Thalamic neuron models encode stimulus information by burst-size modulation

Autores
Elijah, Daniel H.; Samengo, Ines; Montemurro, Marcelo Alejandro
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
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.
Fil: Elijah, Daniel H.. University of Manchester; Reino Unido
Fil: Samengo, Ines. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Area de Investigación y Aplicaciones No Nucleares. Gerencia de Física (Centro Atómico Bariloche); Argentina
Fil: Montemurro, Marcelo Alejandro. University of Manchester; Reino Unido
Materia
BURST
INFORMATION THEORY
MULTIVARIATE ANALYSIS
NEURAL CODE
REVERSE CORRELATION
SINGLE NEURON MODEL
SPIKE-TRIGGERED AVERAGE
THALAMUS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/54961

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network_name_str CONICET Digital (CONICET)
spelling Thalamic neuron models encode stimulus information by burst-size modulationElijah, Daniel H.Samengo, InesMontemurro, Marcelo AlejandroBURSTINFORMATION THEORYMULTIVARIATE ANALYSISNEURAL CODEREVERSE CORRELATIONSINGLE NEURON MODELSPIKE-TRIGGERED AVERAGETHALAMUShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Thalamic 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.Fil: Elijah, Daniel H.. University of Manchester; Reino UnidoFil: Samengo, Ines. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Area de Investigación y Aplicaciones No Nucleares. Gerencia de Física (Centro Atómico Bariloche); ArgentinaFil: Montemurro, Marcelo Alejandro. University of Manchester; Reino UnidoFrontiers Research Foundation2015-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/54961Elijah, Daniel H.; Samengo, Ines; Montemurro, Marcelo Alejandro; Thalamic neuron models encode stimulus information by burst-size modulation; Frontiers Research Foundation; Frontiers in Computational Neuroscience; 9; SEP; 9-2015; 1-161662-5188CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.3389/fncom.2015.00113info:eu-repo/semantics/altIdentifier/url/https://www.frontiersin.org/articles/10.3389/fncom.2015.00113/fullinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:03:06Zoai:ri.conicet.gov.ar:11336/54961instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:03:07.324CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Thalamic neuron models encode stimulus information by burst-size modulation
title Thalamic neuron models encode stimulus information by burst-size modulation
spellingShingle Thalamic neuron models encode stimulus information by burst-size modulation
Elijah, Daniel H.
BURST
INFORMATION THEORY
MULTIVARIATE ANALYSIS
NEURAL CODE
REVERSE CORRELATION
SINGLE NEURON MODEL
SPIKE-TRIGGERED AVERAGE
THALAMUS
title_short 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_sort Thalamic neuron models encode stimulus information by burst-size modulation
dc.creator.none.fl_str_mv Elijah, Daniel H.
Samengo, Ines
Montemurro, Marcelo Alejandro
author Elijah, Daniel H.
author_facet Elijah, Daniel H.
Samengo, Ines
Montemurro, Marcelo Alejandro
author_role author
author2 Samengo, Ines
Montemurro, Marcelo Alejandro
author2_role author
author
dc.subject.none.fl_str_mv BURST
INFORMATION THEORY
MULTIVARIATE ANALYSIS
NEURAL CODE
REVERSE CORRELATION
SINGLE NEURON MODEL
SPIKE-TRIGGERED AVERAGE
THALAMUS
topic BURST
INFORMATION THEORY
MULTIVARIATE ANALYSIS
NEURAL CODE
REVERSE CORRELATION
SINGLE NEURON MODEL
SPIKE-TRIGGERED AVERAGE
THALAMUS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv 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.
Fil: Elijah, Daniel H.. University of Manchester; Reino Unido
Fil: Samengo, Ines. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Comisión Nacional de Energía Atómica. Gerencia del Area de Investigación y Aplicaciones No Nucleares. Gerencia de Física (Centro Atómico Bariloche); Argentina
Fil: Montemurro, Marcelo Alejandro. University of Manchester; Reino Unido
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.
publishDate 2015
dc.date.none.fl_str_mv 2015-09
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/54961
Elijah, Daniel H.; Samengo, Ines; Montemurro, Marcelo Alejandro; Thalamic neuron models encode stimulus information by burst-size modulation; Frontiers Research Foundation; Frontiers in Computational Neuroscience; 9; SEP; 9-2015; 1-16
1662-5188
CONICET Digital
CONICET
url http://hdl.handle.net/11336/54961
identifier_str_mv Elijah, Daniel H.; Samengo, Ines; Montemurro, Marcelo Alejandro; Thalamic neuron models encode stimulus information by burst-size modulation; Frontiers Research Foundation; Frontiers in Computational Neuroscience; 9; SEP; 9-2015; 1-16
1662-5188
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.3389/fncom.2015.00113
info:eu-repo/semantics/altIdentifier/url/https://www.frontiersin.org/articles/10.3389/fncom.2015.00113/full
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Frontiers Research Foundation
publisher.none.fl_str_mv Frontiers Research Foundation
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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