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The Roles of Potassium and Calcium Currents in the Bistable Firing Transition

Healthy brains display a wide range of firing patterns, from synchronized oscillations during slow-wave sleep to desynchronized firing during movement. These physiological activities coexist with periods of pathological hyperactivity in the epileptic brain, where neurons can fire in synchronized bur...

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Autores principales: Borges, Fernando S., Protachevicz, Paulo R., Souza, Diogo L. M., Bittencourt, Conrado F., Gabrick, Enrique C., Bentivoglio, Lucas E., Szezech, José D., Batista, Antonio M., Caldas, Iberê L., Dura-Bernal, Salvador, Pena, Rodrigo F. O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10527161/
https://www.ncbi.nlm.nih.gov/pubmed/37759949
http://dx.doi.org/10.3390/brainsci13091347
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author Borges, Fernando S.
Protachevicz, Paulo R.
Souza, Diogo L. M.
Bittencourt, Conrado F.
Gabrick, Enrique C.
Bentivoglio, Lucas E.
Szezech, José D.
Batista, Antonio M.
Caldas, Iberê L.
Dura-Bernal, Salvador
Pena, Rodrigo F. O.
author_facet Borges, Fernando S.
Protachevicz, Paulo R.
Souza, Diogo L. M.
Bittencourt, Conrado F.
Gabrick, Enrique C.
Bentivoglio, Lucas E.
Szezech, José D.
Batista, Antonio M.
Caldas, Iberê L.
Dura-Bernal, Salvador
Pena, Rodrigo F. O.
author_sort Borges, Fernando S.
collection PubMed
description Healthy brains display a wide range of firing patterns, from synchronized oscillations during slow-wave sleep to desynchronized firing during movement. These physiological activities coexist with periods of pathological hyperactivity in the epileptic brain, where neurons can fire in synchronized bursts. Most cortical neurons are pyramidal regular spiking (RS) cells with frequency adaptation and do not exhibit bursts in current-clamp experiments (in vitro). In this work, we investigate the transition mechanism of spike-to-burst patterns due to slow potassium and calcium currents, considering a conductance-based model of a cortical RS cell. The joint influence of potassium and calcium ion channels on high synchronous patterns is investigated for different synaptic couplings ([Formula: see text]) and external current inputs (I). Our results suggest that slow potassium currents play an important role in the emergence of high-synchronous activities, as well as in the spike-to-burst firing pattern transitions. This transition is related to the bistable dynamics of the neuronal network, where physiological asynchronous states coexist with pathological burst synchronization. The hysteresis curve of the coefficient of variation of the inter-spike interval demonstrates that a burst can be initiated by firing states with neuronal synchronization. Furthermore, we notice that high-threshold ([Formula: see text]) and low-threshold ([Formula: see text]) ion channels play a role in increasing and decreasing the parameter conditions ([Formula: see text] and I) in which bistable dynamics occur, respectively. For high values of [Formula: see text] conductance, a synchronous burst appears when neurons are weakly coupled and receive more external input. On the other hand, when the conductance [Formula: see text] increases, higher coupling and lower I are necessary to produce burst synchronization. In light of our results, we suggest that channel subtype-specific pharmacological interactions can be useful to induce transitions from pathological high bursting states to healthy states.
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spelling pubmed-105271612023-09-28 The Roles of Potassium and Calcium Currents in the Bistable Firing Transition Borges, Fernando S. Protachevicz, Paulo R. Souza, Diogo L. M. Bittencourt, Conrado F. Gabrick, Enrique C. Bentivoglio, Lucas E. Szezech, José D. Batista, Antonio M. Caldas, Iberê L. Dura-Bernal, Salvador Pena, Rodrigo F. O. Brain Sci Article Healthy brains display a wide range of firing patterns, from synchronized oscillations during slow-wave sleep to desynchronized firing during movement. These physiological activities coexist with periods of pathological hyperactivity in the epileptic brain, where neurons can fire in synchronized bursts. Most cortical neurons are pyramidal regular spiking (RS) cells with frequency adaptation and do not exhibit bursts in current-clamp experiments (in vitro). In this work, we investigate the transition mechanism of spike-to-burst patterns due to slow potassium and calcium currents, considering a conductance-based model of a cortical RS cell. The joint influence of potassium and calcium ion channels on high synchronous patterns is investigated for different synaptic couplings ([Formula: see text]) and external current inputs (I). Our results suggest that slow potassium currents play an important role in the emergence of high-synchronous activities, as well as in the spike-to-burst firing pattern transitions. This transition is related to the bistable dynamics of the neuronal network, where physiological asynchronous states coexist with pathological burst synchronization. The hysteresis curve of the coefficient of variation of the inter-spike interval demonstrates that a burst can be initiated by firing states with neuronal synchronization. Furthermore, we notice that high-threshold ([Formula: see text]) and low-threshold ([Formula: see text]) ion channels play a role in increasing and decreasing the parameter conditions ([Formula: see text] and I) in which bistable dynamics occur, respectively. For high values of [Formula: see text] conductance, a synchronous burst appears when neurons are weakly coupled and receive more external input. On the other hand, when the conductance [Formula: see text] increases, higher coupling and lower I are necessary to produce burst synchronization. In light of our results, we suggest that channel subtype-specific pharmacological interactions can be useful to induce transitions from pathological high bursting states to healthy states. MDPI 2023-09-20 /pmc/articles/PMC10527161/ /pubmed/37759949 http://dx.doi.org/10.3390/brainsci13091347 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Borges, Fernando S.
Protachevicz, Paulo R.
Souza, Diogo L. M.
Bittencourt, Conrado F.
Gabrick, Enrique C.
Bentivoglio, Lucas E.
Szezech, José D.
Batista, Antonio M.
Caldas, Iberê L.
Dura-Bernal, Salvador
Pena, Rodrigo F. O.
The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title_full The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title_fullStr The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title_full_unstemmed The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title_short The Roles of Potassium and Calcium Currents in the Bistable Firing Transition
title_sort roles of potassium and calcium currents in the bistable firing transition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10527161/
https://www.ncbi.nlm.nih.gov/pubmed/37759949
http://dx.doi.org/10.3390/brainsci13091347
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