pyramidal Cells / drug effects
  • Pyramidal Cells / metabolism*

Substances

  • 2S Albumins, Plant
  • Paxillin
  • Potassium Channel Blockers
  • Potassium Channels
  • pea seed albumin 2
  • Apamin
  • 4-Aminopyridine
  • Calcium