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A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice

Cognitive flexibility refers to various processes which enable behaviors to be modified on the basis of a change in the contingencies between stimuli or responses and their associated outcomes. Reversal learning is a form of cognitive flexibility which measures the ability to adjust responding based...

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Autores principales: Piantadosi, Patrick T., Lieberman, Abby G., Pickens, Charles L., Bergstrom, Hadley C., Holmes, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298539/
https://www.ncbi.nlm.nih.gov/pubmed/30559117
http://dx.doi.org/10.1101/lm.048264.118
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author Piantadosi, Patrick T.
Lieberman, Abby G.
Pickens, Charles L.
Bergstrom, Hadley C.
Holmes, Andrew
author_facet Piantadosi, Patrick T.
Lieberman, Abby G.
Pickens, Charles L.
Bergstrom, Hadley C.
Holmes, Andrew
author_sort Piantadosi, Patrick T.
collection PubMed
description Cognitive flexibility refers to various processes which enable behaviors to be modified on the basis of a change in the contingencies between stimuli or responses and their associated outcomes. Reversal learning is a form of cognitive flexibility which measures the ability to adjust responding based on a switch in the stimulus–outcome contingencies of, typically two, perceptually distinct stimuli. Reversal tasks have provided valuable insight into the neural basis of cognitive flexibility, implicating brain regions including the lateral orbitofrontal cortex (lOFC) and dorsomedial prefrontal cortex (dmPFC). However, with two-stimulus reversal, it is difficult to determine whether response errors are due excessive perseveration, deficient learning, or other problems with updating. To address this limitation, we developed a mouse three-choice touchscreen-based visual reversal task, in which the contingencies of two stimuli were switched on reversal but a third, simultaneously presented, stimulus was never reinforced. We found that, in male C57BL/6J mice, responding at the previously rewarded stimulus predominated over the newly and never-reinforced stimuli during early reversal. Next, we showed that acute pharmacological inhibition of lOFC, but not dmPFC, impaired early reversal performance, relative to noninactivated controls. Interestingly, however, lOFC inactivation deficits were characterized by increased choice of the never-reinforced stimulus and a decrease in (perseverative-like) responding at the previously rewarded stimulus. These effects are inconsistent with the historical notion of lOFC mediating response inhibition and closer to recent views of the lOFC's role in response/outcome tracking. Overall, these findings provide initial support the utility of this novel paradigm for studying cognitive flexibility and its underlying neural substrates.
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spelling pubmed-62985392020-01-01 A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice Piantadosi, Patrick T. Lieberman, Abby G. Pickens, Charles L. Bergstrom, Hadley C. Holmes, Andrew Learn Mem Brief Communication Cognitive flexibility refers to various processes which enable behaviors to be modified on the basis of a change in the contingencies between stimuli or responses and their associated outcomes. Reversal learning is a form of cognitive flexibility which measures the ability to adjust responding based on a switch in the stimulus–outcome contingencies of, typically two, perceptually distinct stimuli. Reversal tasks have provided valuable insight into the neural basis of cognitive flexibility, implicating brain regions including the lateral orbitofrontal cortex (lOFC) and dorsomedial prefrontal cortex (dmPFC). However, with two-stimulus reversal, it is difficult to determine whether response errors are due excessive perseveration, deficient learning, or other problems with updating. To address this limitation, we developed a mouse three-choice touchscreen-based visual reversal task, in which the contingencies of two stimuli were switched on reversal but a third, simultaneously presented, stimulus was never reinforced. We found that, in male C57BL/6J mice, responding at the previously rewarded stimulus predominated over the newly and never-reinforced stimuli during early reversal. Next, we showed that acute pharmacological inhibition of lOFC, but not dmPFC, impaired early reversal performance, relative to noninactivated controls. Interestingly, however, lOFC inactivation deficits were characterized by increased choice of the never-reinforced stimulus and a decrease in (perseverative-like) responding at the previously rewarded stimulus. These effects are inconsistent with the historical notion of lOFC mediating response inhibition and closer to recent views of the lOFC's role in response/outcome tracking. Overall, these findings provide initial support the utility of this novel paradigm for studying cognitive flexibility and its underlying neural substrates. Cold Spring Harbor Laboratory Press 2019-01 /pmc/articles/PMC6298539/ /pubmed/30559117 http://dx.doi.org/10.1101/lm.048264.118 Text en Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This is a work of the US Government.
spellingShingle Brief Communication
Piantadosi, Patrick T.
Lieberman, Abby G.
Pickens, Charles L.
Bergstrom, Hadley C.
Holmes, Andrew
A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title_full A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title_fullStr A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title_full_unstemmed A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title_short A novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
title_sort novel multichoice touchscreen paradigm for assessing cognitive flexibility in mice
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6298539/
https://www.ncbi.nlm.nih.gov/pubmed/30559117
http://dx.doi.org/10.1101/lm.048264.118
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