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Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome

INTRODUCTION: Fragile X Syndrome (FXS) is a monogenic condition that leads to intellectual disability along with behavioral and learning difficulties. Among behavioral and learning difficulties, cognitive flexibility impairments are among the most commonly reported in FXS, which significantly impact...

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Autores principales: Schmitt, Lauren M., Arzuaga, Anna L., Dapore, Ashley, Duncan, Jason, Patel, Maya, Larson, John R., Erickson, Craig A., Sweeney, John A., Ragozzino, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849779/
https://www.ncbi.nlm.nih.gov/pubmed/36688132
http://dx.doi.org/10.3389/fnbeh.2022.1074682
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author Schmitt, Lauren M.
Arzuaga, Anna L.
Dapore, Ashley
Duncan, Jason
Patel, Maya
Larson, John R.
Erickson, Craig A.
Sweeney, John A.
Ragozzino, Michael E.
author_facet Schmitt, Lauren M.
Arzuaga, Anna L.
Dapore, Ashley
Duncan, Jason
Patel, Maya
Larson, John R.
Erickson, Craig A.
Sweeney, John A.
Ragozzino, Michael E.
author_sort Schmitt, Lauren M.
collection PubMed
description INTRODUCTION: Fragile X Syndrome (FXS) is a monogenic condition that leads to intellectual disability along with behavioral and learning difficulties. Among behavioral and learning difficulties, cognitive flexibility impairments are among the most commonly reported in FXS, which significantly impacts daily living. Despite the extensive use of the Fmr1 knockout (KO) mouse to understand molecular, synaptic and behavioral alterations related to FXS, there has been limited development of translational paradigms to understand cognitive flexibility that can be employed in both animal models and individuals with FXS to facilitate treatment development. METHODS: To begin addressing this limitation, a parallel set of studies were carried out that investigated probabilistic reversal learning along with other behavioral and cognitive tests in individuals with FXS and Fmr1 KO mice. Fifty-five adolescents and adults with FXS (67% male) and 34 age- and sex-matched typically developing controls (62% male) completed an initial probabilistic learning training task and a probabilistic reversal learning task. RESULTS: In males with FXS, both initial probabilistic learning and reversal learning deficits were found. However, in females with FXS, we only observed reversal learning deficits. Reversal learning deficits related to more severe psychiatric features in females with FXS, whereas increased sensitivity to negative feedback (lose:shift errors) unexpectedly appear to be adaptive in males with FXS. Male Fmr1 KO mice exhibited both an initial probabilistic learning and reversal learning deficit compared to that of wildtype (WT) mice. Female Fmr1 KO mice were selectively impaired on probabilistic reversal learning. In a prepotent response inhibition test, both male and female Fmr1 KO mice were impaired in learning to choose a non-preferred spatial location to receive a food reward compared to that of WT mice. Neither male nor female Fmr1 KO mice exhibited a change in anxiety compared to that of WT mice. DISCUSSION: Together, our findings demonstrate strikingly similar sex-dependent learning disturbances across individuals with FXS and Fmr1 KO mice. This suggests the promise of using analogous paradigms of cognitive flexibility across species that may speed treatment development to improve lives of individuals with FXS.
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spelling pubmed-98497792023-01-20 Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome Schmitt, Lauren M. Arzuaga, Anna L. Dapore, Ashley Duncan, Jason Patel, Maya Larson, John R. Erickson, Craig A. Sweeney, John A. Ragozzino, Michael E. Front Behav Neurosci Neuroscience INTRODUCTION: Fragile X Syndrome (FXS) is a monogenic condition that leads to intellectual disability along with behavioral and learning difficulties. Among behavioral and learning difficulties, cognitive flexibility impairments are among the most commonly reported in FXS, which significantly impacts daily living. Despite the extensive use of the Fmr1 knockout (KO) mouse to understand molecular, synaptic and behavioral alterations related to FXS, there has been limited development of translational paradigms to understand cognitive flexibility that can be employed in both animal models and individuals with FXS to facilitate treatment development. METHODS: To begin addressing this limitation, a parallel set of studies were carried out that investigated probabilistic reversal learning along with other behavioral and cognitive tests in individuals with FXS and Fmr1 KO mice. Fifty-five adolescents and adults with FXS (67% male) and 34 age- and sex-matched typically developing controls (62% male) completed an initial probabilistic learning training task and a probabilistic reversal learning task. RESULTS: In males with FXS, both initial probabilistic learning and reversal learning deficits were found. However, in females with FXS, we only observed reversal learning deficits. Reversal learning deficits related to more severe psychiatric features in females with FXS, whereas increased sensitivity to negative feedback (lose:shift errors) unexpectedly appear to be adaptive in males with FXS. Male Fmr1 KO mice exhibited both an initial probabilistic learning and reversal learning deficit compared to that of wildtype (WT) mice. Female Fmr1 KO mice were selectively impaired on probabilistic reversal learning. In a prepotent response inhibition test, both male and female Fmr1 KO mice were impaired in learning to choose a non-preferred spatial location to receive a food reward compared to that of WT mice. Neither male nor female Fmr1 KO mice exhibited a change in anxiety compared to that of WT mice. DISCUSSION: Together, our findings demonstrate strikingly similar sex-dependent learning disturbances across individuals with FXS and Fmr1 KO mice. This suggests the promise of using analogous paradigms of cognitive flexibility across species that may speed treatment development to improve lives of individuals with FXS. Frontiers Media S.A. 2023-01-05 /pmc/articles/PMC9849779/ /pubmed/36688132 http://dx.doi.org/10.3389/fnbeh.2022.1074682 Text en Copyright © 2023 Schmitt, Arzuaga, Dapore, Duncan, Patel, Larson, Erickson, Sweeney and Ragozzino. https://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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
Schmitt, Lauren M.
Arzuaga, Anna L.
Dapore, Ashley
Duncan, Jason
Patel, Maya
Larson, John R.
Erickson, Craig A.
Sweeney, John A.
Ragozzino, Michael E.
Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title_full Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title_fullStr Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title_full_unstemmed Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title_short Parallel learning and cognitive flexibility impairments between Fmr1 knockout mice and individuals with fragile X syndrome
title_sort parallel learning and cognitive flexibility impairments between fmr1 knockout mice and individuals with fragile x syndrome
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849779/
https://www.ncbi.nlm.nih.gov/pubmed/36688132
http://dx.doi.org/10.3389/fnbeh.2022.1074682
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