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Dopamine D(1) signaling organizes network dynamics underlying working memory

Local prefrontal dopamine signaling supports working memory by tuning pyramidal neurons to task-relevant stimuli. Enabled by simultaneous positron emission tomography–magnetic resonance imaging (PET-MRI), we determined whether neuromodulatory effects of dopamine scale to the level of cortical networ...

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Autores principales: Roffman, Joshua L., Tanner, Alexandra S., Eryilmaz, Hamdi, Rodriguez-Thompson, Anais, Silverstein, Noah J., Ho, New Fei, Nitenson, Adam Z., Chonde, Daniel B., Greve, Douglas N., Abi-Dargham, Anissa, Buckner, Randy L., Manoach, Dara S., Rosen, Bruce R., Hooker, Jacob M., Catana, Ciprian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928887/
https://www.ncbi.nlm.nih.gov/pubmed/27386561
http://dx.doi.org/10.1126/sciadv.1501672
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author Roffman, Joshua L.
Tanner, Alexandra S.
Eryilmaz, Hamdi
Rodriguez-Thompson, Anais
Silverstein, Noah J.
Ho, New Fei
Nitenson, Adam Z.
Chonde, Daniel B.
Greve, Douglas N.
Abi-Dargham, Anissa
Buckner, Randy L.
Manoach, Dara S.
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
author_facet Roffman, Joshua L.
Tanner, Alexandra S.
Eryilmaz, Hamdi
Rodriguez-Thompson, Anais
Silverstein, Noah J.
Ho, New Fei
Nitenson, Adam Z.
Chonde, Daniel B.
Greve, Douglas N.
Abi-Dargham, Anissa
Buckner, Randy L.
Manoach, Dara S.
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
author_sort Roffman, Joshua L.
collection PubMed
description Local prefrontal dopamine signaling supports working memory by tuning pyramidal neurons to task-relevant stimuli. Enabled by simultaneous positron emission tomography–magnetic resonance imaging (PET-MRI), we determined whether neuromodulatory effects of dopamine scale to the level of cortical networks and coordinate their interplay during working memory. Among network territories, mean cortical D(1) receptor densities differed substantially but were strongly interrelated, suggesting cross-network regulation. Indeed, mean cortical D(1) density predicted working memory–emergent decoupling of the frontoparietal and default networks, which respectively manage task-related and internal stimuli. In contrast, striatal D(1) predicted opposing effects within these two networks but no between-network effects. These findings specifically link cortical dopamine signaling to network crosstalk that redirects cognitive resources to working memory, echoing neuromodulatory effects of D(1) signaling on the level of cortical microcircuits.
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spelling pubmed-49288872016-07-06 Dopamine D(1) signaling organizes network dynamics underlying working memory Roffman, Joshua L. Tanner, Alexandra S. Eryilmaz, Hamdi Rodriguez-Thompson, Anais Silverstein, Noah J. Ho, New Fei Nitenson, Adam Z. Chonde, Daniel B. Greve, Douglas N. Abi-Dargham, Anissa Buckner, Randy L. Manoach, Dara S. Rosen, Bruce R. Hooker, Jacob M. Catana, Ciprian Sci Adv Research Articles Local prefrontal dopamine signaling supports working memory by tuning pyramidal neurons to task-relevant stimuli. Enabled by simultaneous positron emission tomography–magnetic resonance imaging (PET-MRI), we determined whether neuromodulatory effects of dopamine scale to the level of cortical networks and coordinate their interplay during working memory. Among network territories, mean cortical D(1) receptor densities differed substantially but were strongly interrelated, suggesting cross-network regulation. Indeed, mean cortical D(1) density predicted working memory–emergent decoupling of the frontoparietal and default networks, which respectively manage task-related and internal stimuli. In contrast, striatal D(1) predicted opposing effects within these two networks but no between-network effects. These findings specifically link cortical dopamine signaling to network crosstalk that redirects cognitive resources to working memory, echoing neuromodulatory effects of D(1) signaling on the level of cortical microcircuits. American Association for the Advancement of Science 2016-06-03 /pmc/articles/PMC4928887/ /pubmed/27386561 http://dx.doi.org/10.1126/sciadv.1501672 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Roffman, Joshua L.
Tanner, Alexandra S.
Eryilmaz, Hamdi
Rodriguez-Thompson, Anais
Silverstein, Noah J.
Ho, New Fei
Nitenson, Adam Z.
Chonde, Daniel B.
Greve, Douglas N.
Abi-Dargham, Anissa
Buckner, Randy L.
Manoach, Dara S.
Rosen, Bruce R.
Hooker, Jacob M.
Catana, Ciprian
Dopamine D(1) signaling organizes network dynamics underlying working memory
title Dopamine D(1) signaling organizes network dynamics underlying working memory
title_full Dopamine D(1) signaling organizes network dynamics underlying working memory
title_fullStr Dopamine D(1) signaling organizes network dynamics underlying working memory
title_full_unstemmed Dopamine D(1) signaling organizes network dynamics underlying working memory
title_short Dopamine D(1) signaling organizes network dynamics underlying working memory
title_sort dopamine d(1) signaling organizes network dynamics underlying working memory
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928887/
https://www.ncbi.nlm.nih.gov/pubmed/27386561
http://dx.doi.org/10.1126/sciadv.1501672
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