Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782440514379841536 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4928887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT roffmanjoshual dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT tanneralexandras dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT eryilmazhamdi dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT rodriguezthompsonanais dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT silversteinnoahj dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT honewfei dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT nitensonadamz dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT chondedanielb dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT grevedouglasn dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT abidarghamanissa dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT bucknerrandyl dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT manoachdaras dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT rosenbrucer dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT hookerjacobm dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory AT catanaciprian dopamined1signalingorganizesnetworkdynamicsunderlyingworkingmemory |