Cargando…

The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells

Recent studies have shown that stellate cells (SCs) of the medial entorhinal cortex become hyper-excitable in animal models of temporal lobe epilepsy. These studies have also demonstrated the existence of recurrent connections among SCs, reduced levels of recurrent inhibition in epileptic networks a...

Descripción completa

Detalles Bibliográficos
Autores principales: Kispersky, Tilman, White, John A., Rotstein, Horacio G.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2973955/
https://www.ncbi.nlm.nih.gov/pubmed/21079802
http://dx.doi.org/10.1371/journal.pone.0013697
_version_ 1782190852981915648
author Kispersky, Tilman
White, John A.
Rotstein, Horacio G.
author_facet Kispersky, Tilman
White, John A.
Rotstein, Horacio G.
author_sort Kispersky, Tilman
collection PubMed
description Recent studies have shown that stellate cells (SCs) of the medial entorhinal cortex become hyper-excitable in animal models of temporal lobe epilepsy. These studies have also demonstrated the existence of recurrent connections among SCs, reduced levels of recurrent inhibition in epileptic networks as compared to control ones, and comparable levels of recurrent excitation among SCs in both network types. In this work, we investigate the biophysical and dynamic mechanism of generation of the fast time scale corresponding to hyper-excitable firing and the transition between theta and fast firing frequency activity in SCs. We show that recurrently connected minimal networks of SCs exhibit abrupt, threshold-like transition between theta and hyper-excitable firing frequencies as the result of small changes in the maximal synaptic (AMPAergic) conductance. The threshold required for this transition is modulated by synaptic inhibition. Similar abrupt transition between firing frequency regimes can be observed in single, self-coupled SCs, which represent a network of recurrently coupled neurons synchronized in phase, but not in synaptically isolated SCs as the result of changes in the levels of the tonic drive. Using dynamical systems tools (phase-space analysis), we explain the dynamic mechanism underlying the genesis of the fast time scale and the abrupt transition between firing frequency regimes, their dependence on the intrinsic SC's currents and synaptic excitation. This abrupt transition is mechanistically different from others observed in similar networks with different cell types. Most notably, there is no bistability involved. ‘In vitro’ experiments using single SCs self-coupled with dynamic clamp show the abrupt transition between firing frequency regimes, and demonstrate that our theoretical predictions are not an artifact of the model. In addition, these experiments show that high-frequency firing is burst-like with a duration modulated by an M-current.
format Text
id pubmed-2973955
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-29739552010-11-15 The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells Kispersky, Tilman White, John A. Rotstein, Horacio G. PLoS One Research Article Recent studies have shown that stellate cells (SCs) of the medial entorhinal cortex become hyper-excitable in animal models of temporal lobe epilepsy. These studies have also demonstrated the existence of recurrent connections among SCs, reduced levels of recurrent inhibition in epileptic networks as compared to control ones, and comparable levels of recurrent excitation among SCs in both network types. In this work, we investigate the biophysical and dynamic mechanism of generation of the fast time scale corresponding to hyper-excitable firing and the transition between theta and fast firing frequency activity in SCs. We show that recurrently connected minimal networks of SCs exhibit abrupt, threshold-like transition between theta and hyper-excitable firing frequencies as the result of small changes in the maximal synaptic (AMPAergic) conductance. The threshold required for this transition is modulated by synaptic inhibition. Similar abrupt transition between firing frequency regimes can be observed in single, self-coupled SCs, which represent a network of recurrently coupled neurons synchronized in phase, but not in synaptically isolated SCs as the result of changes in the levels of the tonic drive. Using dynamical systems tools (phase-space analysis), we explain the dynamic mechanism underlying the genesis of the fast time scale and the abrupt transition between firing frequency regimes, their dependence on the intrinsic SC's currents and synaptic excitation. This abrupt transition is mechanistically different from others observed in similar networks with different cell types. Most notably, there is no bistability involved. ‘In vitro’ experiments using single SCs self-coupled with dynamic clamp show the abrupt transition between firing frequency regimes, and demonstrate that our theoretical predictions are not an artifact of the model. In addition, these experiments show that high-frequency firing is burst-like with a duration modulated by an M-current. Public Library of Science 2010-11-04 /pmc/articles/PMC2973955/ /pubmed/21079802 http://dx.doi.org/10.1371/journal.pone.0013697 Text en Kispersky et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kispersky, Tilman
White, John A.
Rotstein, Horacio G.
The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title_full The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title_fullStr The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title_full_unstemmed The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title_short The Mechanism of Abrupt Transition between Theta and Hyper-Excitable Spiking Activity in Medial Entorhinal Cortex Layer II Stellate Cells
title_sort mechanism of abrupt transition between theta and hyper-excitable spiking activity in medial entorhinal cortex layer ii stellate cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2973955/
https://www.ncbi.nlm.nih.gov/pubmed/21079802
http://dx.doi.org/10.1371/journal.pone.0013697
work_keys_str_mv AT kisperskytilman themechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells
AT whitejohna themechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells
AT rotsteinhoraciog themechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells
AT kisperskytilman mechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells
AT whitejohna mechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells
AT rotsteinhoraciog mechanismofabrupttransitionbetweenthetaandhyperexcitablespikingactivityinmedialentorhinalcortexlayeriistellatecells