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Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice
Whereas Huntington’s disease (HD) is unequivocally a neurological disorder, a critical mass of emerging studies highlights the occurrence of peripheral pathology like cardiovascular defects in both animal models and humans. The overt impairment in cardiac function is normally expected to be associat...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314343/ https://www.ncbi.nlm.nih.gov/pubmed/28211486 http://dx.doi.org/10.1038/srep42797 |
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author | Di Pardo, A. Carrizzo, A. Damato, A. Castaldo, S. Amico, E. Capocci, L. Ambrosio, M. Pompeo, F. De Sanctis, C. Spinelli, C. C. Puca, A. A. Remondelli, P. Maglione, V. Vecchione, C. |
author_facet | Di Pardo, A. Carrizzo, A. Damato, A. Castaldo, S. Amico, E. Capocci, L. Ambrosio, M. Pompeo, F. De Sanctis, C. Spinelli, C. C. Puca, A. A. Remondelli, P. Maglione, V. Vecchione, C. |
author_sort | Di Pardo, A. |
collection | PubMed |
description | Whereas Huntington’s disease (HD) is unequivocally a neurological disorder, a critical mass of emerging studies highlights the occurrence of peripheral pathology like cardiovascular defects in both animal models and humans. The overt impairment in cardiac function is normally expected to be associated with peripheral vascular dysfunction, however whether this assumption is reasonable or not in HD is still unknown. In this study we functionally characterized the vascular system in R6/2 mouse model (line 160 CAG), which recapitulates several features of human pathology including cardiac disease. Vascular reactivity in different arterial districts was determined by wire myography in symptomatic R6/2 mice and age-matched wild type (WT) littermates. Disease stage was assessed by using well-validated behavioural tests like rotarod and horizontal ladder task. Surprisingly, no signs of vascular dysfunction were detectable in symptomatic mice and no link with motor phenotype was found. |
format | Online Article Text |
id | pubmed-5314343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53143432017-02-23 Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice Di Pardo, A. Carrizzo, A. Damato, A. Castaldo, S. Amico, E. Capocci, L. Ambrosio, M. Pompeo, F. De Sanctis, C. Spinelli, C. C. Puca, A. A. Remondelli, P. Maglione, V. Vecchione, C. Sci Rep Article Whereas Huntington’s disease (HD) is unequivocally a neurological disorder, a critical mass of emerging studies highlights the occurrence of peripheral pathology like cardiovascular defects in both animal models and humans. The overt impairment in cardiac function is normally expected to be associated with peripheral vascular dysfunction, however whether this assumption is reasonable or not in HD is still unknown. In this study we functionally characterized the vascular system in R6/2 mouse model (line 160 CAG), which recapitulates several features of human pathology including cardiac disease. Vascular reactivity in different arterial districts was determined by wire myography in symptomatic R6/2 mice and age-matched wild type (WT) littermates. Disease stage was assessed by using well-validated behavioural tests like rotarod and horizontal ladder task. Surprisingly, no signs of vascular dysfunction were detectable in symptomatic mice and no link with motor phenotype was found. Nature Publishing Group 2017-02-17 /pmc/articles/PMC5314343/ /pubmed/28211486 http://dx.doi.org/10.1038/srep42797 Text en Copyright © 2017, 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 Di Pardo, A. Carrizzo, A. Damato, A. Castaldo, S. Amico, E. Capocci, L. Ambrosio, M. Pompeo, F. De Sanctis, C. Spinelli, C. C. Puca, A. A. Remondelli, P. Maglione, V. Vecchione, C. Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title | Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title_full | Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title_fullStr | Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title_full_unstemmed | Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title_short | Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington’s disease transgenic R6/2 (160 CAG) mice |
title_sort | motor phenotype is not associated with vascular dysfunction in symptomatic huntington’s disease transgenic r6/2 (160 cag) mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314343/ https://www.ncbi.nlm.nih.gov/pubmed/28211486 http://dx.doi.org/10.1038/srep42797 |
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