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BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice

Touchscreen technology is increasingly being used to characterize cognitive performance in rodent models of neuropsychiatric disorders. Researchers are attracted to the automated system and translational potential for touchscreen-based tasks. However, training time is extensive and some mouse strain...

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Autores principales: Turner, Karly M., Simpson, Christopher G., Burne, Thomas H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5281608/
https://www.ncbi.nlm.nih.gov/pubmed/28197083
http://dx.doi.org/10.3389/fnbeh.2017.00016
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author Turner, Karly M.
Simpson, Christopher G.
Burne, Thomas H. J.
author_facet Turner, Karly M.
Simpson, Christopher G.
Burne, Thomas H. J.
author_sort Turner, Karly M.
collection PubMed
description Touchscreen technology is increasingly being used to characterize cognitive performance in rodent models of neuropsychiatric disorders. Researchers are attracted to the automated system and translational potential for touchscreen-based tasks. However, training time is extensive and some mouse strains have struggled to learn touchscreen tasks. Here we compared the performance of commonly used C57BL/6 mice against the BALB/c mice, which are considered a poor performing strain, using a touchscreen task. BALB/c and C57BL/6 mice were trained to operate the touchscreens before learning a visual discrimination (VD) and reversal task. Following touchscreen testing, these strains were assessed for differences in locomotion and learned helplessness. BALB/c mice finished training in nearly half the number of sessions taken by C57BL/6 mice. Following training, mice learned a VD task where BALB/c mice again reached criteria in fewer than half the sessions required for C57BL/6 mice. Once acquired, there were no strain differences in % correct responses, correction trials or response latency. BALB/c mice also learnt the reversal task in significantly fewer sessions than C57BL/6 mice. On the open field test C57BL/6 mice traveled further and spent more time in the center, and spent less time immobile than BALB/c mice on the forced swim test (FST). After touchscreen testing, strains exhibited well-established behavioral traits demonstrating the extensive training and handling from touchscreen testing did not alter their behavioral phenotype. These results suggest that BALB/c mice can be examined using touchscreen tasks and that task adaptations may improve feasibility for researchers using different strains.
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spelling pubmed-52816082017-02-14 BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice Turner, Karly M. Simpson, Christopher G. Burne, Thomas H. J. Front Behav Neurosci Neuroscience Touchscreen technology is increasingly being used to characterize cognitive performance in rodent models of neuropsychiatric disorders. Researchers are attracted to the automated system and translational potential for touchscreen-based tasks. However, training time is extensive and some mouse strains have struggled to learn touchscreen tasks. Here we compared the performance of commonly used C57BL/6 mice against the BALB/c mice, which are considered a poor performing strain, using a touchscreen task. BALB/c and C57BL/6 mice were trained to operate the touchscreens before learning a visual discrimination (VD) and reversal task. Following touchscreen testing, these strains were assessed for differences in locomotion and learned helplessness. BALB/c mice finished training in nearly half the number of sessions taken by C57BL/6 mice. Following training, mice learned a VD task where BALB/c mice again reached criteria in fewer than half the sessions required for C57BL/6 mice. Once acquired, there were no strain differences in % correct responses, correction trials or response latency. BALB/c mice also learnt the reversal task in significantly fewer sessions than C57BL/6 mice. On the open field test C57BL/6 mice traveled further and spent more time in the center, and spent less time immobile than BALB/c mice on the forced swim test (FST). After touchscreen testing, strains exhibited well-established behavioral traits demonstrating the extensive training and handling from touchscreen testing did not alter their behavioral phenotype. These results suggest that BALB/c mice can be examined using touchscreen tasks and that task adaptations may improve feasibility for researchers using different strains. Frontiers Media S.A. 2017-01-31 /pmc/articles/PMC5281608/ /pubmed/28197083 http://dx.doi.org/10.3389/fnbeh.2017.00016 Text en Copyright © 2017 Turner, Simpson and Burne. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Turner, Karly M.
Simpson, Christopher G.
Burne, Thomas H. J.
BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title_full BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title_fullStr BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title_full_unstemmed BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title_short BALB/c Mice Can Learn Touchscreen Visual Discrimination and Reversal Tasks Faster than C57BL/6 Mice
title_sort balb/c mice can learn touchscreen visual discrimination and reversal tasks faster than c57bl/6 mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5281608/
https://www.ncbi.nlm.nih.gov/pubmed/28197083
http://dx.doi.org/10.3389/fnbeh.2017.00016
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