Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates

Sensory events, cognitive processing and motor actions correlate with transient changes in neuronal activity. In cortex, these transients form widespread spatiotemporal patterns with largely unknown statistical regularities. Here, we show that activity associated with behavioral events carry the sig...

Full description

Bibliographic Details
Main Authors: Shan Yu, Tiago L Ribeiro, Christian Meisel, Samantha Chou, Andrew Mitz, Richard Saunders, Dietmar Plenz
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2017-11-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/27119
_version_ 1828222086789726208
author Shan Yu
Tiago L Ribeiro
Christian Meisel
Samantha Chou
Andrew Mitz
Richard Saunders
Dietmar Plenz
author_facet Shan Yu
Tiago L Ribeiro
Christian Meisel
Samantha Chou
Andrew Mitz
Richard Saunders
Dietmar Plenz
author_sort Shan Yu
collection DOAJ
description Sensory events, cognitive processing and motor actions correlate with transient changes in neuronal activity. In cortex, these transients form widespread spatiotemporal patterns with largely unknown statistical regularities. Here, we show that activity associated with behavioral events carry the signature of scale-invariant spatiotemporal clusters, neuronal avalanches. Using high-density microelectrode arrays in nonhuman primates, we recorded extracellular unit activity and the local field potential (LFP) in premotor and prefrontal cortex during motor and cognitive tasks. Unit activity and negative LFP deflections (nLFP) consistently changed in rate at single electrodes during tasks. Accordingly, nLFP clusters on the array deviated from scale-invariance compared to ongoing activity. Scale-invariance was recovered using ‘adaptive binning’, that is identifying clusters at temporal resolution given by task-induced changes in nLFP rate. Measures of LFP synchronization confirmed and computer simulations detailed our findings. We suggest optimization principles identified for avalanches during ongoing activity to apply to cortical information processing during behavior.
first_indexed 2024-04-12T16:49:23Z
format Article
id doaj.art-f0c06709a9e4442cbc1dad6c4f4ecc4f
institution Directory Open Access Journal
issn 2050-084X
language English
last_indexed 2024-04-12T16:49:23Z
publishDate 2017-11-01
publisher eLife Sciences Publications Ltd
record_format Article
series eLife
spelling doaj.art-f0c06709a9e4442cbc1dad6c4f4ecc4f2022-12-22T03:24:27ZengeLife Sciences Publications LtdeLife2050-084X2017-11-01610.7554/eLife.27119Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primatesShan Yu0https://orcid.org/0000-0002-9008-6658Tiago L Ribeiro1https://orcid.org/0000-0003-3195-9284Christian Meisel2Samantha Chou3Andrew Mitz4https://orcid.org/0000-0002-8045-0970Richard Saunders5Dietmar Plenz6https://orcid.org/0000-0002-0008-3657Section on Critical Brain Dynamics, National Institute of Mental Health, Bethesda, United StatesSection on Critical Brain Dynamics, National Institute of Mental Health, Bethesda, United StatesSection on Critical Brain Dynamics, National Institute of Mental Health, Bethesda, United StatesSection on Critical Brain Dynamics, National Institute of Mental Health, Bethesda, United StatesLaboratory of Neuropsychology, National Institute of Mental Health, Bethesda, United StatesLaboratory of Neuropsychology, National Institute of Mental Health, Bethesda, United StatesSection on Critical Brain Dynamics, National Institute of Mental Health, Bethesda, United StatesSensory events, cognitive processing and motor actions correlate with transient changes in neuronal activity. In cortex, these transients form widespread spatiotemporal patterns with largely unknown statistical regularities. Here, we show that activity associated with behavioral events carry the signature of scale-invariant spatiotemporal clusters, neuronal avalanches. Using high-density microelectrode arrays in nonhuman primates, we recorded extracellular unit activity and the local field potential (LFP) in premotor and prefrontal cortex during motor and cognitive tasks. Unit activity and negative LFP deflections (nLFP) consistently changed in rate at single electrodes during tasks. Accordingly, nLFP clusters on the array deviated from scale-invariance compared to ongoing activity. Scale-invariance was recovered using ‘adaptive binning’, that is identifying clusters at temporal resolution given by task-induced changes in nLFP rate. Measures of LFP synchronization confirmed and computer simulations detailed our findings. We suggest optimization principles identified for avalanches during ongoing activity to apply to cortical information processing during behavior.https://elifesciences.org/articles/27119cortexprefrontalpremotorbehaviorneuronal avalancheslocal-field potential
spellingShingle Shan Yu
Tiago L Ribeiro
Christian Meisel
Samantha Chou
Andrew Mitz
Richard Saunders
Dietmar Plenz
Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
eLife
cortex
prefrontal
premotor
behavior
neuronal avalanches
local-field potential
title Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
title_full Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
title_fullStr Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
title_full_unstemmed Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
title_short Maintained avalanche dynamics during task-induced changes of neuronal activity in nonhuman primates
title_sort maintained avalanche dynamics during task induced changes of neuronal activity in nonhuman primates
topic cortex
prefrontal
premotor
behavior
neuronal avalanches
local-field potential
url https://elifesciences.org/articles/27119
work_keys_str_mv AT shanyu maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT tiagolribeiro maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT christianmeisel maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT samanthachou maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT andrewmitz maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT richardsaunders maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates
AT dietmarplenz maintainedavalanchedynamicsduringtaskinducedchangesofneuronalactivityinnonhumanprimates