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Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome

Fragile X syndrome (FXS) is characterized by sensory hyper-sensitivity, and animal models suggest that neuronal hyper-excitability contributes to this phenotype. To understand how sensory dysfunction develops in FXS, we used the rat model (FMR-KO) to quantify the maturation of cortical visual respon...

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Autores principales: Berzhanskaya, Julia, Phillips, Marnie A., Shen, Jing, Colonnese, Matthew T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964352/
https://www.ncbi.nlm.nih.gov/pubmed/27465362
http://dx.doi.org/10.1038/srep30769
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author Berzhanskaya, Julia
Phillips, Marnie A.
Shen, Jing
Colonnese, Matthew T.
author_facet Berzhanskaya, Julia
Phillips, Marnie A.
Shen, Jing
Colonnese, Matthew T.
author_sort Berzhanskaya, Julia
collection PubMed
description Fragile X syndrome (FXS) is characterized by sensory hyper-sensitivity, and animal models suggest that neuronal hyper-excitability contributes to this phenotype. To understand how sensory dysfunction develops in FXS, we used the rat model (FMR-KO) to quantify the maturation of cortical visual responses from the onset of responsiveness prior to eye-opening, through age equivalents of human juveniles. Rather than hyper-excitability, visual responses before eye-opening had reduced spike rates and an absence of early gamma oscillations, a marker for normal thalamic function at this age. Despite early hypo-excitability, the developmental trajectory of visual responses in FMR-KO rats was normal, and showed the expected loss of visually evoked bursting at the same age as wild-type, two days before eye-opening. At later ages, during the third and fourth post-natal weeks, signs of mild hyper-excitability emerged. These included an increase in the visually-evoked firing of regular spiking, presumptive excitatory, neurons, and a reduced firing of fast-spiking, presumptive inhibitory, neurons. Our results show that early network changes in the FMR-KO rat arise at ages equivalent to fetal humans and have consequences for excitability that are opposite those found in adults. This suggests identification and treatment should begin early, and be tailored in an age-appropriate manner.
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spelling pubmed-49643522016-08-08 Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome Berzhanskaya, Julia Phillips, Marnie A. Shen, Jing Colonnese, Matthew T. Sci Rep Article Fragile X syndrome (FXS) is characterized by sensory hyper-sensitivity, and animal models suggest that neuronal hyper-excitability contributes to this phenotype. To understand how sensory dysfunction develops in FXS, we used the rat model (FMR-KO) to quantify the maturation of cortical visual responses from the onset of responsiveness prior to eye-opening, through age equivalents of human juveniles. Rather than hyper-excitability, visual responses before eye-opening had reduced spike rates and an absence of early gamma oscillations, a marker for normal thalamic function at this age. Despite early hypo-excitability, the developmental trajectory of visual responses in FMR-KO rats was normal, and showed the expected loss of visually evoked bursting at the same age as wild-type, two days before eye-opening. At later ages, during the third and fourth post-natal weeks, signs of mild hyper-excitability emerged. These included an increase in the visually-evoked firing of regular spiking, presumptive excitatory, neurons, and a reduced firing of fast-spiking, presumptive inhibitory, neurons. Our results show that early network changes in the FMR-KO rat arise at ages equivalent to fetal humans and have consequences for excitability that are opposite those found in adults. This suggests identification and treatment should begin early, and be tailored in an age-appropriate manner. Nature Publishing Group 2016-07-28 /pmc/articles/PMC4964352/ /pubmed/27465362 http://dx.doi.org/10.1038/srep30769 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Berzhanskaya, Julia
Phillips, Marnie A.
Shen, Jing
Colonnese, Matthew T.
Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title_full Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title_fullStr Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title_full_unstemmed Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title_short Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome
title_sort sensory hypo-excitability in a rat model of fetal development in fragile x syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964352/
https://www.ncbi.nlm.nih.gov/pubmed/27465362
http://dx.doi.org/10.1038/srep30769
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