Interneurons spark seizure-like activity in the entorhinal cortex

Neurobiol Dis. 2016 Mar:87:91-101. doi: 10.1016/j.nbd.2015.12.011. Epub 2015 Dec 22.

Abstract

Excessive neuronal synchronization is presumably involved in epileptiform synchronization. However, the respective roles played by interneurons (GABAergic) and principal (glutamatergic) cells during interictal and ictal discharges remain unclear. Here, we employed tetrode wire recordings to establish the involvement of these two cell types in 4-aminopyridine-induced interictal- and low-voltage fast (LVF) onset ictal-like discharges in the rat entorhinal cortex in an in vitro slice preparation. We recorded a total of 90 single units (69 putative interneurons, 17 putative principal and 4 unclassified cells) from 36 slices, and found that: (i) interneurons (66.7%) were more likely to fire during interictal discharges than principal cells (35.3%); (ii) interneuron activity increased shortly before LVF ictal onset, whereas principal cell activity did not change; (iii) interneurons and principal cells fired at high rates throughout the tonic phase of the ictal discharge; however, (iv) only interneurons showed phase-locked relationship with LVF activity at 5-15Hz during the tonic phase. Finally, the association of interneuron firing with interictal discharges was maintained during blockade of ionotropic glutamatergic transmission. Our findings demonstrate the prominent involvement of interneurons in interictal discharge generation and in the transition to LVF ictal activity in this in vitro model of epileptiform synchronization.

Keywords: 4-Aminopyridine; Interictal discharges; Interneurons; Low-voltage fast onset ictal discharges; Principal cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Aminopyridine
  • Action Potentials / drug effects
  • Action Potentials / physiology
  • Animals
  • Disease Models, Animal
  • Entorhinal Cortex / drug effects
  • Entorhinal Cortex / physiopathology*
  • Excitatory Amino Acid Antagonists / pharmacology
  • Glutamic Acid / metabolism
  • Interneurons / drug effects
  • Interneurons / physiology*
  • Male
  • Piperazines / pharmacology
  • Quinoxalines / pharmacology
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Seizures / physiopathology*
  • Tissue Culture Techniques

Substances

  • Excitatory Amino Acid Antagonists
  • Piperazines
  • Quinoxalines
  • Receptors, N-Methyl-D-Aspartate
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Glutamic Acid
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid
  • 4-Aminopyridine