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Thalamic neuron models encode stimulus information by burst-size modulation

Thalamic neurons have been long assumed to fire in tonic mode during perceptive states, and in burst mode during sleep and unconsciousness. However, recent evidence suggests that bursts may also be relevant in the encoding of sensory information. Here, we explore the neural code of such thalamic bur...

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Autores principales: Elijah, Daniel H., Samengo, Inés, Montemurro, Marcelo A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585143/
https://www.ncbi.nlm.nih.gov/pubmed/26441623
http://dx.doi.org/10.3389/fncom.2015.00113
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author Elijah, Daniel H.
Samengo, Inés
Montemurro, Marcelo A.
author_facet Elijah, Daniel H.
Samengo, Inés
Montemurro, Marcelo A.
author_sort Elijah, Daniel H.
collection PubMed
description Thalamic neurons have been long assumed to fire in tonic mode during perceptive states, and in burst mode during sleep and unconsciousness. However, recent evidence suggests that bursts may also be relevant in the encoding of sensory information. Here, we explore the neural code of such thalamic bursts. In order to assess whether the burst code is generic or whether it depends on the detailed properties of each bursting neuron, we analyzed two neuron models incorporating different levels of biological detail. One of the models contained no information of the biophysical processes entailed in spike generation, and described neuron activity at a phenomenological level. The second model represented the evolution of the individual ionic conductances involved in spiking and bursting, and required a large number of parameters. We analyzed the models' input selectivity using reverse correlation methods and information theory. We found that n-spike bursts from both models transmit information by modulating their spike count in response to changes to instantaneous input features, such as slope, phase, amplitude, etc. The stimulus feature that is most efficiently encoded by bursts, however, need not coincide with one of such classical features. We therefore searched for the optimal feature among all those that could be expressed as a linear transformation of the time-dependent input current. We found that bursting neurons transmitted 6 times more information about such more general features. The relevant events in the stimulus were located in a time window spanning ~100 ms before and ~20 ms after burst onset. Most importantly, the neural code employed by the simple and the biologically realistic models was largely the same, implying that the simple thalamic neuron model contains the essential ingredients that account for the computational properties of the thalamic burst code. Thus, our results suggest the n-spike burst code is a general property of thalamic neurons.
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spelling pubmed-45851432015-10-05 Thalamic neuron models encode stimulus information by burst-size modulation Elijah, Daniel H. Samengo, Inés Montemurro, Marcelo A. Front Comput Neurosci Neuroscience Thalamic neurons have been long assumed to fire in tonic mode during perceptive states, and in burst mode during sleep and unconsciousness. However, recent evidence suggests that bursts may also be relevant in the encoding of sensory information. Here, we explore the neural code of such thalamic bursts. In order to assess whether the burst code is generic or whether it depends on the detailed properties of each bursting neuron, we analyzed two neuron models incorporating different levels of biological detail. One of the models contained no information of the biophysical processes entailed in spike generation, and described neuron activity at a phenomenological level. The second model represented the evolution of the individual ionic conductances involved in spiking and bursting, and required a large number of parameters. We analyzed the models' input selectivity using reverse correlation methods and information theory. We found that n-spike bursts from both models transmit information by modulating their spike count in response to changes to instantaneous input features, such as slope, phase, amplitude, etc. The stimulus feature that is most efficiently encoded by bursts, however, need not coincide with one of such classical features. We therefore searched for the optimal feature among all those that could be expressed as a linear transformation of the time-dependent input current. We found that bursting neurons transmitted 6 times more information about such more general features. The relevant events in the stimulus were located in a time window spanning ~100 ms before and ~20 ms after burst onset. Most importantly, the neural code employed by the simple and the biologically realistic models was largely the same, implying that the simple thalamic neuron model contains the essential ingredients that account for the computational properties of the thalamic burst code. Thus, our results suggest the n-spike burst code is a general property of thalamic neurons. Frontiers Media S.A. 2015-09-23 /pmc/articles/PMC4585143/ /pubmed/26441623 http://dx.doi.org/10.3389/fncom.2015.00113 Text en Copyright © 2015 Elijah, Samengo and Montemurro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Elijah, Daniel H.
Samengo, Inés
Montemurro, Marcelo A.
Thalamic neuron models encode stimulus information by burst-size modulation
title Thalamic neuron models encode stimulus information by burst-size modulation
title_full Thalamic neuron models encode stimulus information by burst-size modulation
title_fullStr Thalamic neuron models encode stimulus information by burst-size modulation
title_full_unstemmed Thalamic neuron models encode stimulus information by burst-size modulation
title_short Thalamic neuron models encode stimulus information by burst-size modulation
title_sort thalamic neuron models encode stimulus information by burst-size modulation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585143/
https://www.ncbi.nlm.nih.gov/pubmed/26441623
http://dx.doi.org/10.3389/fncom.2015.00113
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