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The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice

Behavioural flexibility is an essential survival skill, yet our understanding of its neuronal substrates is still limited. While mouse research offers unique tools to dissect the neuronal circuits involved, the measurement of flexible behaviour in mice often suffers from long training times, poor ex...

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Autores principales: Havenith, Martha N., Zijderveld, Peter M., van Heukelum, Sabrina, Abghari, Shaghayegh, Tiesinga, Paul, Glennon, Jeffrey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423024/
https://www.ncbi.nlm.nih.gov/pubmed/30886236
http://dx.doi.org/10.1038/s41598-019-41250-w
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author Havenith, Martha N.
Zijderveld, Peter M.
van Heukelum, Sabrina
Abghari, Shaghayegh
Tiesinga, Paul
Glennon, Jeffrey C.
author_facet Havenith, Martha N.
Zijderveld, Peter M.
van Heukelum, Sabrina
Abghari, Shaghayegh
Tiesinga, Paul
Glennon, Jeffrey C.
author_sort Havenith, Martha N.
collection PubMed
description Behavioural flexibility is an essential survival skill, yet our understanding of its neuronal substrates is still limited. While mouse research offers unique tools to dissect the neuronal circuits involved, the measurement of flexible behaviour in mice often suffers from long training times, poor experimental control, and temporally imprecise binary (hit/miss) performance readouts. Here we present a virtual-environment task for mice that tackles these limitations. It offers fast training of vision-based rule reversals (~100 trials per reversal) with full stimulus control and continuous behavioural readouts. By generating multiple non-binary performance metrics per trial, it provides single-trial estimates not only of response accuracy and speed, but also of underlying processes like choice certainty and alertness (discussed in detail in a companion paper). Based on these metrics, we show that mice can predict new task rules long before they are able to execute them, and that this delay varies across animals. We also provide and validate single-trial estimates of whether an error was committed with or without awareness of the task rule. By tracking in unprecedented detail the cognitive dynamics underlying flexible behaviour, this task enables new investigations into the neuronal interactions that shape behavioural flexibility moment by moment.
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spelling pubmed-64230242019-03-26 The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice Havenith, Martha N. Zijderveld, Peter M. van Heukelum, Sabrina Abghari, Shaghayegh Tiesinga, Paul Glennon, Jeffrey C. Sci Rep Article Behavioural flexibility is an essential survival skill, yet our understanding of its neuronal substrates is still limited. While mouse research offers unique tools to dissect the neuronal circuits involved, the measurement of flexible behaviour in mice often suffers from long training times, poor experimental control, and temporally imprecise binary (hit/miss) performance readouts. Here we present a virtual-environment task for mice that tackles these limitations. It offers fast training of vision-based rule reversals (~100 trials per reversal) with full stimulus control and continuous behavioural readouts. By generating multiple non-binary performance metrics per trial, it provides single-trial estimates not only of response accuracy and speed, but also of underlying processes like choice certainty and alertness (discussed in detail in a companion paper). Based on these metrics, we show that mice can predict new task rules long before they are able to execute them, and that this delay varies across animals. We also provide and validate single-trial estimates of whether an error was committed with or without awareness of the task rule. By tracking in unprecedented detail the cognitive dynamics underlying flexible behaviour, this task enables new investigations into the neuronal interactions that shape behavioural flexibility moment by moment. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423024/ /pubmed/30886236 http://dx.doi.org/10.1038/s41598-019-41250-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Havenith, Martha N.
Zijderveld, Peter M.
van Heukelum, Sabrina
Abghari, Shaghayegh
Tiesinga, Paul
Glennon, Jeffrey C.
The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title_full The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title_fullStr The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title_full_unstemmed The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title_short The Virtual-Environment-Foraging Task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
title_sort virtual-environment-foraging task enables rapid training and single-trial metrics of rule acquisition and reversal in head-fixed mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423024/
https://www.ncbi.nlm.nih.gov/pubmed/30886236
http://dx.doi.org/10.1038/s41598-019-41250-w
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