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      The Neural Representation of Prospective Choice during Spatial Planning and Decisions

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          Abstract

          We are remarkably adept at inferring the consequences of our actions, yet the neuronal mechanisms that allow us to plan a sequence of novel choices remain unclear. We used functional magnetic resonance imaging (fMRI) to investigate how the human brain plans the shortest path to a goal in novel mazes with one (shallow maze) or two (deep maze) choice points. We observed two distinct anterior prefrontal responses to demanding choices at the second choice point: one in rostrodorsal medial prefrontal cortex (rd-mPFC)/superior frontal gyrus (SFG) that was also sensitive to (deactivated by) demanding initial choices and another in lateral frontopolar cortex (lFPC), which was only engaged by demanding choices at the second choice point. Furthermore, we identified hippocampal responses during planning that correlated with subsequent choice accuracy and response time, particularly in mazes affording sequential choices. Psychophysiological interaction (PPI) analyses showed that coupling between the hippocampus and rd-mPFC increases during sequential (deep versus shallow) planning and is higher before correct versus incorrect choices. In short, using a naturalistic spatial planning paradigm, we reveal how the human brain represents sequential choices during planning without extensive training. Our data highlight a network centred on the cortical midline and hippocampus that allows us to make prospective choices while maintaining initial choices during planning in novel environments.

          Abstract

          Using neuroimaging and computational modelling, this study explains how the human brain represents initial versus subsequent choices during spatial planning in novel environments.

          Author Summary

          We are remarkably adept at inferring the consequences of our actions, even in novel situations. However, the neuronal mechanisms that allow us to plan a sequence of novel choices remain a mystery. One hypothesis is that anterior prefrontal brain regions can jump ahead from an initial decision to evaluate subsequent choices. Here, we examine how the brain represents initial versus subsequent choices of varying difficulty during spatial planning in novel environments. Specifically, participants visually searched for the shortest path to a goal in pictures of novel mazes that contained one or two path junctions. We monitored the participants’ brain activity during the task with functional magnetic resonance imaging (fMRI). We observed, in the anterior prefrontal brain, two distinct responses to demanding choices at the second junction: one in the rostrodorsal medial prefrontal cortex (rd-mPFC), which also signalled less demanding initial choices, and another one in the lateral frontopolar cortex (lFPC), which was only engaged by demanding choices at the second junction. Notably, interactions of the rd-mPFC with the hippocampus, a region associated with memory, increased when planning required extensive deliberation and particularly when planning led to accurate choices. Our findings show how humans can rapidly formulate a plan in novel environments. More broadly, these data uncover potential neural mechanisms underlying how we make inferences about states beyond a current subjective state.

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          Most cited references56

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          Preplay of future place cell sequences by hippocampal cellular assemblies.

          During spatial exploration, hippocampal neurons show a sequential firing pattern in which individual neurons fire specifically at particular locations along the animal's trajectory (place cells). According to the dominant model of hippocampal cell assembly activity, place cell firing order is established for the first time during exploration, to encode the spatial experience, and is subsequently replayed during rest or slow-wave sleep for consolidation of the encoded experience. Here we report that temporal sequences of firing of place cells expressed during a novel spatial experience occurred on a significant number of occasions during the resting or sleeping period preceding the experience. This phenomenon, which is called preplay, occurred in disjunction with sequences of replay of a familiar experience. These results suggest that internal neuronal dynamics during resting or sleep organize hippocampal cellular assemblies into temporal sequences that contribute to the encoding of a related novel experience occurring in the future.
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            Reactivation of hippocampal ensemble memories during sleep.

            Simultaneous recordings were made from large ensembles of hippocampal "place cells" in three rats during spatial behavioral tasks and in slow-wave sleep preceding and following these behaviors. Cells that fired together when the animal occupied particular locations in the environment exhibited an increased tendency to fire together during subsequent sleep, in comparison to sleep episodes preceding the behavioral tasks. Cells that were inactive during behavior, or that were active but had non-overlapping spatial firing, did not show this increase. This effect, which declined gradually during each post-behavior sleep session, may result from synaptic modification during waking experience. Information acquired during active behavior is thus re-expressed in hippocampal circuits during sleep, as postulated by some theories of memory consolidation.
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              Replay and time compression of recurring spike sequences in the hippocampus.

              Information in neuronal networks may be represented by the spatiotemporal patterns of spikes. Here we examined the temporal coordination of pyramidal cell spikes in the rat hippocampus during slow-wave sleep. In addition, rats were trained to run in a defined position in space (running wheel) to activate a selected group of pyramidal cells. A template-matching method and a joint probability map method were used for sequence search. Repeating spike sequences in excess of chance occurrence were examined by comparing the number of repeating sequences in the original spike trains and in surrogate trains after Monte Carlo shuffling of the spikes. Four different shuffling procedures were used to control for the population dynamics of hippocampal neurons. Repeating spike sequences in the recorded cell assemblies were present in both the awake and sleeping animal in excess of what might be predicted by random variations. Spike sequences observed during wheel running were "replayed" at a faster timescale during single sharp-wave bursts of slow-wave sleep. We hypothesize that the endogenously expressed spike sequences during sleep reflect reactivation of the circuitry modified by previous experience. Reactivation of acquired sequences may serve to consolidate information.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Biol
                PLoS Biol
                plos
                plosbiol
                PLoS Biology
                Public Library of Science (San Francisco, CA USA )
                1544-9173
                1545-7885
                12 January 2017
                January 2017
                12 January 2017
                : 15
                : 1
                : e1002588
                Affiliations
                [1 ]Wellcome Trust Centre for Neuroimaging, UCL Institute of Neurology, University College London, London, United Kingdom
                [2 ]UCL Institute of Cognitive Neuroscience, University College London, London, United Kingdom
                [3 ]Clinical, Education and Health Psychology, University College London, London, United Kingdom
                [4 ]UCL Institute of Neurology, University College London, London, United Kingdom
                Oxford University, UNITED KINGDOM
                Author notes

                The authors have declared that no competing interests exist.

                • Conceptualization: RKa JK NB KJF.

                • Formal analysis: RKa.

                • Funding acquisition: RKa KJF.

                • Investigation: RKa RKo.

                • Project administration: RKa.

                • Resources: WDP KJF.

                • Supervision: RKa KJF.

                • Writing – original draft: RKa KJF.

                • Writing – review & editing: RKa JK RKo WDP NB KJF.

                Author information
                http://orcid.org/0000-0002-0269-3790
                Article
                PBIOLOGY-D-16-01127
                10.1371/journal.pbio.1002588
                5231323
                28081125
                85ad0813-98db-41d6-91fb-3fbb5e6c803d
                © 2017 Kaplan et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 13 July 2016
                : 14 December 2016
                Page count
                Figures: 5, Tables: 1, Pages: 26
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award ID: 101261/Z/13/Z
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/100004440, Wellcome Trust;
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award Recipient :
                Funded by: Wellcome Trust (GB)
                Award ID: Strategic Award Grant 091593/Z/10/Z
                The Wellcome Trust Centre for Neuroimaging is supported by core funding from the Wellcome Trust (Strategic Award Grant 091593/Z/10/Z). This research was supported by grants from Medical Research Council to NB, separate grants from the Wellcome Trust to KJF and NB, and a Sir Henry Wellcome Fellowship (101261/Z/13/Z) to RKa. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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                fMRI data and accompanying statistical images are available from the UCL Institutional Data Access/Ethics Committee for researchers who meet the criteria for access to confidential data. To make a request, please contact Ms. Selina Mir by email at s.mir@ 123456uclb.com . Quantitative data for the X-Y and bar plots shown in Figs 2, 3, 4 and 5 are in the Supporting Information.

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