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Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis
BACKGROUND: The prevalence of atrial fibrillation (AF) is significantly higher in rheumatoid arthritis (RA) patients, but the underlying mechanisms remain poorly understood. The goal of this study was to assess the effects of RA on AF susceptibility and atrial arrhythmogenic remodeling in a rat mode...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779041/ https://www.ncbi.nlm.nih.gov/pubmed/29269354 http://dx.doi.org/10.1161/JAHA.117.007320 |
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author | Dai, Hui Wang, Xiaoyu Yin, Shuangli Zhang, Yun Han, Yu Yang, Ning Xu, Jicheng Sun, Li Yuan, Yue Sheng, Li Gong, Yongtai Li, Yue |
author_facet | Dai, Hui Wang, Xiaoyu Yin, Shuangli Zhang, Yun Han, Yu Yang, Ning Xu, Jicheng Sun, Li Yuan, Yue Sheng, Li Gong, Yongtai Li, Yue |
author_sort | Dai, Hui |
collection | PubMed |
description | BACKGROUND: The prevalence of atrial fibrillation (AF) is significantly higher in rheumatoid arthritis (RA) patients, but the underlying mechanisms remain poorly understood. The goal of this study was to assess the effects of RA on AF susceptibility and atrial arrhythmogenic remodeling in a rat model of RA. METHODS AND RESULTS: Collagen‐induced arthritis was induced in rats by immunization with type II collagen in Freund's incomplete adjuvant. Among the rats that developed arthritis, AF susceptibility and atrial remodeling were examined 8 weeks after the primary immunization. AF inducibility and duration were substantially increased in collagen‐induced arthritis rats, and AF duration was significantly and positively correlated with the serum IL‐6 and TNF‐α levels. Rats with collagen‐induced arthritis showed prolonged atrial conduction time with no changes in the atrial effective refractory period. Atrial conduction delay was accompanied by significantly increased atrial fibrosis. In addition, atrial structural and autonomic remodeling, including left atrial dilation, apoptosis and autophagy of atrial myocytes, and atrial heterogeneous sympathetic hyperinnervation, was observed. Interestingly, we found that collagen‐induced arthritis had no significant effects on connexins, Nav1.5, and the main ion channels' protein expressions in atria. CONCLUSIONS: We demonstrated that RA increased AF susceptibility by inducing AF‐promoting atrial remodeling. This study may provide insights into mechanisms underlying RA‐induced AF and validate a model that is suitable for further mechanistic and therapeutic exploration. |
format | Online Article Text |
id | pubmed-5779041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57790412018-01-26 Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis Dai, Hui Wang, Xiaoyu Yin, Shuangli Zhang, Yun Han, Yu Yang, Ning Xu, Jicheng Sun, Li Yuan, Yue Sheng, Li Gong, Yongtai Li, Yue J Am Heart Assoc Original Research BACKGROUND: The prevalence of atrial fibrillation (AF) is significantly higher in rheumatoid arthritis (RA) patients, but the underlying mechanisms remain poorly understood. The goal of this study was to assess the effects of RA on AF susceptibility and atrial arrhythmogenic remodeling in a rat model of RA. METHODS AND RESULTS: Collagen‐induced arthritis was induced in rats by immunization with type II collagen in Freund's incomplete adjuvant. Among the rats that developed arthritis, AF susceptibility and atrial remodeling were examined 8 weeks after the primary immunization. AF inducibility and duration were substantially increased in collagen‐induced arthritis rats, and AF duration was significantly and positively correlated with the serum IL‐6 and TNF‐α levels. Rats with collagen‐induced arthritis showed prolonged atrial conduction time with no changes in the atrial effective refractory period. Atrial conduction delay was accompanied by significantly increased atrial fibrosis. In addition, atrial structural and autonomic remodeling, including left atrial dilation, apoptosis and autophagy of atrial myocytes, and atrial heterogeneous sympathetic hyperinnervation, was observed. Interestingly, we found that collagen‐induced arthritis had no significant effects on connexins, Nav1.5, and the main ion channels' protein expressions in atria. CONCLUSIONS: We demonstrated that RA increased AF susceptibility by inducing AF‐promoting atrial remodeling. This study may provide insights into mechanisms underlying RA‐induced AF and validate a model that is suitable for further mechanistic and therapeutic exploration. John Wiley and Sons Inc. 2017-12-21 /pmc/articles/PMC5779041/ /pubmed/29269354 http://dx.doi.org/10.1161/JAHA.117.007320 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Dai, Hui Wang, Xiaoyu Yin, Shuangli Zhang, Yun Han, Yu Yang, Ning Xu, Jicheng Sun, Li Yuan, Yue Sheng, Li Gong, Yongtai Li, Yue Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title | Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title_full | Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title_fullStr | Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title_full_unstemmed | Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title_short | Atrial Fibrillation Promotion in a Rat Model of Rheumatoid Arthritis |
title_sort | atrial fibrillation promotion in a rat model of rheumatoid arthritis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5779041/ https://www.ncbi.nlm.nih.gov/pubmed/29269354 http://dx.doi.org/10.1161/JAHA.117.007320 |
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