Reversible and Irreversible Effects of Electroporation on Contractility and Calcium Homeostasis in Isolated Cardiac Ventricular Myocytes.


Journal

Circulation. Arrhythmia and electrophysiology
ISSN: 1941-3084
Titre abrégé: Circ Arrhythm Electrophysiol
Pays: United States
ID NLM: 101474365

Informations de publication

Date de publication:
11 2022
Historique:
pubmed: 29 10 2022
medline: 19 11 2022
entrez: 28 10 2022
Statut: ppublish

Résumé

Irreversible electroporation is an energy form utilizing high-voltage pulsed electric field, leading to cellular homeostasis disruption and cell death. Recently, irreversible electroporation has shown promising results for the treatment of cardiac arrhythmias. However, reversible and irreversible effects of pulsed electric field on cardiac myocytes remain poorly understood. Here, we evaluated the influence of a monophasic single electric pulse (EP) on the contractility, Ca Isolated rat left ventricular myocytes were electroporated using single monophasic EP of different durations and voltages. Sarcomere length and intracellular Ca Electroporation led to an immediate increase in intracellular Ca Sublethal EP affected rat left ventricular myocytes contractility and disrupted Ca

Sections du résumé

BACKGROUND
Irreversible electroporation is an energy form utilizing high-voltage pulsed electric field, leading to cellular homeostasis disruption and cell death. Recently, irreversible electroporation has shown promising results for the treatment of cardiac arrhythmias. However, reversible and irreversible effects of pulsed electric field on cardiac myocytes remain poorly understood. Here, we evaluated the influence of a monophasic single electric pulse (EP) on the contractility, Ca
METHODS
Isolated rat left ventricular myocytes were electroporated using single monophasic EP of different durations and voltages. Sarcomere length and intracellular Ca
RESULTS
Electroporation led to an immediate increase in intracellular Ca
CONCLUSIONS
Sublethal EP affected rat left ventricular myocytes contractility and disrupted Ca

Identifiants

pubmed: 36306333
doi: 10.1161/CIRCEP.122.011131
pmc: PMC9665944
doi:

Substances chimiques

Calcium SY7Q814VUP

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e011131

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Auteurs

Sébastien Chaigne (S)

IHU LIRYC Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux, France (S.C., M.H., O.B., D.B.).
University of Bordeaux, Inserm, CRCTB U1045, Bordeaux, France (S.C., M.H., O.B., D.B.).
CHU de Bordeaux, Hôpital Cardiologique Haut-Lévêque, Pessac, France (S.C., M.H.).

Daniel C Sigg (DC)

Medtronic Cardiac Ablation Solutions, Minneapolis, MN (D.C.S., M.T.S.).

Mark T Stewart (MT)

Medtronic Cardiac Ablation Solutions, Minneapolis, MN (D.C.S., M.T.S.).

Mélèze Hocini (M)

IHU LIRYC Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux, France (S.C., M.H., O.B., D.B.).
University of Bordeaux, Inserm, CRCTB U1045, Bordeaux, France (S.C., M.H., O.B., D.B.).
CHU de Bordeaux, Hôpital Cardiologique Haut-Lévêque, Pessac, France (S.C., M.H.).

Tina Batista Napotnik (T)

Faculty of Electrical Engineering, University of Ljubljana, Ljubljana, Slovenia (T.B.N., D.M.).

Damijan Miklavčič (D)

Faculty of Electrical Engineering, University of Ljubljana, Ljubljana, Slovenia (T.B.N., D.M.).

Olivier Bernus (O)

IHU LIRYC Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux, France (S.C., M.H., O.B., D.B.).
University of Bordeaux, Inserm, CRCTB U1045, Bordeaux, France (S.C., M.H., O.B., D.B.).

David Benoist (D)

IHU LIRYC Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Bordeaux, France (S.C., M.H., O.B., D.B.).
University of Bordeaux, Inserm, CRCTB U1045, Bordeaux, France (S.C., M.H., O.B., D.B.).

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