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Wide-area low-energy surface stimulation of large mammalian ventricular tissue
The epicardial and endocardial surfaces of the heart are attractive targets to administer antiarrhythmic electrotherapies. Electrically stimulating wide areas of the surfaces of small mammalian ventricles is straightforward given the relatively small scale of their myocardial dimensions compared to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825186/ https://www.ncbi.nlm.nih.gov/pubmed/31676789 http://dx.doi.org/10.1038/s41598-019-51364-w |
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author | Moreno, Angel Walton, Richard D. Constantin, Marion Bernus, Olivier Vigmond, Edward J. Bayer, Jason D. |
author_facet | Moreno, Angel Walton, Richard D. Constantin, Marion Bernus, Olivier Vigmond, Edward J. Bayer, Jason D. |
author_sort | Moreno, Angel |
collection | PubMed |
description | The epicardial and endocardial surfaces of the heart are attractive targets to administer antiarrhythmic electrotherapies. Electrically stimulating wide areas of the surfaces of small mammalian ventricles is straightforward given the relatively small scale of their myocardial dimensions compared to the tissue space constant and electrical field. However, it has yet to be proven for larger mammalian hearts with tissue properties and ventricular dimensions closer to humans. Our goal was to address the feasibility and impact of wide-area electrical stimulation on the ventricular surfaces of large mammalian hearts at different stimulus strengths. This was accomplished by placing long line electrodes on the ventricular surfaces of pig hearts that span wide areas, and activating them individually. Stimulus efficacy was assessed and compared between surfaces, and tissue viability was evaluated. Activation time was dependent on stimulation strength and location, achieving uniform linear stimulation at 9x threshold strength. Endocardial stimulation activated more tissue transmurally than epicardial stimulation, which could be considered a potential target for future cardiac electrotherapies. Overall, our results indicate that electrically stimulating wide areas of the ventricular surfaces of large mammals is achievable with line electrodes, minimal tissue damage, and energies under the human pain threshold (100 mJ). |
format | Online Article Text |
id | pubmed-6825186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68251862019-11-12 Wide-area low-energy surface stimulation of large mammalian ventricular tissue Moreno, Angel Walton, Richard D. Constantin, Marion Bernus, Olivier Vigmond, Edward J. Bayer, Jason D. Sci Rep Article The epicardial and endocardial surfaces of the heart are attractive targets to administer antiarrhythmic electrotherapies. Electrically stimulating wide areas of the surfaces of small mammalian ventricles is straightforward given the relatively small scale of their myocardial dimensions compared to the tissue space constant and electrical field. However, it has yet to be proven for larger mammalian hearts with tissue properties and ventricular dimensions closer to humans. Our goal was to address the feasibility and impact of wide-area electrical stimulation on the ventricular surfaces of large mammalian hearts at different stimulus strengths. This was accomplished by placing long line electrodes on the ventricular surfaces of pig hearts that span wide areas, and activating them individually. Stimulus efficacy was assessed and compared between surfaces, and tissue viability was evaluated. Activation time was dependent on stimulation strength and location, achieving uniform linear stimulation at 9x threshold strength. Endocardial stimulation activated more tissue transmurally than epicardial stimulation, which could be considered a potential target for future cardiac electrotherapies. Overall, our results indicate that electrically stimulating wide areas of the ventricular surfaces of large mammals is achievable with line electrodes, minimal tissue damage, and energies under the human pain threshold (100 mJ). Nature Publishing Group UK 2019-11-01 /pmc/articles/PMC6825186/ /pubmed/31676789 http://dx.doi.org/10.1038/s41598-019-51364-w Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Moreno, Angel Walton, Richard D. Constantin, Marion Bernus, Olivier Vigmond, Edward J. Bayer, Jason D. Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title | Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title_full | Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title_fullStr | Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title_full_unstemmed | Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title_short | Wide-area low-energy surface stimulation of large mammalian ventricular tissue |
title_sort | wide-area low-energy surface stimulation of large mammalian ventricular tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825186/ https://www.ncbi.nlm.nih.gov/pubmed/31676789 http://dx.doi.org/10.1038/s41598-019-51364-w |
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