Abstract

Computer simulations of external current stimulations of dentate gyrus granule cells of rats with Status Epilepticus induced by pilocarpine and control rats were used to evaluate whether morphological differences alone between these cells have an impact on their electrophysiological behavior. The cell models were constructed using morphological information from tridimensional reconstructions with Neurolucida software. To evaluate the effect of morphology differences alone, ion channel conductances, densities and distributions over the dendritic trees of dentate gyrus granule cells were the same for all models. External simulated currents were injected in randomly chosen dendrites belonging to one of three different areas of dentate gyrus granule cell molecular layer: inner molecular layer, medial molecular layer and outer molecular layer. Somatic membrane potentials were recorded to determine firing frequencies and inter-spike intervals. The results show that morphologically altered granule cells from pilocarpine-induced epileptic rats are less excitable than control cells, especially when they are stimulated in the inner molecular layer, which is the target area for mossy fibers that sprout after pilocarpine-induced cell degeneration. This suggests that morphological alterations may act as a protective mechanism to allow dentate gyrus granule cells to cope with the increase of stimulation caused by mossy fiber sprouting.

Highlights

  • The effects of Status Epilepticus (SE) on neurogenesis of the dentate gyrus (DG) granule cells (GCs) have been widely described [1,2]

  • Our results show that newborn DG GCs from rats with SE induced by PILO are less excitable than newborn DG GCs from control rats

  • In general the compartmental cell models reproduced the responses of actual DG GCs to current step injection with a sequence of spikes with adaptation and no burst [14] (Figures 1A– B)

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Summary

Introduction

The effects of Status Epilepticus (SE) on neurogenesis of the dentate gyrus (DG) granule cells (GCs) have been widely described [1,2]. Those studies report morphological alterations that include modifications of the branching patterns of apical dendrites, presence of basal dendrites that are projected towards the DG hilus, ectopic localization and even dysmorphic presentations [1,3,4,5,6,7,8]. There is evidence of either hyperexcitability [14] or hipoexcitability [15] of GCs in animal models of epilepsy

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