Cargando…

Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts

BACKGROUND: Time-domain and non-linear methods can be used to quantify beat-to-beat repolarization variability but whether measures of repolarization variability can predict ventricular arrhythmogenesis in mice have never been explored. METHODS: Left ventricular monophasic action potentials (MAPs) w...

Descripción completa

Detalles Bibliográficos
Autores principales: Tse, Gary, Hao, Guoliang, Lee, Sharen, Zhou, Jiandong, Zhang, Qingpeng, Du, Yimei, Liu, Tong, Cheng, Shuk Han, Wong, Wing Tak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562203/
https://www.ncbi.nlm.nih.gov/pubmed/34746832
http://dx.doi.org/10.1016/j.crphys.2021.04.001
_version_ 1784593213368041472
author Tse, Gary
Hao, Guoliang
Lee, Sharen
Zhou, Jiandong
Zhang, Qingpeng
Du, Yimei
Liu, Tong
Cheng, Shuk Han
Wong, Wing Tak
author_facet Tse, Gary
Hao, Guoliang
Lee, Sharen
Zhou, Jiandong
Zhang, Qingpeng
Du, Yimei
Liu, Tong
Cheng, Shuk Han
Wong, Wing Tak
author_sort Tse, Gary
collection PubMed
description BACKGROUND: Time-domain and non-linear methods can be used to quantify beat-to-beat repolarization variability but whether measures of repolarization variability can predict ventricular arrhythmogenesis in mice have never been explored. METHODS: Left ventricular monophasic action potentials (MAPs) were recorded during constant right ventricular 8 ​Hz pacing in Langendorff-perfused mouse hearts, in the presence or absence of the gap junction and sodium channel inhibitor heptanol (0.1, 0.5, 1 or 2 ​mM). RESULTS: Under control conditions, mean action potential duration (APD) was 39.4 ​± ​8.1 ​ms. Standard deviation (SD) of APDs was 0.3 ​± ​0.2 ​ms, coefficient of variation was 0.9 ​± ​0.8% and the root mean square (RMS) of successive differences in APDs was 0.15 ​± ​0.14 ​ms. Poincaré plots of APD(n+1) against APD(n) revealed ellipsoid morphologies with a SD along the line-of-identity (SD2) to SD perpendicular to the line-of-identity (SD1) ratio of 4.6 ​± ​2.1. Approximate and sample entropy were 0.61 ​± ​0.12 and 0.76 ​± ​0.26, respectively. Detrended fluctuation analysis revealed short- and long-term fluctuation slopes of 1.49 ​± ​0.27 and 0.81 ​± ​0.36, respectively. Heptanol at 2 ​mM induced ventricular tachycardia in five out of six hearts. None of the above parameters were altered by heptanol during which reproducible electrical activity was observed (KW-ANOVA, P ​> ​0.05). Contrastingly, SD2/SD1 decreased to 2.03 ​± ​0.41, approximate and sample entropy increased to 0.82 ​± ​0.12 and 1.45 ​± ​0.34, and short-term fluctuation slope decreased to 0.82 ​± ​0.19 during the 20-s period preceding spontaneous ventricular tachy-arrhythmias (n ​= ​6, KW-ANOVA, P ​< ​0.05). CONCLUSION: Measures of repolarization variability, such as SD2/SD1, entropy, and fluctuation slope are altered preceding the occurrence of ventricular arrhythmogenesis in mouse hearts. Changes in these variables may allow detection of impending arrhythmias for early intervention.
format Online
Article
Text
id pubmed-8562203
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-85622032021-11-04 Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts Tse, Gary Hao, Guoliang Lee, Sharen Zhou, Jiandong Zhang, Qingpeng Du, Yimei Liu, Tong Cheng, Shuk Han Wong, Wing Tak Curr Res Physiol Research Paper BACKGROUND: Time-domain and non-linear methods can be used to quantify beat-to-beat repolarization variability but whether measures of repolarization variability can predict ventricular arrhythmogenesis in mice have never been explored. METHODS: Left ventricular monophasic action potentials (MAPs) were recorded during constant right ventricular 8 ​Hz pacing in Langendorff-perfused mouse hearts, in the presence or absence of the gap junction and sodium channel inhibitor heptanol (0.1, 0.5, 1 or 2 ​mM). RESULTS: Under control conditions, mean action potential duration (APD) was 39.4 ​± ​8.1 ​ms. Standard deviation (SD) of APDs was 0.3 ​± ​0.2 ​ms, coefficient of variation was 0.9 ​± ​0.8% and the root mean square (RMS) of successive differences in APDs was 0.15 ​± ​0.14 ​ms. Poincaré plots of APD(n+1) against APD(n) revealed ellipsoid morphologies with a SD along the line-of-identity (SD2) to SD perpendicular to the line-of-identity (SD1) ratio of 4.6 ​± ​2.1. Approximate and sample entropy were 0.61 ​± ​0.12 and 0.76 ​± ​0.26, respectively. Detrended fluctuation analysis revealed short- and long-term fluctuation slopes of 1.49 ​± ​0.27 and 0.81 ​± ​0.36, respectively. Heptanol at 2 ​mM induced ventricular tachycardia in five out of six hearts. None of the above parameters were altered by heptanol during which reproducible electrical activity was observed (KW-ANOVA, P ​> ​0.05). Contrastingly, SD2/SD1 decreased to 2.03 ​± ​0.41, approximate and sample entropy increased to 0.82 ​± ​0.12 and 1.45 ​± ​0.34, and short-term fluctuation slope decreased to 0.82 ​± ​0.19 during the 20-s period preceding spontaneous ventricular tachy-arrhythmias (n ​= ​6, KW-ANOVA, P ​< ​0.05). CONCLUSION: Measures of repolarization variability, such as SD2/SD1, entropy, and fluctuation slope are altered preceding the occurrence of ventricular arrhythmogenesis in mouse hearts. Changes in these variables may allow detection of impending arrhythmias for early intervention. Elsevier 2021-04-19 /pmc/articles/PMC8562203/ /pubmed/34746832 http://dx.doi.org/10.1016/j.crphys.2021.04.001 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Tse, Gary
Hao, Guoliang
Lee, Sharen
Zhou, Jiandong
Zhang, Qingpeng
Du, Yimei
Liu, Tong
Cheng, Shuk Han
Wong, Wing Tak
Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title_full Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title_fullStr Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title_full_unstemmed Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title_short Measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated Langendorff-perfused mouse hearts
title_sort measures of repolarization variability predict ventricular arrhythmogenesis in heptanol-treated langendorff-perfused mouse hearts
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8562203/
https://www.ncbi.nlm.nih.gov/pubmed/34746832
http://dx.doi.org/10.1016/j.crphys.2021.04.001
work_keys_str_mv AT tsegary measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT haoguoliang measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT leesharen measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT zhoujiandong measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT zhangqingpeng measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT duyimei measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT liutong measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT chengshukhan measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts
AT wongwingtak measuresofrepolarizationvariabilitypredictventriculararrhythmogenesisinheptanoltreatedlangendorffperfusedmousehearts