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Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity

In this study we sought to determine the effect of daily sucrose consumption in young rats on their subsequent performance in tasks that involve the prefrontal cortex and hippocampus. High levels of sugar consumption have been associated with the development of obesity, however less is known about h...

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Autores principales: Reichelt, Amy C, Killcross, Simon, Hambly, Luke D., Morris, Margaret J., Westbrook, R. Fred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371171/
https://www.ncbi.nlm.nih.gov/pubmed/25776039
http://dx.doi.org/10.1101/lm.038000.114
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author Reichelt, Amy C
Killcross, Simon
Hambly, Luke D.
Morris, Margaret J.
Westbrook, R. Fred
author_facet Reichelt, Amy C
Killcross, Simon
Hambly, Luke D.
Morris, Margaret J.
Westbrook, R. Fred
author_sort Reichelt, Amy C
collection PubMed
description In this study we sought to determine the effect of daily sucrose consumption in young rats on their subsequent performance in tasks that involve the prefrontal cortex and hippocampus. High levels of sugar consumption have been associated with the development of obesity, however less is known about how sugar consumption influences behavioral control and high-order cognitive processes. Of particular concern is the fact that sugar intake is greatest in adolescence, an important neurodevelopmental period. We provided sucrose to rats when they were progressing through puberty and adolescence. Cognitive performance was assessed in adulthood on a task related to executive function, a rodent analog of the Stroop task. We found that sucrose-exposed rats failed to show context-appropriate responding during incongruent stimulus compounds presented at test, indicative of impairments in prefrontal cortex function. Sucrose exposed rats also showed deficits in an on object-in-place recognition memory task, indicating that both prefrontal and hippocampal function was impaired. Analysis of brains showed a reduction in expression of parvalbumin-immunoreactive GABAergic interneurons in the hippocampus and prefrontal cortex, indicating that sucrose consumption during adolescence induced long-term pathology, potentially underpinning the cognitive deficits observed. These results suggest that consumption of high levels of sugar-sweetened beverages by adolescents may also impair neurocognitive functions affecting decision-making and memory, potentially rendering them at risk for developing mental health disorders.
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spelling pubmed-43711712016-04-01 Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity Reichelt, Amy C Killcross, Simon Hambly, Luke D. Morris, Margaret J. Westbrook, R. Fred Learn Mem Research In this study we sought to determine the effect of daily sucrose consumption in young rats on their subsequent performance in tasks that involve the prefrontal cortex and hippocampus. High levels of sugar consumption have been associated with the development of obesity, however less is known about how sugar consumption influences behavioral control and high-order cognitive processes. Of particular concern is the fact that sugar intake is greatest in adolescence, an important neurodevelopmental period. We provided sucrose to rats when they were progressing through puberty and adolescence. Cognitive performance was assessed in adulthood on a task related to executive function, a rodent analog of the Stroop task. We found that sucrose-exposed rats failed to show context-appropriate responding during incongruent stimulus compounds presented at test, indicative of impairments in prefrontal cortex function. Sucrose exposed rats also showed deficits in an on object-in-place recognition memory task, indicating that both prefrontal and hippocampal function was impaired. Analysis of brains showed a reduction in expression of parvalbumin-immunoreactive GABAergic interneurons in the hippocampus and prefrontal cortex, indicating that sucrose consumption during adolescence induced long-term pathology, potentially underpinning the cognitive deficits observed. These results suggest that consumption of high levels of sugar-sweetened beverages by adolescents may also impair neurocognitive functions affecting decision-making and memory, potentially rendering them at risk for developing mental health disorders. Cold Spring Harbor Laboratory Press 2015-04 /pmc/articles/PMC4371171/ /pubmed/25776039 http://dx.doi.org/10.1101/lm.038000.114 Text en © 2015 Reichelt et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Reichelt, Amy C
Killcross, Simon
Hambly, Luke D.
Morris, Margaret J.
Westbrook, R. Fred
Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title_full Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title_fullStr Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title_full_unstemmed Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title_short Impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
title_sort impact of adolescent sucrose access on cognitive control, recognition memory, and parvalbumin immunoreactivity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371171/
https://www.ncbi.nlm.nih.gov/pubmed/25776039
http://dx.doi.org/10.1101/lm.038000.114
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