Cargando…
Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation
As rats learn to search for multiple sources of food or water in a complex environment, they generate increasingly efficient trajectories between reward sites. Such spatial navigation capacity involves the replay of hippocampal place-cells during awake states, generating small sequences of spatially...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668845/ https://www.ncbi.nlm.nih.gov/pubmed/31306421 http://dx.doi.org/10.1371/journal.pcbi.1006624 |
_version_ | 1783440277220884480 |
---|---|
author | Cazin, Nicolas Llofriu Alonso, Martin Scleidorovich Chiodi, Pablo Pelc, Tatiana Harland, Bruce Weitzenfeld, Alfredo Fellous, Jean-Marc Dominey, Peter Ford |
author_facet | Cazin, Nicolas Llofriu Alonso, Martin Scleidorovich Chiodi, Pablo Pelc, Tatiana Harland, Bruce Weitzenfeld, Alfredo Fellous, Jean-Marc Dominey, Peter Ford |
author_sort | Cazin, Nicolas |
collection | PubMed |
description | As rats learn to search for multiple sources of food or water in a complex environment, they generate increasingly efficient trajectories between reward sites. Such spatial navigation capacity involves the replay of hippocampal place-cells during awake states, generating small sequences of spatially related place-cell activity that we call “snippets”. These snippets occur primarily during sharp-wave-ripples (SWRs). Here we focus on the role of such replay events, as the animal is learning a traveling salesperson task (TSP) across multiple trials. We hypothesize that snippet replay generates synthetic data that can substantially expand and restructure the experience available and make learning more optimal. We developed a model of snippet generation that is modulated by reward, propagated in the forward and reverse directions. This implements a form of spatial credit assignment for reinforcement learning. We use a biologically motivated computational framework known as ‘reservoir computing’ to model prefrontal cortex (PFC) in sequence learning, in which large pools of prewired neural elements process information dynamically through reverberations. This PFC model consolidates snippets into larger spatial sequences that may be later recalled by subsets of the original sequences. Our simulation experiments provide neurophysiological explanations for two pertinent observations related to navigation. Reward modulation allows the system to reject non-optimal segments of experienced trajectories, and reverse replay allows the system to “learn” trajectories that it has not physically experienced, both of which significantly contribute to the TSP behavior. |
format | Online Article Text |
id | pubmed-6668845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66688452019-08-06 Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation Cazin, Nicolas Llofriu Alonso, Martin Scleidorovich Chiodi, Pablo Pelc, Tatiana Harland, Bruce Weitzenfeld, Alfredo Fellous, Jean-Marc Dominey, Peter Ford PLoS Comput Biol Research Article As rats learn to search for multiple sources of food or water in a complex environment, they generate increasingly efficient trajectories between reward sites. Such spatial navigation capacity involves the replay of hippocampal place-cells during awake states, generating small sequences of spatially related place-cell activity that we call “snippets”. These snippets occur primarily during sharp-wave-ripples (SWRs). Here we focus on the role of such replay events, as the animal is learning a traveling salesperson task (TSP) across multiple trials. We hypothesize that snippet replay generates synthetic data that can substantially expand and restructure the experience available and make learning more optimal. We developed a model of snippet generation that is modulated by reward, propagated in the forward and reverse directions. This implements a form of spatial credit assignment for reinforcement learning. We use a biologically motivated computational framework known as ‘reservoir computing’ to model prefrontal cortex (PFC) in sequence learning, in which large pools of prewired neural elements process information dynamically through reverberations. This PFC model consolidates snippets into larger spatial sequences that may be later recalled by subsets of the original sequences. Our simulation experiments provide neurophysiological explanations for two pertinent observations related to navigation. Reward modulation allows the system to reject non-optimal segments of experienced trajectories, and reverse replay allows the system to “learn” trajectories that it has not physically experienced, both of which significantly contribute to the TSP behavior. Public Library of Science 2019-07-15 /pmc/articles/PMC6668845/ /pubmed/31306421 http://dx.doi.org/10.1371/journal.pcbi.1006624 Text en © 2019 Cazin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Cazin, Nicolas Llofriu Alonso, Martin Scleidorovich Chiodi, Pablo Pelc, Tatiana Harland, Bruce Weitzenfeld, Alfredo Fellous, Jean-Marc Dominey, Peter Ford Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title | Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title_full | Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title_fullStr | Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title_full_unstemmed | Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title_short | Reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
title_sort | reservoir computing model of prefrontal cortex creates novel combinations of previous navigation sequences from hippocampal place-cell replay with spatial reward propagation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668845/ https://www.ncbi.nlm.nih.gov/pubmed/31306421 http://dx.doi.org/10.1371/journal.pcbi.1006624 |
work_keys_str_mv | AT cazinnicolas reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT llofriualonsomartin reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT scleidorovichchiodipablo reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT pelctatiana reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT harlandbruce reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT weitzenfeldalfredo reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT fellousjeanmarc reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation AT domineypeterford reservoircomputingmodelofprefrontalcortexcreatesnovelcombinationsofpreviousnavigationsequencesfromhippocampalplacecellreplaywithspatialrewardpropagation |