Cargando…

Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution

Local field potential (LFP) power in the gamma frequency is modulated by cognitive variables during task execution. We sought to examine whether such modulations only emerge when task rules are established. We therefore analyzed neuronal firing and LFPs in different prefrontal subdivisions before an...

Descripción completa

Detalles Bibliográficos
Autores principales: Singh, Balbir, Wang, Zhengyang, Constantinidis, Christos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175284/
https://www.ncbi.nlm.nih.gov/pubmed/37169826
http://dx.doi.org/10.1038/s42003-023-04855-6
_version_ 1785040183593271296
author Singh, Balbir
Wang, Zhengyang
Constantinidis, Christos
author_facet Singh, Balbir
Wang, Zhengyang
Constantinidis, Christos
author_sort Singh, Balbir
collection PubMed
description Local field potential (LFP) power in the gamma frequency is modulated by cognitive variables during task execution. We sought to examine whether such modulations only emerge when task rules are established. We therefore analyzed neuronal firing and LFPs in different prefrontal subdivisions before and after the same monkeys were trained to perform cognitive tasks. Prior to task rule learning, sites containing neurons selective for stimuli already exhibited increased gamma power during and after the passive viewing of stimuli compared to the baseline period. Unexpectedly, when the same monkeys learned to maintain these stimuli in working memory, the elevation of gamma power above the baseline was diminished, despite an overall increase in firing rate. Learning and executing the task further decoupled LFP power from single neuron firing. Gamma power decreased at the time when subjects needed to make a judgment about whether two stimuli were the same or not, and differential gamma power was observed for matching and nonmatching stimuli. Our results indicate that prefrontal gamma power emerges spontaneously, not necessarily tied to a cognitive task being executed.
format Online
Article
Text
id pubmed-10175284
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-101752842023-05-13 Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution Singh, Balbir Wang, Zhengyang Constantinidis, Christos Commun Biol Article Local field potential (LFP) power in the gamma frequency is modulated by cognitive variables during task execution. We sought to examine whether such modulations only emerge when task rules are established. We therefore analyzed neuronal firing and LFPs in different prefrontal subdivisions before and after the same monkeys were trained to perform cognitive tasks. Prior to task rule learning, sites containing neurons selective for stimuli already exhibited increased gamma power during and after the passive viewing of stimuli compared to the baseline period. Unexpectedly, when the same monkeys learned to maintain these stimuli in working memory, the elevation of gamma power above the baseline was diminished, despite an overall increase in firing rate. Learning and executing the task further decoupled LFP power from single neuron firing. Gamma power decreased at the time when subjects needed to make a judgment about whether two stimuli were the same or not, and differential gamma power was observed for matching and nonmatching stimuli. Our results indicate that prefrontal gamma power emerges spontaneously, not necessarily tied to a cognitive task being executed. Nature Publishing Group UK 2023-05-11 /pmc/articles/PMC10175284/ /pubmed/37169826 http://dx.doi.org/10.1038/s42003-023-04855-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Singh, Balbir
Wang, Zhengyang
Constantinidis, Christos
Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title_full Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title_fullStr Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title_full_unstemmed Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title_short Neuronal selectivity for stimulus information determines prefrontal LFP gamma power regardless of task execution
title_sort neuronal selectivity for stimulus information determines prefrontal lfp gamma power regardless of task execution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175284/
https://www.ncbi.nlm.nih.gov/pubmed/37169826
http://dx.doi.org/10.1038/s42003-023-04855-6
work_keys_str_mv AT singhbalbir neuronalselectivityforstimulusinformationdeterminesprefrontallfpgammapowerregardlessoftaskexecution
AT wangzhengyang neuronalselectivityforstimulusinformationdeterminesprefrontallfpgammapowerregardlessoftaskexecution
AT constantinidischristos neuronalselectivityforstimulusinformationdeterminesprefrontallfpgammapowerregardlessoftaskexecution