Abstract

BackgroundPrevious studies from animal models have shown that pre-synaptic NMDA receptors (preNMDARs) are present in the cortex, but the role of inhibition mediated by preNMDARs during epileptogenesis remains unclear. In this study, we wanted to observe the changes in GABAergic inhibition through preNMDARs in sensory-motor and visual cortical pyramidal neurons after pilocarpine-induced status epilepticus.MethodsUsing a pilocarpine-induced epileptic mouse model, sensory-motor and visual cortical slices were prepared, and the whole-cell patch clamp technique was used to record spontaneous inhibitory post-synaptic currents (sIPSCs).ResultsThe primary finding was that the mean amplitude of sIPSC from the sensory-motor cortex increased significantly in epileptic mice when the recording pipette contained MK-801 compared to control mice, whereas the mean sIPSC frequency was not significantly different, indicating that post-synaptic mechanisms are involved. However, there was no significant pre-synaptic inhibition through preNMDARs in the acute brain slices from pilocarpine-induced epileptic mice.ConclusionIn the acute case of epilepsy, a compensatory mechanism of post-synaptic inhibition, possibly from ambient GABA, was observed through changes in the amplitude without significant changes in the frequency of sIPSC compared to control mice. The role of preNMDAR-mediated inhibition in epileptogenesis during the chronic condition or in the juvenile stage warrants further investigation.

Highlights

  • The incidence of epilepsy in children is consistently reported to be highest in the first year of life [1]

  • The aim of this study was to record the amplitude, frequency and kinetic properties of spontaneous inhibitory post-synaptic currents in the sensory-motor and visual cortices of the mouse model in the inhibitory synapses of pyramidal neurons to discover the role of the pre-synaptic NMDA receptor in epilepsy

  • The hypothesis was that the synaptic transmission of GABA might be changed in an underlying mechanism of epileptogenesis through pre-synaptic NMDA receptors mediated by calcium (Ca2+) influx in young mice

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Summary

Introduction

The incidence of epilepsy in children is consistently reported to be highest in the first year of life [1]. In terms of age of animal models compared to human, there have been a number of efforts to correlate the age of the animal with human years [2, 3]. This correlation means that the age of a 20–30-day-old rodent used in the current study is equal to 1–2 years in a human or an infant. Several studies have shown an increase in the density of hippocampal and cortical NMDA receptors (NMDARs) in certain animal models of epilepsy [5, 6]. Previous studies from animal models have shown that pre-synaptic NMDA receptors (preNMDARs) are present in the cortex, but the role of inhibition mediated by preNMDARs during epileptogenesis remains unclear. We wanted to observe the changes in GABAergic inhibition through preNMDARs in sensory-motor and visual cortical pyramidal neurons after pilocarpine-induced status epilepticus

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