The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons

Spinal motoneurons may display a variety of firing patterns including bistability between repetitive firing and quiescence and, more rarely, bistability between two firing states of different frequencies. It was suggested in the past that firing bistability required that the persistent L-type calciu...

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Main Authors: Marin eManuel, Daniel eZytnicki, Claude eMeunier
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-01-01
Series:Frontiers in Computational Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00004/full
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spelling doaj-6b2468a40a6540c0a54b38aa537b54c82020-11-24T22:12:42ZengFrontiers Media S.A.Frontiers in Computational Neuroscience1662-51882014-01-01810.3389/fncom.2014.0000474327The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneuronsMarin eManuel0Daniel eZytnicki1Claude eMeunier2Paris Descartes UniversityParis Descartes UniversityParis Descartes UniversitySpinal motoneurons may display a variety of firing patterns including bistability between repetitive firing and quiescence and, more rarely, bistability between two firing states of different frequencies. It was suggested in the past that firing bistability required that the persistent L-type calcium current be segregated in distal dendrites, far away from the spike generating currents. However, this is not supported by more recent data. Using a two compartments model of motoneuron, we show that the different firing patterns may also result from the competition between the more proximal dendritic component of the dendritic L-type conductance and the calcium sensitive potassium conductance responsible for afterhypolarization. This point is further emphasized by showing that firing bistability may be also achieved when the L-type current is put in the somatic compartment of our model. However, this requires that the calcium-sensitive potassium conductance be triggered solely by the high threshold calcium currents activated during spikes and not by calcium influx through the L-type current. This prediction was validated by dynamic clamp experiments in vivo in lumbar motoneurons of deeply anesthetized cats in which an artificial L-type current was added at the soma. Altogether, our results suggest that the dynamical interaction between the L-type and afterhyperpolarization currents is as fundamental as the segregation of the calcium L-type current in dendrites for controling the discharge of motoneurons.<br/>http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00004/fullmodelingafterhyperpolarizationdynamic clampbistabilityPersistent Calcium current
collection DOAJ
language English
format Article
sources DOAJ
author Marin eManuel
Daniel eZytnicki
Claude eMeunier
spellingShingle Marin eManuel
Daniel eZytnicki
Claude eMeunier
The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
Frontiers in Computational Neuroscience
modeling
afterhyperpolarization
dynamic clamp
bistability
Persistent Calcium current
author_facet Marin eManuel
Daniel eZytnicki
Claude eMeunier
author_sort Marin eManuel
title The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
title_short The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
title_full The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
title_fullStr The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
title_full_unstemmed The dendritic location of the L-type current and its deactivation by the somatic AHP current both contribute to firing bistability in motoneurons
title_sort dendritic location of the l-type current and its deactivation by the somatic ahp current both contribute to firing bistability in motoneurons
publisher Frontiers Media S.A.
series Frontiers in Computational Neuroscience
issn 1662-5188
publishDate 2014-01-01
description Spinal motoneurons may display a variety of firing patterns including bistability between repetitive firing and quiescence and, more rarely, bistability between two firing states of different frequencies. It was suggested in the past that firing bistability required that the persistent L-type calcium current be segregated in distal dendrites, far away from the spike generating currents. However, this is not supported by more recent data. Using a two compartments model of motoneuron, we show that the different firing patterns may also result from the competition between the more proximal dendritic component of the dendritic L-type conductance and the calcium sensitive potassium conductance responsible for afterhypolarization. This point is further emphasized by showing that firing bistability may be also achieved when the L-type current is put in the somatic compartment of our model. However, this requires that the calcium-sensitive potassium conductance be triggered solely by the high threshold calcium currents activated during spikes and not by calcium influx through the L-type current. This prediction was validated by dynamic clamp experiments in vivo in lumbar motoneurons of deeply anesthetized cats in which an artificial L-type current was added at the soma. Altogether, our results suggest that the dynamical interaction between the L-type and afterhyperpolarization currents is as fundamental as the segregation of the calcium L-type current in dendrites for controling the discharge of motoneurons.<br/>
topic modeling
afterhyperpolarization
dynamic clamp
bistability
Persistent Calcium current
url http://journal.frontiersin.org/Journal/10.3389/fncom.2014.00004/full
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