Cargando…

Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation

Humans and non-human animals show great flexibility in spatial navigation, including the ability to return to specific locations based on as few as one single experience. To study spatial navigation in the laboratory, watermaze tasks, in which rats have to find a hidden platform in a pool of cloudy...

Descripción completa

Detalles Bibliográficos
Autores principales: Tessereau, Charline, O’Dea, Reuben, Coombes, Stephen, Bast, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042550/
https://www.ncbi.nlm.nih.gov/pubmed/33954259
http://dx.doi.org/10.1177/2398212820975634
_version_ 1783678148309680128
author Tessereau, Charline
O’Dea, Reuben
Coombes, Stephen
Bast, Tobias
author_facet Tessereau, Charline
O’Dea, Reuben
Coombes, Stephen
Bast, Tobias
author_sort Tessereau, Charline
collection PubMed
description Humans and non-human animals show great flexibility in spatial navigation, including the ability to return to specific locations based on as few as one single experience. To study spatial navigation in the laboratory, watermaze tasks, in which rats have to find a hidden platform in a pool of cloudy water surrounded by spatial cues, have long been used. Analogous tasks have been developed for human participants using virtual environments. Spatial learning in the watermaze is facilitated by the hippocampus. In particular, rapid, one-trial, allocentric place learning, as measured in the delayed-matching-to-place variant of the watermaze task, which requires rodents to learn repeatedly new locations in a familiar environment, is hippocampal dependent. In this article, we review some computational principles, embedded within a reinforcement learning framework, that utilise hippocampal spatial representations for navigation in watermaze tasks. We consider which key elements underlie their efficacy, and discuss their limitations in accounting for hippocampus-dependent navigation, both in terms of behavioural performance (i.e. how well do they reproduce behavioural measures of rapid place learning) and neurobiological realism (i.e. how well do they map to neurobiological substrates involved in rapid place learning). We discuss how an actor–critic architecture, enabling simultaneous assessment of the value of the current location and of the optimal direction to follow, can reproduce one-trial place learning performance as shown on watermaze and virtual delayed-matching-to-place tasks by rats and humans, respectively, if complemented with map-like place representations. The contribution of actor–critic mechanisms to delayed-matching-to-place performance is consistent with neurobiological findings implicating the striatum and hippocampo-striatal interaction in delayed-matching-to-place performance, given that the striatum has been associated with actor–critic mechanisms. Moreover, we illustrate that hierarchical computations embedded within an actor–critic architecture may help to account for aspects of flexible spatial navigation. The hierarchical reinforcement learning approach separates trajectory control via a temporal-difference error from goal selection via a goal prediction error and may account for flexible, trial-specific, navigation to familiar goal locations, as required in some arm-maze place memory tasks, although it does not capture one-trial learning of new goal locations, as observed in open field, including watermaze and virtual, delayed-matching-to-place tasks. Future models of one-shot learning of new goal locations, as observed on delayed-matching-to-place tasks, should incorporate hippocampal plasticity mechanisms that integrate new goal information with allocentric place representation, as such mechanisms are supported by substantial empirical evidence.
format Online
Article
Text
id pubmed-8042550
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-80425502021-05-04 Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation Tessereau, Charline O’Dea, Reuben Coombes, Stephen Bast, Tobias Brain Neurosci Adv Research Paper (Special Collection: Within and beyond the medial temporal lobe: brain circuits and mechanisms of recognition and place memory) Humans and non-human animals show great flexibility in spatial navigation, including the ability to return to specific locations based on as few as one single experience. To study spatial navigation in the laboratory, watermaze tasks, in which rats have to find a hidden platform in a pool of cloudy water surrounded by spatial cues, have long been used. Analogous tasks have been developed for human participants using virtual environments. Spatial learning in the watermaze is facilitated by the hippocampus. In particular, rapid, one-trial, allocentric place learning, as measured in the delayed-matching-to-place variant of the watermaze task, which requires rodents to learn repeatedly new locations in a familiar environment, is hippocampal dependent. In this article, we review some computational principles, embedded within a reinforcement learning framework, that utilise hippocampal spatial representations for navigation in watermaze tasks. We consider which key elements underlie their efficacy, and discuss their limitations in accounting for hippocampus-dependent navigation, both in terms of behavioural performance (i.e. how well do they reproduce behavioural measures of rapid place learning) and neurobiological realism (i.e. how well do they map to neurobiological substrates involved in rapid place learning). We discuss how an actor–critic architecture, enabling simultaneous assessment of the value of the current location and of the optimal direction to follow, can reproduce one-trial place learning performance as shown on watermaze and virtual delayed-matching-to-place tasks by rats and humans, respectively, if complemented with map-like place representations. The contribution of actor–critic mechanisms to delayed-matching-to-place performance is consistent with neurobiological findings implicating the striatum and hippocampo-striatal interaction in delayed-matching-to-place performance, given that the striatum has been associated with actor–critic mechanisms. Moreover, we illustrate that hierarchical computations embedded within an actor–critic architecture may help to account for aspects of flexible spatial navigation. The hierarchical reinforcement learning approach separates trajectory control via a temporal-difference error from goal selection via a goal prediction error and may account for flexible, trial-specific, navigation to familiar goal locations, as required in some arm-maze place memory tasks, although it does not capture one-trial learning of new goal locations, as observed in open field, including watermaze and virtual, delayed-matching-to-place tasks. Future models of one-shot learning of new goal locations, as observed on delayed-matching-to-place tasks, should incorporate hippocampal plasticity mechanisms that integrate new goal information with allocentric place representation, as such mechanisms are supported by substantial empirical evidence. SAGE Publications 2021-04-09 /pmc/articles/PMC8042550/ /pubmed/33954259 http://dx.doi.org/10.1177/2398212820975634 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Paper (Special Collection: Within and beyond the medial temporal lobe: brain circuits and mechanisms of recognition and place memory)
Tessereau, Charline
O’Dea, Reuben
Coombes, Stephen
Bast, Tobias
Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title_full Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title_fullStr Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title_full_unstemmed Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title_short Reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
title_sort reinforcement learning approaches to hippocampus-dependent flexible spatial navigation
topic Research Paper (Special Collection: Within and beyond the medial temporal lobe: brain circuits and mechanisms of recognition and place memory)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042550/
https://www.ncbi.nlm.nih.gov/pubmed/33954259
http://dx.doi.org/10.1177/2398212820975634
work_keys_str_mv AT tessereaucharline reinforcementlearningapproachestohippocampusdependentflexiblespatialnavigation
AT odeareuben reinforcementlearningapproachestohippocampusdependentflexiblespatialnavigation
AT coombesstephen reinforcementlearningapproachestohippocampusdependentflexiblespatialnavigation
AT basttobias reinforcementlearningapproachestohippocampusdependentflexiblespatialnavigation