Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling

Abstract Autonomic dysregulation plays a key role in the development and progression of heart failure (HF). Vagal nerve stimulation (VNS) may be a promising therapeutic approach. However, the outcomes from clinical trials evaluating VNS in HF have been mixed, and the mechanisms underlying this treat...

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Main Authors: Emma J. Radcliffe, Charles M. Pearman, Amy Watkins, Michael Lawless, Graeme J. Kirkwood, Sophie N. Saxton, David A. Eisner, Andrew W. Trafford
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14321
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spelling doaj-94a805943b3141dc99028ded915d88c62020-11-25T03:25:17ZengWileyPhysiological Reports2051-817X2020-01-0182n/an/a10.14814/phy2.14321Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction couplingEmma J. Radcliffe0Charles M. Pearman1Amy Watkins2Michael Lawless3Graeme J. Kirkwood4Sophie N. Saxton5David A. Eisner6Andrew W. Trafford7Unit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKUnit of Cardiac Physiology Institute of Cardiovascular Sciences Manchester Academic Health Sciences Centre The University of Manchester Manchester UKAbstract Autonomic dysregulation plays a key role in the development and progression of heart failure (HF). Vagal nerve stimulation (VNS) may be a promising therapeutic approach. However, the outcomes from clinical trials evaluating VNS in HF have been mixed, and the mechanisms underlying this treatment remain poorly understood. Intermittent high‐frequency VNS (pulse width 300 µs, 30 Hz stimulation, 30 s on, and 300 s off) was used in healthy sheep and sheep in which established HF had been induced by 4 weeks rapid ventricular pacing to assess (a) the effects of VNS on intrinsic cardiac vagal tone, (b) whether VNS delays the progression of established HF, and (c) whether high‐frequency VNS affects the regulation of cardiomyocyte calcium handling in health and disease. VNS had no effect on resting heart rate or intrinsic vagal tone in the healthy heart. Although fewer VNS‐treated animals showed subjective signs of heart failure at 6 weeks, overall VNS did not slow the progression of clinical or echocardiographic signs of HF. Chronic VNS did not affect left ventricular cardiomyocyte calcium handling in healthy sheep. Rapid ventricular pacing decreased the L‐type calcium current and calcium transient amplitude, but chronic VNS did not rescue dysfunctional calcium handling. Overall, high‐frequency VNS did not prevent progression of established HF or influence cellular excitation–contraction coupling. However, a different model of HF or selection of different stimulation parameters may have yielded different results. These results highlight the need for greater insight into VNS dosing and parameter selection and a deeper understanding of its physiological effects.https://doi.org/10.14814/phy2.14321calciumheart failureparasympathetictachycardia‐induced cardiomyopathyvagal nerve stimulation
collection DOAJ
language English
format Article
sources DOAJ
author Emma J. Radcliffe
Charles M. Pearman
Amy Watkins
Michael Lawless
Graeme J. Kirkwood
Sophie N. Saxton
David A. Eisner
Andrew W. Trafford
spellingShingle Emma J. Radcliffe
Charles M. Pearman
Amy Watkins
Michael Lawless
Graeme J. Kirkwood
Sophie N. Saxton
David A. Eisner
Andrew W. Trafford
Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
Physiological Reports
calcium
heart failure
parasympathetic
tachycardia‐induced cardiomyopathy
vagal nerve stimulation
author_facet Emma J. Radcliffe
Charles M. Pearman
Amy Watkins
Michael Lawless
Graeme J. Kirkwood
Sophie N. Saxton
David A. Eisner
Andrew W. Trafford
author_sort Emma J. Radcliffe
title Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
title_short Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
title_full Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
title_fullStr Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
title_full_unstemmed Chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
title_sort chronic vagal nerve stimulation has no effect on tachycardia‐induced heart failure progression or excitation–contraction coupling
publisher Wiley
series Physiological Reports
issn 2051-817X
publishDate 2020-01-01
description Abstract Autonomic dysregulation plays a key role in the development and progression of heart failure (HF). Vagal nerve stimulation (VNS) may be a promising therapeutic approach. However, the outcomes from clinical trials evaluating VNS in HF have been mixed, and the mechanisms underlying this treatment remain poorly understood. Intermittent high‐frequency VNS (pulse width 300 µs, 30 Hz stimulation, 30 s on, and 300 s off) was used in healthy sheep and sheep in which established HF had been induced by 4 weeks rapid ventricular pacing to assess (a) the effects of VNS on intrinsic cardiac vagal tone, (b) whether VNS delays the progression of established HF, and (c) whether high‐frequency VNS affects the regulation of cardiomyocyte calcium handling in health and disease. VNS had no effect on resting heart rate or intrinsic vagal tone in the healthy heart. Although fewer VNS‐treated animals showed subjective signs of heart failure at 6 weeks, overall VNS did not slow the progression of clinical or echocardiographic signs of HF. Chronic VNS did not affect left ventricular cardiomyocyte calcium handling in healthy sheep. Rapid ventricular pacing decreased the L‐type calcium current and calcium transient amplitude, but chronic VNS did not rescue dysfunctional calcium handling. Overall, high‐frequency VNS did not prevent progression of established HF or influence cellular excitation–contraction coupling. However, a different model of HF or selection of different stimulation parameters may have yielded different results. These results highlight the need for greater insight into VNS dosing and parameter selection and a deeper understanding of its physiological effects.
topic calcium
heart failure
parasympathetic
tachycardia‐induced cardiomyopathy
vagal nerve stimulation
url https://doi.org/10.14814/phy2.14321
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