Cargando…

Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals

Integrating motivational signals with cognition is critical for goal-directed activities. The mechanisms that link neural changes with motivated working memory continue to be understood. Here, we tested how externally cued and non-cued (internally represented) reward and loss impact spatial working...

Descripción completa

Detalles Bibliográficos
Autores principales: Cho, Youngsun T., Moujaes, Flora, Schleifer, Charles H., Starc, Martina, Ji, Jie Lisa, Santamauro, Nicole, Adkinson, Brendan, Kolobaric, Antonija, Flynn, Morgan, Krystal, John H., Murray, John D., Repovs, Grega, Anticevic, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264479/
https://www.ncbi.nlm.nih.gov/pubmed/35346841
http://dx.doi.org/10.1016/j.neuroimage.2022.119139
_version_ 1784742973440786432
author Cho, Youngsun T.
Moujaes, Flora
Schleifer, Charles H.
Starc, Martina
Ji, Jie Lisa
Santamauro, Nicole
Adkinson, Brendan
Kolobaric, Antonija
Flynn, Morgan
Krystal, John H.
Murray, John D.
Repovs, Grega
Anticevic, Alan
author_facet Cho, Youngsun T.
Moujaes, Flora
Schleifer, Charles H.
Starc, Martina
Ji, Jie Lisa
Santamauro, Nicole
Adkinson, Brendan
Kolobaric, Antonija
Flynn, Morgan
Krystal, John H.
Murray, John D.
Repovs, Grega
Anticevic, Alan
author_sort Cho, Youngsun T.
collection PubMed
description Integrating motivational signals with cognition is critical for goal-directed activities. The mechanisms that link neural changes with motivated working memory continue to be understood. Here, we tested how externally cued and non-cued (internally represented) reward and loss impact spatial working memory precision and neural circuits in human subjects using fMRI. We translated the classic delayed-response spatial working memory paradigm from non-human primate studies to take advantage of a continuous numeric measure of working memory precision, and the wealth of translational neuroscience yielded by these studies. Our results demonstrated that both cued and non-cued reward and loss improved spatial working memory precision. Visual association regions of the posterior prefrontal and parietal cortices, specifically the precentral sulcus (PCS) and intraparietal sulcus (IPS), had increased BOLD signal during incentivized spatial working memory. A subset of these regions had trial-by-trial increases in BOLD signal that were associated with better working memory precision, suggesting that these regions may be critical for linking neural signals with motivated working memory. In contrast, regions straddling executive networks, including areas in the dorsolateral prefrontal cortex, anterior parietal cortex and cerebellum displayed decreased BOLD signal during incentivized working memory. While reward and loss similarly impacted working memory processes, they dissociated during feedback when money won or avoided in loss was given based on working memory performance. During feedback, the trial-by-trial amount and valence of reward/loss received was dissociated amongst regions such as the ventral striatum, habenula and periaqueductal gray. Overall, this work suggests motivated spatial working memory is supported by complex sensory processes, and that the IPS and PCS in the posterior frontoparietal cortices may be key regions for integrating motivational signals with spatial working memory precision.
format Online
Article
Text
id pubmed-9264479
institution National Center for Biotechnology Information
language English
publishDate 2022
record_format MEDLINE/PubMed
spelling pubmed-92644792022-07-08 Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals Cho, Youngsun T. Moujaes, Flora Schleifer, Charles H. Starc, Martina Ji, Jie Lisa Santamauro, Nicole Adkinson, Brendan Kolobaric, Antonija Flynn, Morgan Krystal, John H. Murray, John D. Repovs, Grega Anticevic, Alan Neuroimage Article Integrating motivational signals with cognition is critical for goal-directed activities. The mechanisms that link neural changes with motivated working memory continue to be understood. Here, we tested how externally cued and non-cued (internally represented) reward and loss impact spatial working memory precision and neural circuits in human subjects using fMRI. We translated the classic delayed-response spatial working memory paradigm from non-human primate studies to take advantage of a continuous numeric measure of working memory precision, and the wealth of translational neuroscience yielded by these studies. Our results demonstrated that both cued and non-cued reward and loss improved spatial working memory precision. Visual association regions of the posterior prefrontal and parietal cortices, specifically the precentral sulcus (PCS) and intraparietal sulcus (IPS), had increased BOLD signal during incentivized spatial working memory. A subset of these regions had trial-by-trial increases in BOLD signal that were associated with better working memory precision, suggesting that these regions may be critical for linking neural signals with motivated working memory. In contrast, regions straddling executive networks, including areas in the dorsolateral prefrontal cortex, anterior parietal cortex and cerebellum displayed decreased BOLD signal during incentivized working memory. While reward and loss similarly impacted working memory processes, they dissociated during feedback when money won or avoided in loss was given based on working memory performance. During feedback, the trial-by-trial amount and valence of reward/loss received was dissociated amongst regions such as the ventral striatum, habenula and periaqueductal gray. Overall, this work suggests motivated spatial working memory is supported by complex sensory processes, and that the IPS and PCS in the posterior frontoparietal cortices may be key regions for integrating motivational signals with spatial working memory precision. 2022-07-01 2022-03-25 /pmc/articles/PMC9264479/ /pubmed/35346841 http://dx.doi.org/10.1016/j.neuroimage.2022.119139 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Cho, Youngsun T.
Moujaes, Flora
Schleifer, Charles H.
Starc, Martina
Ji, Jie Lisa
Santamauro, Nicole
Adkinson, Brendan
Kolobaric, Antonija
Flynn, Morgan
Krystal, John H.
Murray, John D.
Repovs, Grega
Anticevic, Alan
Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title_full Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title_fullStr Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title_full_unstemmed Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title_short Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
title_sort reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264479/
https://www.ncbi.nlm.nih.gov/pubmed/35346841
http://dx.doi.org/10.1016/j.neuroimage.2022.119139
work_keys_str_mv AT choyoungsunt rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT moujaesflora rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT schleifercharlesh rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT starcmartina rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT jijielisa rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT santamauronicole rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT adkinsonbrendan rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT kolobaricantonija rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT flynnmorgan rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT krystaljohnh rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT murrayjohnd rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT repovsgrega rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals
AT anticevicalan rewardandlossincentivesimprovespatialworkingmemorybyshapingtrialbytrialposteriorfrontoparietalsignals