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Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice
Tooth loss or incorrect positioning causes occlusal disharmony. Furthermore, tooth loss and atrial fibrillation (AF) are both risk factors for ischemic stroke and coronary heart disease. Therefore, we hypothesized that occlusal disharmony-induced stress increases susceptibility to AF, and we designe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426945/ https://www.ncbi.nlm.nih.gov/pubmed/32792672 http://dx.doi.org/10.1038/s41598-020-70791-8 |
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author | Suita, Kenji Yagisawa, Yuka Ohnuki, Yoshiki Umeki, Daisuke Nariyama, Megumi Ito, Aiko Hayakawa, Yoshio Matsuo, Ichiro Mototani, Yasumasa Saeki, Yasutake Okumura, Satoshi |
author_facet | Suita, Kenji Yagisawa, Yuka Ohnuki, Yoshiki Umeki, Daisuke Nariyama, Megumi Ito, Aiko Hayakawa, Yoshio Matsuo, Ichiro Mototani, Yasumasa Saeki, Yasutake Okumura, Satoshi |
author_sort | Suita, Kenji |
collection | PubMed |
description | Tooth loss or incorrect positioning causes occlusal disharmony. Furthermore, tooth loss and atrial fibrillation (AF) are both risk factors for ischemic stroke and coronary heart disease. Therefore, we hypothesized that occlusal disharmony-induced stress increases susceptibility to AF, and we designed the present study to test this idea in mice. Bite-opening (BO) was done by cementing a suitable appliance onto the mandibular incisor to cause occlusal disharmony by increasing the vertical height of occlusion by 0.7 mm for a period of 2 weeks. AF susceptibility, evaluated in terms of the duration of AF induced by transesophageal burst pacing, was significantly increased concomitantly with atrial remodeling, including fibrosis, myocyte apoptosis and oxidative DNA damage, in BO mice. The BO-induced atrial remodeling was associated with increased calmodulin kinase II-mediated ryanodine receptor 2 phosphorylation on serine 2814, as well as inhibition of Akt phosphorylation. However, co-treatment with propranolol, a non-selective β-blocker, ameliorated these changes in BO mice. These data suggest that improvement of occlusal disharmony by means of orthodontic treatment might be helpful in the treatment or prevention of AF. |
format | Online Article Text |
id | pubmed-7426945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74269452020-08-14 Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice Suita, Kenji Yagisawa, Yuka Ohnuki, Yoshiki Umeki, Daisuke Nariyama, Megumi Ito, Aiko Hayakawa, Yoshio Matsuo, Ichiro Mototani, Yasumasa Saeki, Yasutake Okumura, Satoshi Sci Rep Article Tooth loss or incorrect positioning causes occlusal disharmony. Furthermore, tooth loss and atrial fibrillation (AF) are both risk factors for ischemic stroke and coronary heart disease. Therefore, we hypothesized that occlusal disharmony-induced stress increases susceptibility to AF, and we designed the present study to test this idea in mice. Bite-opening (BO) was done by cementing a suitable appliance onto the mandibular incisor to cause occlusal disharmony by increasing the vertical height of occlusion by 0.7 mm for a period of 2 weeks. AF susceptibility, evaluated in terms of the duration of AF induced by transesophageal burst pacing, was significantly increased concomitantly with atrial remodeling, including fibrosis, myocyte apoptosis and oxidative DNA damage, in BO mice. The BO-induced atrial remodeling was associated with increased calmodulin kinase II-mediated ryanodine receptor 2 phosphorylation on serine 2814, as well as inhibition of Akt phosphorylation. However, co-treatment with propranolol, a non-selective β-blocker, ameliorated these changes in BO mice. These data suggest that improvement of occlusal disharmony by means of orthodontic treatment might be helpful in the treatment or prevention of AF. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426945/ /pubmed/32792672 http://dx.doi.org/10.1038/s41598-020-70791-8 Text en © The Author(s) 2020 Open AccessThis 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/. |
spellingShingle | Article Suita, Kenji Yagisawa, Yuka Ohnuki, Yoshiki Umeki, Daisuke Nariyama, Megumi Ito, Aiko Hayakawa, Yoshio Matsuo, Ichiro Mototani, Yasumasa Saeki, Yasutake Okumura, Satoshi Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title | Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title_full | Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title_fullStr | Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title_full_unstemmed | Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title_short | Effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
title_sort | effects of occlusal disharmony on susceptibility to atrial fibrillation in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426945/ https://www.ncbi.nlm.nih.gov/pubmed/32792672 http://dx.doi.org/10.1038/s41598-020-70791-8 |
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