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Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity
Multiple system atrophy (MSA) is a neurodegenerative movement disorder characterized by parkinsonian symptoms and cerebellar symptoms. Sleep disturbances also play a crucial role in MSA. One of the most convincing animal models in MSA research is the PLP α-SYN model, but to date no studies on sleep...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222844/ https://www.ncbi.nlm.nih.gov/pubmed/28119583 http://dx.doi.org/10.3389/fnbeh.2016.00252 |
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author | Härtner, Lorenz Keil, Tobias W. M. Kreuzer, Matthias Fritz, Eva Maria Wenning, Gregor K. Stefanova, Nadia Fenzl, Thomas |
author_facet | Härtner, Lorenz Keil, Tobias W. M. Kreuzer, Matthias Fritz, Eva Maria Wenning, Gregor K. Stefanova, Nadia Fenzl, Thomas |
author_sort | Härtner, Lorenz |
collection | PubMed |
description | Multiple system atrophy (MSA) is a neurodegenerative movement disorder characterized by parkinsonian symptoms and cerebellar symptoms. Sleep disturbances also play a crucial role in MSA. One of the most convincing animal models in MSA research is the PLP α-SYN model, but to date no studies on sleep disturbances in this mouse model, frequently found in MSA patients are available. We identified spectral shifts within the EEG of the model, strikingly resembling results of clinical studies. We also characterized muscle activity during REM sleep, which is one of the key symptoms in REM sleep behavioral disorder. Spectral shifts and REM sleep-linked muscle activity were age dependent, supporting Face Validity of the PLP α-SYN model. We also strongly suggest our findings to be critically evaluated for Predictive Validity in future studies. Currently, research on MSA lacks potential compounds attenuating or curing MSA. Future drugs must prove its potential in animal models, for this our study provides potential biomarkers. |
format | Online Article Text |
id | pubmed-5222844 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52228442017-01-24 Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity Härtner, Lorenz Keil, Tobias W. M. Kreuzer, Matthias Fritz, Eva Maria Wenning, Gregor K. Stefanova, Nadia Fenzl, Thomas Front Behav Neurosci Neuroscience Multiple system atrophy (MSA) is a neurodegenerative movement disorder characterized by parkinsonian symptoms and cerebellar symptoms. Sleep disturbances also play a crucial role in MSA. One of the most convincing animal models in MSA research is the PLP α-SYN model, but to date no studies on sleep disturbances in this mouse model, frequently found in MSA patients are available. We identified spectral shifts within the EEG of the model, strikingly resembling results of clinical studies. We also characterized muscle activity during REM sleep, which is one of the key symptoms in REM sleep behavioral disorder. Spectral shifts and REM sleep-linked muscle activity were age dependent, supporting Face Validity of the PLP α-SYN model. We also strongly suggest our findings to be critically evaluated for Predictive Validity in future studies. Currently, research on MSA lacks potential compounds attenuating or curing MSA. Future drugs must prove its potential in animal models, for this our study provides potential biomarkers. Frontiers Media S.A. 2017-01-10 /pmc/articles/PMC5222844/ /pubmed/28119583 http://dx.doi.org/10.3389/fnbeh.2016.00252 Text en Copyright © 2017 Härtner, Keil, Kreuzer, Fritz, Wenning, Stefanova and Fenzl. http://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) or licensor 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 Härtner, Lorenz Keil, Tobias W. M. Kreuzer, Matthias Fritz, Eva Maria Wenning, Gregor K. Stefanova, Nadia Fenzl, Thomas Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title | Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title_full | Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title_fullStr | Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title_full_unstemmed | Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title_short | Distinct Parameters in the EEG of the PLP α-SYN Mouse Model for Multiple System Atrophy Reinforce Face Validity |
title_sort | distinct parameters in the eeg of the plp α-syn mouse model for multiple system atrophy reinforce face validity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222844/ https://www.ncbi.nlm.nih.gov/pubmed/28119583 http://dx.doi.org/10.3389/fnbeh.2016.00252 |
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