Neuro-Cardio mechanisms in Huntington’s disease and other neurodegenerative disorders
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Published version
Author(s)
Critchley, Bethan
Isalan, Mark
Mielcarek, M
Type
Journal Article
Abstract
Although Huntington’s disease is generally considered to be a
neurological disorder, there is mounting evidence that heart malfunction
plays an important role in disease progression. This is perhaps
not unexpected since both cardiovascular and nervous systems are
strongly connected—both development ally and subsequently in
health and disease. This connection occurs through a system
of central and peripheral neurons that control cardiovascular
performance, while in return the cardiovascular system works
as a sensor for the nervous system to react to physiological
events. Hence, given their permanent interconnectivity, any
pathological events occurring in one system might affect the second. In addition, some pathological signals fromHuntington’s disease might occur simultaneously in both the cardiovascular and nervous systems, since mutant Huntingtin protein is expressed
in both. Here we aim to review the source of HD-related card
iomyopathy in the light of recently-published studies, and to identify
similarities between HD-related cardiomyopathy andother
neuro-cardio disorders.
neurological disorder, there is mounting evidence that heart malfunction
plays an important role in disease progression. This is perhaps
not unexpected since both cardiovascular and nervous systems are
strongly connected—both development ally and subsequently in
health and disease. This connection occurs through a system
of central and peripheral neurons that control cardiovascular
performance, while in return the cardiovascular system works
as a sensor for the nervous system to react to physiological
events. Hence, given their permanent interconnectivity, any
pathological events occurring in one system might affect the second. In addition, some pathological signals fromHuntington’s disease might occur simultaneously in both the cardiovascular and nervous systems, since mutant Huntingtin protein is expressed
in both. Here we aim to review the source of HD-related card
iomyopathy in the light of recently-published studies, and to identify
similarities between HD-related cardiomyopathy andother
neuro-cardio disorders.
Date Issued
2018-05-23
Date Acceptance
2018-04-30
Citation
Frontiers in Physiology, 2018, 9
ISSN
1664-042X
Publisher
Frontiers Media
Journal / Book Title
Frontiers in Physiology
Volume
9
Copyright Statement
© 2018 Critchley, Isalan and Mielcarek. 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 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.
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 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.
Sponsor
Wellcome Trust
Wellcome Trust
Medical Research Council (MRC)
Grant Number
102944/Z/13/Z
102944/Z/13/Z
MC_PC15028
Subjects
Science & Technology
Life Sciences & Biomedicine
Physiology
neuro-cardio disorders
Huntington's disease
cardiomyopathy
CNS
heart failure
DESMIN-RELATED CARDIOMYOPATHY
TRANSGENIC MOUSE MODEL
HEART-FAILURE
PARKINSONS-DISEASE
ALZHEIMERS-DISEASE
PRESENILIN GENES
DYSFUNCTION
METABOLISM
ARRHYTHMIAS
INHIBITION
Huntington’s disease
Publication Status
Published
Article Number
ARTN 559