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Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory

Persistent neuronal spiking has long been considered the mechanism underlying working memory, but recent proposals argue for alternative, “activity-silent” substrates. Using monkey and human electrophysiology, we show here that attractor dynamics that control neural spiking during mnemonic periods i...

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Autores principales: Barbosa, Joao, Stein, Heike, Martinez, Rebecca L., Galan-Gadea, Adrià, Li, Sihai, Dalmau, Josep, Adam, Kirsten C.S., Valls-Solé, Josep, Constantinidis, Christos, Compte, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392810/
https://www.ncbi.nlm.nih.gov/pubmed/32572236
http://dx.doi.org/10.1038/s41593-020-0644-4
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author Barbosa, Joao
Stein, Heike
Martinez, Rebecca L.
Galan-Gadea, Adrià
Li, Sihai
Dalmau, Josep
Adam, Kirsten C.S.
Valls-Solé, Josep
Constantinidis, Christos
Compte, Albert
author_facet Barbosa, Joao
Stein, Heike
Martinez, Rebecca L.
Galan-Gadea, Adrià
Li, Sihai
Dalmau, Josep
Adam, Kirsten C.S.
Valls-Solé, Josep
Constantinidis, Christos
Compte, Albert
author_sort Barbosa, Joao
collection PubMed
description Persistent neuronal spiking has long been considered the mechanism underlying working memory, but recent proposals argue for alternative, “activity-silent” substrates. Using monkey and human electrophysiology, we show here that attractor dynamics that control neural spiking during mnemonic periods interact with activity-silent mechanisms in PFC. This interaction allows memory reactivations, which enhance serial biases in spatial working memory. Stimulus information was not decodable between trials, but remained present in activity-silent traces inferred from spiking synchrony in PFC. Just prior to the new stimulus, this latent trace was reignited into activity that recapitulated the previous stimulus representation. Importantly, the reactivation strength correlated with the strength of serial biases in both monkeys and humans, as predicted by a computational model integrating activity-based and activity-silent mechanisms. Finally, single-pulse TMS applied to the human prefrontal cortex between successive trials enhanced serial biases, demonstrating the causal role of prefrontal reactivations in determining working memory behavior.
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spelling pubmed-73928102020-12-22 Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory Barbosa, Joao Stein, Heike Martinez, Rebecca L. Galan-Gadea, Adrià Li, Sihai Dalmau, Josep Adam, Kirsten C.S. Valls-Solé, Josep Constantinidis, Christos Compte, Albert Nat Neurosci Article Persistent neuronal spiking has long been considered the mechanism underlying working memory, but recent proposals argue for alternative, “activity-silent” substrates. Using monkey and human electrophysiology, we show here that attractor dynamics that control neural spiking during mnemonic periods interact with activity-silent mechanisms in PFC. This interaction allows memory reactivations, which enhance serial biases in spatial working memory. Stimulus information was not decodable between trials, but remained present in activity-silent traces inferred from spiking synchrony in PFC. Just prior to the new stimulus, this latent trace was reignited into activity that recapitulated the previous stimulus representation. Importantly, the reactivation strength correlated with the strength of serial biases in both monkeys and humans, as predicted by a computational model integrating activity-based and activity-silent mechanisms. Finally, single-pulse TMS applied to the human prefrontal cortex between successive trials enhanced serial biases, demonstrating the causal role of prefrontal reactivations in determining working memory behavior. 2020-06-22 2020-08 /pmc/articles/PMC7392810/ /pubmed/32572236 http://dx.doi.org/10.1038/s41593-020-0644-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Barbosa, Joao
Stein, Heike
Martinez, Rebecca L.
Galan-Gadea, Adrià
Li, Sihai
Dalmau, Josep
Adam, Kirsten C.S.
Valls-Solé, Josep
Constantinidis, Christos
Compte, Albert
Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title_full Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title_fullStr Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title_full_unstemmed Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title_short Interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
title_sort interplay between persistent activity and activity-silent dynamics in prefrontal cortex underlies serial biases in working memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392810/
https://www.ncbi.nlm.nih.gov/pubmed/32572236
http://dx.doi.org/10.1038/s41593-020-0644-4
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