Pharmacological inhibition of acetylcholine-regulated potassium current (

Atrial fibrillation Cholinergic activation IK,ACh Rats Sleep apnea

Journal

Heart rhythm O2
ISSN: 2666-5018
Titre abrégé: Heart Rhythm O2
Pays: United States
ID NLM: 101768511

Informations de publication

Date de publication:
Feb 2022
Historique:
entrez: 4 3 2022
pubmed: 5 3 2022
medline: 5 3 2022
Statut: epublish

Résumé

In obstructive sleep apnea (OSA), intermittent hypoxemia and intrathoracic pressure fluctuations may increase atrial fibrillation (AF) susceptibility by cholinergic activation. To investigate short-term atrial electrophysiological consequences of obstructive respiratory events, simulated by intermittent negative upper airway pressure (INAP), and the role of atrial acetylcholine-regulated potassium current ( In sedated (2% isoflurane), spontaneously breathing rats, INAP was applied noninvasively by a negative pressure device for 1 minute, followed by a resting period of 4 minutes. INAP was applied repeatedly throughout 70 minutes, followed by a 2-hour recovery period. Atrial effective refractory period (AERP) and AF inducibility were determined throughout the protocol. To study INAP-induced In vehicle-treated rats, repetitive INAP shortened AERP (37 ± 3 ms vs baseline 44 ± 3 ms; Short-term simulated OSA is associated with a progressive, but transient, AERP shortening and a PKC

Sections du résumé

BACKGROUND BACKGROUND
In obstructive sleep apnea (OSA), intermittent hypoxemia and intrathoracic pressure fluctuations may increase atrial fibrillation (AF) susceptibility by cholinergic activation.
OBJECTIVE OBJECTIVE
To investigate short-term atrial electrophysiological consequences of obstructive respiratory events, simulated by intermittent negative upper airway pressure (INAP), and the role of atrial acetylcholine-regulated potassium current (
METHODS METHODS
In sedated (2% isoflurane), spontaneously breathing rats, INAP was applied noninvasively by a negative pressure device for 1 minute, followed by a resting period of 4 minutes. INAP was applied repeatedly throughout 70 minutes, followed by a 2-hour recovery period. Atrial effective refractory period (AERP) and AF inducibility were determined throughout the protocol. To study INAP-induced
RESULTS RESULTS
In vehicle-treated rats, repetitive INAP shortened AERP (37 ± 3 ms vs baseline 44 ± 3 ms;
CONCLUSION CONCLUSIONS
Short-term simulated OSA is associated with a progressive, but transient, AERP shortening and a PKC

Identifiants

pubmed: 35243441
doi: 10.1016/j.hroo.2021.11.013
pii: S2666-5018(21)00223-3
pmc: PMC8859790
doi:

Types de publication

Journal Article

Langues

eng

Pagination

97-104

Informations de copyright

© 2021 Heart Rhythm Society. Published by Elsevier Inc.

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Auteurs

Benedikt Linz (B)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Anne Hauge Thostrup (AH)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Arnela Saljic (A)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Institute of Pharmacology, West German Heart and Vascular Centre, University of Duisburg-Essen, Duisburg, Germany.

Karlijn Rombouts (K)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Julie Norup Hertel (JN)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Mathias Hohl (M)

Klinik für Innere Medizin III, Universität des Saarlandes, Homburg/Saar, Germany.

James Milnes (J)

Xention Ltd, Newmarket, United Kingdom.

Jacob Tfelt-Hansen (J)

Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Department of Forensic Medicine, Faculty of Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Dominik Linz (D)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Centre for Heart Rhythm Disorders, South Australian Health and Medical Research Institute, Royal Adelaide Hospital, University of Adelaide, Adelaide, Australia.
Department of Cardiology, Maastricht University Medical Centre, Maastricht, the Netherlands.

Thomas Jespersen (T)

Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Classifications MeSH