Cargando…

Neuronal baseline shifts underlying boundary setting during free recall

Asked to freely recall items from a predefined set (e.g., animals), we rarely recall a wrong exemplar (e.g., a vegetable). This capability is so powerful and effortless that it is essentially taken for granted, yet, surprisingly, the underlying neuronal mechanisms are unknown. Here we investigate th...

Descripción completa

Detalles Bibliográficos
Autores principales: Norman, Yitzhak, Yeagle, Erin M., Harel, Michal, Mehta, Ashesh D., Malach, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670232/
https://www.ncbi.nlm.nih.gov/pubmed/29101322
http://dx.doi.org/10.1038/s41467-017-01184-1
_version_ 1783275981705838592
author Norman, Yitzhak
Yeagle, Erin M.
Harel, Michal
Mehta, Ashesh D.
Malach, Rafael
author_facet Norman, Yitzhak
Yeagle, Erin M.
Harel, Michal
Mehta, Ashesh D.
Malach, Rafael
author_sort Norman, Yitzhak
collection PubMed
description Asked to freely recall items from a predefined set (e.g., animals), we rarely recall a wrong exemplar (e.g., a vegetable). This capability is so powerful and effortless that it is essentially taken for granted, yet, surprisingly, the underlying neuronal mechanisms are unknown. Here we investigate this boundary setting mechanism using intracranial recordings (ECoG), in 12 patients undergoing epilepsy monitoring engaged in episodic free recall. After viewing vivid photographs from two categories (famous faces and places), patients were asked to freely recall these items, targeting each category in separate blocks. Our results reveal a rapid and sustained rise in neuronal activity (“baseline shift”) in high-order visual areas that persists throughout the free recall period and reflects the targeted category. We further show a more transient reactivation linked to individual recall events. The results point to baseline shift as a flexible top−down mechanism that biases spontaneous recall to remain within the required categorical boundaries.
format Online
Article
Text
id pubmed-5670232
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56702322017-11-07 Neuronal baseline shifts underlying boundary setting during free recall Norman, Yitzhak Yeagle, Erin M. Harel, Michal Mehta, Ashesh D. Malach, Rafael Nat Commun Article Asked to freely recall items from a predefined set (e.g., animals), we rarely recall a wrong exemplar (e.g., a vegetable). This capability is so powerful and effortless that it is essentially taken for granted, yet, surprisingly, the underlying neuronal mechanisms are unknown. Here we investigate this boundary setting mechanism using intracranial recordings (ECoG), in 12 patients undergoing epilepsy monitoring engaged in episodic free recall. After viewing vivid photographs from two categories (famous faces and places), patients were asked to freely recall these items, targeting each category in separate blocks. Our results reveal a rapid and sustained rise in neuronal activity (“baseline shift”) in high-order visual areas that persists throughout the free recall period and reflects the targeted category. We further show a more transient reactivation linked to individual recall events. The results point to baseline shift as a flexible top−down mechanism that biases spontaneous recall to remain within the required categorical boundaries. Nature Publishing Group UK 2017-11-03 /pmc/articles/PMC5670232/ /pubmed/29101322 http://dx.doi.org/10.1038/s41467-017-01184-1 Text en © The Author(s) 2017 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/.
spellingShingle Article
Norman, Yitzhak
Yeagle, Erin M.
Harel, Michal
Mehta, Ashesh D.
Malach, Rafael
Neuronal baseline shifts underlying boundary setting during free recall
title Neuronal baseline shifts underlying boundary setting during free recall
title_full Neuronal baseline shifts underlying boundary setting during free recall
title_fullStr Neuronal baseline shifts underlying boundary setting during free recall
title_full_unstemmed Neuronal baseline shifts underlying boundary setting during free recall
title_short Neuronal baseline shifts underlying boundary setting during free recall
title_sort neuronal baseline shifts underlying boundary setting during free recall
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670232/
https://www.ncbi.nlm.nih.gov/pubmed/29101322
http://dx.doi.org/10.1038/s41467-017-01184-1
work_keys_str_mv AT normanyitzhak neuronalbaselineshiftsunderlyingboundarysettingduringfreerecall
AT yeagleerinm neuronalbaselineshiftsunderlyingboundarysettingduringfreerecall
AT harelmichal neuronalbaselineshiftsunderlyingboundarysettingduringfreerecall
AT mehtaasheshd neuronalbaselineshiftsunderlyingboundarysettingduringfreerecall
AT malachrafael neuronalbaselineshiftsunderlyingboundarysettingduringfreerecall