Cargando…

Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles

The most basic functional role commonly ascribed to synchrony in the brain is that of amplifying excitatory neuronal signals. The reasoning is straightforward: When positive charge is injected into a leaky target neuron over a time window of positive duration, some of it will have time to leak back...

Descripción completa

Detalles Bibliográficos
Autores principales: Börgers, Christoph, Li, Jie, Kopell, Nancy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916341/
https://www.ncbi.nlm.nih.gov/pubmed/27334376
http://dx.doi.org/10.1186/2190-8567-4-10
_version_ 1782438815833522176
author Börgers, Christoph
Li, Jie
Kopell, Nancy
author_facet Börgers, Christoph
Li, Jie
Kopell, Nancy
author_sort Börgers, Christoph
collection PubMed
description The most basic functional role commonly ascribed to synchrony in the brain is that of amplifying excitatory neuronal signals. The reasoning is straightforward: When positive charge is injected into a leaky target neuron over a time window of positive duration, some of it will have time to leak back out before an action potential is triggered in the target, and it will in that sense be wasted. If the goal is to elicit a firing response in the target using as little charge as possible, it seems best to deliver the charge all at once, i.e., in perfect synchrony. In this article, we show that this reasoning is correct only if one assumes that the input ceases when the target crosses the firing threshold, but before it actually fires. If the input ceases later—for instance, in response to a feedback signal triggered by the firing of the target—the “most economical” way of delivering input (the way that requires the least total amount of input) is no longer precisely synchronous, but merely approximately so. If the target is a heterogeneous network, as it always is in the brain, then ceasing the input “when the target crosses the firing threshold” is not an option, because there is no single moment when the firing threshold is crossed. In this sense, precise synchrony is never optimal in the brain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2190-8567-4-10) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4916341
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-49163412016-07-06 Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles Börgers, Christoph Li, Jie Kopell, Nancy J Math Neurosci Research The most basic functional role commonly ascribed to synchrony in the brain is that of amplifying excitatory neuronal signals. The reasoning is straightforward: When positive charge is injected into a leaky target neuron over a time window of positive duration, some of it will have time to leak back out before an action potential is triggered in the target, and it will in that sense be wasted. If the goal is to elicit a firing response in the target using as little charge as possible, it seems best to deliver the charge all at once, i.e., in perfect synchrony. In this article, we show that this reasoning is correct only if one assumes that the input ceases when the target crosses the firing threshold, but before it actually fires. If the input ceases later—for instance, in response to a feedback signal triggered by the firing of the target—the “most economical” way of delivering input (the way that requires the least total amount of input) is no longer precisely synchronous, but merely approximately so. If the target is a heterogeneous network, as it always is in the brain, then ceasing the input “when the target crosses the firing threshold” is not an option, because there is no single moment when the firing threshold is crossed. In this sense, precise synchrony is never optimal in the brain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2190-8567-4-10) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-04-25 /pmc/articles/PMC4916341/ /pubmed/27334376 http://dx.doi.org/10.1186/2190-8567-4-10 Text en © C. Börgers et al.; licensee Springer 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Börgers, Christoph
Li, Jie
Kopell, Nancy
Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title_full Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title_fullStr Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title_full_unstemmed Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title_short Approximate, not Perfect Synchrony Maximizes the Downstream Effectiveness of Excitatory Neuronal Ensembles
title_sort approximate, not perfect synchrony maximizes the downstream effectiveness of excitatory neuronal ensembles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916341/
https://www.ncbi.nlm.nih.gov/pubmed/27334376
http://dx.doi.org/10.1186/2190-8567-4-10
work_keys_str_mv AT borgerschristoph approximatenotperfectsynchronymaximizesthedownstreameffectivenessofexcitatoryneuronalensembles
AT lijie approximatenotperfectsynchronymaximizesthedownstreameffectivenessofexcitatoryneuronalensembles
AT kopellnancy approximatenotperfectsynchronymaximizesthedownstreameffectivenessofexcitatoryneuronalensembles