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Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization

Malignant ventricular arrhythmias (VA) after acute myocardial infarction remain a major threat. Aim of this study was to characterize the electrophysiological and autonomic sequelae of cardiac ischemia and reperfusion (I/R) in mice during the first week post incident. Left ventricular function was s...

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Autores principales: Clasen, Lukas, Angendohr, Stephan, Becher, Stefanie, Bartsch, Benedikt, Enkel, Stephan, Meyer, Christian, Kelm, Malte, Makimoto, Hisaki, Klöcker, Nikolaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082073/
https://www.ncbi.nlm.nih.gov/pubmed/37029160
http://dx.doi.org/10.1038/s41598-023-32346-5
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author Clasen, Lukas
Angendohr, Stephan
Becher, Stefanie
Bartsch, Benedikt
Enkel, Stephan
Meyer, Christian
Kelm, Malte
Makimoto, Hisaki
Klöcker, Nikolaj
author_facet Clasen, Lukas
Angendohr, Stephan
Becher, Stefanie
Bartsch, Benedikt
Enkel, Stephan
Meyer, Christian
Kelm, Malte
Makimoto, Hisaki
Klöcker, Nikolaj
author_sort Clasen, Lukas
collection PubMed
description Malignant ventricular arrhythmias (VA) after acute myocardial infarction remain a major threat. Aim of this study was to characterize the electrophysiological and autonomic sequelae of cardiac ischemia and reperfusion (I/R) in mice during the first week post incident. Left ventricular function was serially assessed using transthoracic echocardiography. VA were quantified by telemetric electrocardiogram (ECG) recordings and electrophysiological studies on the 2nd and 7th day after I/R. Cardiac autonomic function was evaluated by heart rate variability (HRV) and heart rate turbulence (HRT). Infarct size was quantified by planimetric measures. I/R caused significant myocardial scarring and diminished left ventricular ejection fraction. The ECG intervals QRS, QT, QT(c), and JT(c) were prolonged in I/R mice. Both spontaneous VA scored higher and the inducibility of VA was raised in I/R mice. An analysis of HRV and HRT indicated a relative reduction in parasympathetic activity and disturbed baroreflex sensitivity up to 7 days after I/R. In summary, during the first week after I/R, the murine heart reflects essential features of the human heart after myocardial infarction, including a greater vulnerability for VA and a decreased parasympathetic tone accompanied by decelerated depolarization and repolarization parameters.
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spelling pubmed-100820732023-04-09 Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization Clasen, Lukas Angendohr, Stephan Becher, Stefanie Bartsch, Benedikt Enkel, Stephan Meyer, Christian Kelm, Malte Makimoto, Hisaki Klöcker, Nikolaj Sci Rep Article Malignant ventricular arrhythmias (VA) after acute myocardial infarction remain a major threat. Aim of this study was to characterize the electrophysiological and autonomic sequelae of cardiac ischemia and reperfusion (I/R) in mice during the first week post incident. Left ventricular function was serially assessed using transthoracic echocardiography. VA were quantified by telemetric electrocardiogram (ECG) recordings and electrophysiological studies on the 2nd and 7th day after I/R. Cardiac autonomic function was evaluated by heart rate variability (HRV) and heart rate turbulence (HRT). Infarct size was quantified by planimetric measures. I/R caused significant myocardial scarring and diminished left ventricular ejection fraction. The ECG intervals QRS, QT, QT(c), and JT(c) were prolonged in I/R mice. Both spontaneous VA scored higher and the inducibility of VA was raised in I/R mice. An analysis of HRV and HRT indicated a relative reduction in parasympathetic activity and disturbed baroreflex sensitivity up to 7 days after I/R. In summary, during the first week after I/R, the murine heart reflects essential features of the human heart after myocardial infarction, including a greater vulnerability for VA and a decreased parasympathetic tone accompanied by decelerated depolarization and repolarization parameters. Nature Publishing Group UK 2023-04-07 /pmc/articles/PMC10082073/ /pubmed/37029160 http://dx.doi.org/10.1038/s41598-023-32346-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Clasen, Lukas
Angendohr, Stephan
Becher, Stefanie
Bartsch, Benedikt
Enkel, Stephan
Meyer, Christian
Kelm, Malte
Makimoto, Hisaki
Klöcker, Nikolaj
Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title_full Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title_fullStr Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title_full_unstemmed Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title_short Cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
title_sort cardiac ischemia and reperfusion in mice: a comprehensive hemodynamic, electrocardiographic and electrophysiological characterization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082073/
https://www.ncbi.nlm.nih.gov/pubmed/37029160
http://dx.doi.org/10.1038/s41598-023-32346-5
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