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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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.
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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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