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Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task

Adolescence is a critical period for the development of higher-order cognitive functions. Unlike in humans, very limited tools are available to assess such cognitive abilities in adolescent rodents. We implemented a modified 5-Choice Serial Reaction Time Task (5CSRTT) to selectively measure attentiv...

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Autores principales: Ciampoli, Mariasole, Contarini, Gabriella, Mereu, Maddalena, Papaleo, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577211/
https://www.ncbi.nlm.nih.gov/pubmed/28855580
http://dx.doi.org/10.1038/s41598-017-10112-8
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author Ciampoli, Mariasole
Contarini, Gabriella
Mereu, Maddalena
Papaleo, Francesco
author_facet Ciampoli, Mariasole
Contarini, Gabriella
Mereu, Maddalena
Papaleo, Francesco
author_sort Ciampoli, Mariasole
collection PubMed
description Adolescence is a critical period for the development of higher-order cognitive functions. Unlike in humans, very limited tools are available to assess such cognitive abilities in adolescent rodents. We implemented a modified 5-Choice Serial Reaction Time Task (5CSRTT) to selectively measure attentiveness, impulsivity, broad monitoring, processing speed and distractibility in adolescent mice. 21-day old C57BL/6J mice reliably acquired this task with no sex-dependent differences in 10–12 days. A protocol previously used in adults was less effective to assess impulsiveness in adolescents, but revealed increased vulnerability in females. Next, we distinctively assessed selective, divided and broad monitoring attention modeling the human Spatial Attentional Resource Allocation Task (SARAT). Finally, we measured susceptibility to distractions using non-predictive cues that selectively disrupted attention. These paradigms were also applied to two genetically modified lines: the dopamine transporter (DAT) and catechol-O-methyltransferase (COMT) heterozygous. Adolescent DAT hypo-functioning mice showed attentional deficits and higher impulsivity as found in adults. In contrast to adults, adolescent COMT hypo-functioning mice showed decreased impulsivity and attentional resilience to distractors. These paradigms open new avenues to study the establishment of higher-order cognitive functions in mice, as well as an effective tool for drug-testing and genetic screenings focused on adolescence.
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spelling pubmed-55772112017-09-01 Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task Ciampoli, Mariasole Contarini, Gabriella Mereu, Maddalena Papaleo, Francesco Sci Rep Article Adolescence is a critical period for the development of higher-order cognitive functions. Unlike in humans, very limited tools are available to assess such cognitive abilities in adolescent rodents. We implemented a modified 5-Choice Serial Reaction Time Task (5CSRTT) to selectively measure attentiveness, impulsivity, broad monitoring, processing speed and distractibility in adolescent mice. 21-day old C57BL/6J mice reliably acquired this task with no sex-dependent differences in 10–12 days. A protocol previously used in adults was less effective to assess impulsiveness in adolescents, but revealed increased vulnerability in females. Next, we distinctively assessed selective, divided and broad monitoring attention modeling the human Spatial Attentional Resource Allocation Task (SARAT). Finally, we measured susceptibility to distractions using non-predictive cues that selectively disrupted attention. These paradigms were also applied to two genetically modified lines: the dopamine transporter (DAT) and catechol-O-methyltransferase (COMT) heterozygous. Adolescent DAT hypo-functioning mice showed attentional deficits and higher impulsivity as found in adults. In contrast to adults, adolescent COMT hypo-functioning mice showed decreased impulsivity and attentional resilience to distractors. These paradigms open new avenues to study the establishment of higher-order cognitive functions in mice, as well as an effective tool for drug-testing and genetic screenings focused on adolescence. Nature Publishing Group UK 2017-08-30 /pmc/articles/PMC5577211/ /pubmed/28855580 http://dx.doi.org/10.1038/s41598-017-10112-8 Text en © The Author(s) 2017 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
Ciampoli, Mariasole
Contarini, Gabriella
Mereu, Maddalena
Papaleo, Francesco
Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title_full Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title_fullStr Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title_full_unstemmed Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title_short Attentional Control in Adolescent Mice Assessed with a Modified Five Choice Serial Reaction Time Task
title_sort attentional control in adolescent mice assessed with a modified five choice serial reaction time task
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577211/
https://www.ncbi.nlm.nih.gov/pubmed/28855580
http://dx.doi.org/10.1038/s41598-017-10112-8
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