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Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales

Cortical activity is organized across multiple spatial and temporal scales. Most research on the dynamics of neuronal spiking is concerned with timescales of 1 ms–1 s, and little is known about spiking dynamics on timescales of tens of seconds and minutes. Here, we used frequency domain analyses to...

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Autores principales: Okun, Michael, Steinmetz, Nicholas A, Lak, Armin, Dervinis, Martynas, Harris, Kenneth D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458908/
https://www.ncbi.nlm.nih.gov/pubmed/30796825
http://dx.doi.org/10.1093/cercor/bhz023
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author Okun, Michael
Steinmetz, Nicholas A
Lak, Armin
Dervinis, Martynas
Harris, Kenneth D
author_facet Okun, Michael
Steinmetz, Nicholas A
Lak, Armin
Dervinis, Martynas
Harris, Kenneth D
author_sort Okun, Michael
collection PubMed
description Cortical activity is organized across multiple spatial and temporal scales. Most research on the dynamics of neuronal spiking is concerned with timescales of 1 ms–1 s, and little is known about spiking dynamics on timescales of tens of seconds and minutes. Here, we used frequency domain analyses to study the structure of individual neurons’ spiking activity and its coupling to local population rate and to arousal level across 0.01–100 Hz frequency range. In mouse medial prefrontal cortex, the spiking dynamics of individual neurons could be quantitatively captured by a combination of interspike interval and firing rate power spectrum distributions. The relative strength of coherence with local population often differed across timescales: a neuron strongly coupled to population rate on fast timescales could be weakly coupled on slow timescales, and vice versa. On slow but not fast timescales, a substantial proportion of neurons showed firing anticorrelated with the population. Infraslow firing rate changes were largely determined by arousal rather than by local factors, which could explain the timescale dependence of individual neurons’ population coupling strength. These observations demonstrate how neurons simultaneously partake in fast local dynamics, and slow brain-wide dynamics, extending our understanding of infraslow cortical activity beyond the mesoscale resolution of fMRI.
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spelling pubmed-64589082019-04-17 Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales Okun, Michael Steinmetz, Nicholas A Lak, Armin Dervinis, Martynas Harris, Kenneth D Cereb Cortex Original Articles Cortical activity is organized across multiple spatial and temporal scales. Most research on the dynamics of neuronal spiking is concerned with timescales of 1 ms–1 s, and little is known about spiking dynamics on timescales of tens of seconds and minutes. Here, we used frequency domain analyses to study the structure of individual neurons’ spiking activity and its coupling to local population rate and to arousal level across 0.01–100 Hz frequency range. In mouse medial prefrontal cortex, the spiking dynamics of individual neurons could be quantitatively captured by a combination of interspike interval and firing rate power spectrum distributions. The relative strength of coherence with local population often differed across timescales: a neuron strongly coupled to population rate on fast timescales could be weakly coupled on slow timescales, and vice versa. On slow but not fast timescales, a substantial proportion of neurons showed firing anticorrelated with the population. Infraslow firing rate changes were largely determined by arousal rather than by local factors, which could explain the timescale dependence of individual neurons’ population coupling strength. These observations demonstrate how neurons simultaneously partake in fast local dynamics, and slow brain-wide dynamics, extending our understanding of infraslow cortical activity beyond the mesoscale resolution of fMRI. Oxford University Press 2019-05 2019-02-23 /pmc/articles/PMC6458908/ /pubmed/30796825 http://dx.doi.org/10.1093/cercor/bhz023 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Okun, Michael
Steinmetz, Nicholas A
Lak, Armin
Dervinis, Martynas
Harris, Kenneth D
Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title_full Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title_fullStr Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title_full_unstemmed Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title_short Distinct Structure of Cortical Population Activity on Fast and Infraslow Timescales
title_sort distinct structure of cortical population activity on fast and infraslow timescales
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6458908/
https://www.ncbi.nlm.nih.gov/pubmed/30796825
http://dx.doi.org/10.1093/cercor/bhz023
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