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Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation

Many neurological and psychiatric disorders are characterized by deficits in cognitive flexibility. Modeling cognitive flexibility in mice enables the investigation of mechanisms underlying these deficits. The majority of currently available behavioral tests targeting this cognitive domain are rever...

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Detalles Bibliográficos
Autores principales: Remmelink, Esther, Smit, August B., Verhage, Matthijs, Loos, Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066605/
https://www.ncbi.nlm.nih.gov/pubmed/27918287
http://dx.doi.org/10.1101/lm.042085.116
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author Remmelink, Esther
Smit, August B.
Verhage, Matthijs
Loos, Maarten
author_facet Remmelink, Esther
Smit, August B.
Verhage, Matthijs
Loos, Maarten
author_sort Remmelink, Esther
collection PubMed
description Many neurological and psychiatric disorders are characterized by deficits in cognitive flexibility. Modeling cognitive flexibility in mice enables the investigation of mechanisms underlying these deficits. The majority of currently available behavioral tests targeting this cognitive domain are reversal learning tasks that require scheduled food restriction, extended training periods and labor-intensive, and stress-inducing animal handling. Here, we describe a novel 4-day (4-d) continuously running task measuring discrimination- and reversal learning in an automated home cage (CognitionWall DL/RL task) that largely eliminates these limitations. In this task, mice can earn unlimited number of food rewards by passing through the correct hole of the three-holed CognitionWall. To assess the validity and sensitivity of this novel task, the performance of C57BL/6J mice, amyloid precursor protein/presenilin1 transgenic (APP/PS1) mice, α-calmodulin kinase-II (αCaMKII) T305D knock-in mice, and mice with an orbitofrontal cortex lesion were examined. We found that C57BL/6J mice reach stable performance levels within the 4 d of the task, while experiencing only slight reductions in weight and no major effects on circadian rhythm. The task detected learning deficits in APP/PS1 transgenic and αCaMKII T305D mutant mice. Additionally, we established that the orbitofrontal cortex underlies reversal learning performance in our task. Because of its short duration and the absence of food deprivation and concurrent weight loss, this novel automated home-cage task substantially improves comprehensive preclinical assessment of cognitive functions in mouse models of psychiatric and neurological disorders and also enables analysis during specific developmental stages.
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spelling pubmed-50666052016-11-01 Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation Remmelink, Esther Smit, August B. Verhage, Matthijs Loos, Maarten Learn Mem Research Many neurological and psychiatric disorders are characterized by deficits in cognitive flexibility. Modeling cognitive flexibility in mice enables the investigation of mechanisms underlying these deficits. The majority of currently available behavioral tests targeting this cognitive domain are reversal learning tasks that require scheduled food restriction, extended training periods and labor-intensive, and stress-inducing animal handling. Here, we describe a novel 4-day (4-d) continuously running task measuring discrimination- and reversal learning in an automated home cage (CognitionWall DL/RL task) that largely eliminates these limitations. In this task, mice can earn unlimited number of food rewards by passing through the correct hole of the three-holed CognitionWall. To assess the validity and sensitivity of this novel task, the performance of C57BL/6J mice, amyloid precursor protein/presenilin1 transgenic (APP/PS1) mice, α-calmodulin kinase-II (αCaMKII) T305D knock-in mice, and mice with an orbitofrontal cortex lesion were examined. We found that C57BL/6J mice reach stable performance levels within the 4 d of the task, while experiencing only slight reductions in weight and no major effects on circadian rhythm. The task detected learning deficits in APP/PS1 transgenic and αCaMKII T305D mutant mice. Additionally, we established that the orbitofrontal cortex underlies reversal learning performance in our task. Because of its short duration and the absence of food deprivation and concurrent weight loss, this novel automated home-cage task substantially improves comprehensive preclinical assessment of cognitive functions in mouse models of psychiatric and neurological disorders and also enables analysis during specific developmental stages. Cold Spring Harbor Laboratory Press 2016-11 /pmc/articles/PMC5066605/ /pubmed/27918287 http://dx.doi.org/10.1101/lm.042085.116 Text en © 2016 Remmelink et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Learning & Memory, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Remmelink, Esther
Smit, August B.
Verhage, Matthijs
Loos, Maarten
Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title_full Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title_fullStr Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title_full_unstemmed Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title_short Measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
title_sort measuring discrimination- and reversal learning in mouse models within 4 days and without prior food deprivation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066605/
https://www.ncbi.nlm.nih.gov/pubmed/27918287
http://dx.doi.org/10.1101/lm.042085.116
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