Acute Modulation of Left Ventricular Control by Selective Intracardiac Sympathetic Denervation
- PMID: 36752452
- DOI: 10.1016/j.jacep.2022.10.013
Acute Modulation of Left Ventricular Control by Selective Intracardiac Sympathetic Denervation
Abstract
Background: The sympathetic nervous system plays an integral role in cardiac physiology. Nerve fibers innervating the left ventricle are amenable to transvenous catheter stimulation along the coronary sinus (CS).
Objectives: The aim of the present study was to modulate left ventricular control by selective intracardiac sympathetic denervation.
Methods: First, the impact of epicardial CS ablation on cardiac electrophysiology was studied in a Langendorff model of decentralized murine hearts (n = 10 each, ablation and control groups). Second, the impact of transvenous, anatomically driven axotomy by catheter-based radiofrequency ablation via the CS was evaluated in healthy sheep (n = 8) before and during stellate ganglion stimulation.
Results: CS ablation prolonged epicardial ventricular refractory period without (41.8 ± 8.4 ms vs 53.0 ± 13.5 ms; P = 0.049) and with β1-2-adrenergic receptor blockade (47.8 ± 7.8 ms vs 73.1 ± 13.2 ms; P < 0.001) in mice. Supported by neuromorphological studies illustrating a circumferential CS neural network, intracardiac axotomy by catheter ablation via the CS in healthy sheep diminished the blood pressure increase during stellate ganglion stimulation (Δ systolic blood pressure 21.9 ± 10.9 mm Hg vs 10.5 ± 12.0 mm Hg; P = 0.023; Δ diastolic blood pressure 9.0 ± 5.5 mm Hg vs 3.0 ± 3.5 mm Hg; P = 0.039).
Conclusions: Transvenous, anatomically driven axotomy targeting nerve fibers along the CS enables acute modulation of left ventricular control by selective intracardiac sympathetic denervation.
Keywords: catheter ablation; coronary sinus; intracardiac sympathetic denervation; intrinsic cardiac nervous system; left ventricular sympathetic denervation.
Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures This work was supported by the German Centre for Cardiovascular Research, Berlin, Germany (FKZ 81Z0710112 to Dr Meyer). The authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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