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...
Autores principales: | , , |
---|---|
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 |