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Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model
BACKGROUND: Cardiac contractility modulation (CCM) is non-excitatory electrical stimulation for improving cardiac function. This study aimed to evaluate the effects of CCM on structural and electrical remodeling in a rabbit model of chronic heart failure (CHF). METHODS: Thirty rabbits were randomly...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556184/ https://www.ncbi.nlm.nih.gov/pubmed/33044118 http://dx.doi.org/10.1177/0300060520962910 |
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author | Ning, Bin Zhang, Feifei Song, Xuelian Hao, Qingqing Li, Yingxiao Li, Rong Dang, Yi |
author_facet | Ning, Bin Zhang, Feifei Song, Xuelian Hao, Qingqing Li, Yingxiao Li, Rong Dang, Yi |
author_sort | Ning, Bin |
collection | PubMed |
description | BACKGROUND: Cardiac contractility modulation (CCM) is non-excitatory electrical stimulation for improving cardiac function. This study aimed to evaluate the effects of CCM on structural and electrical remodeling in a rabbit model of chronic heart failure (CHF). METHODS: Thirty rabbits were randomly divided into the sham, CHF, and CCM groups. The CHF model was induced 12 weeks after trans-aortic constriction by pressure unloading and CCM was delivered to the myocardium for 4 weeks. Corrected QT intervals, the ventricular effective refractory period, and inducibility of ventricular tachycardia were measured by an electrophysiological examination. Connective tissue growth factor, galectin-3, Kv4.3, KCNQ1, KCNH2, and connexin 43 protein levels were measured by western blotting. RESULTS: The CHF group had a significantly prolonged corrected QT interval and ventricular effective refractory period, and increased inducibility of ventricular tachycardia. Prominent myocardial fibrosis and increased hydroxyproline content were observed in the CHF group, but these were suppressed in the CCM group. Kv4.3, KCNQ1, KCNH2, and connexin 43 protein levels were significantly lower in the CHF group, but treatment with CCM partially restored their levels. CONCLUSIONS: CCM attenuates myocardial structural and electrical remodeling during CHF. These findings provide evidence for clinical use of CCM in treating CHF. |
format | Online Article Text |
id | pubmed-7556184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75561842020-10-26 Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model Ning, Bin Zhang, Feifei Song, Xuelian Hao, Qingqing Li, Yingxiao Li, Rong Dang, Yi J Int Med Res Pre-Clinical Research Report BACKGROUND: Cardiac contractility modulation (CCM) is non-excitatory electrical stimulation for improving cardiac function. This study aimed to evaluate the effects of CCM on structural and electrical remodeling in a rabbit model of chronic heart failure (CHF). METHODS: Thirty rabbits were randomly divided into the sham, CHF, and CCM groups. The CHF model was induced 12 weeks after trans-aortic constriction by pressure unloading and CCM was delivered to the myocardium for 4 weeks. Corrected QT intervals, the ventricular effective refractory period, and inducibility of ventricular tachycardia were measured by an electrophysiological examination. Connective tissue growth factor, galectin-3, Kv4.3, KCNQ1, KCNH2, and connexin 43 protein levels were measured by western blotting. RESULTS: The CHF group had a significantly prolonged corrected QT interval and ventricular effective refractory period, and increased inducibility of ventricular tachycardia. Prominent myocardial fibrosis and increased hydroxyproline content were observed in the CHF group, but these were suppressed in the CCM group. Kv4.3, KCNQ1, KCNH2, and connexin 43 protein levels were significantly lower in the CHF group, but treatment with CCM partially restored their levels. CONCLUSIONS: CCM attenuates myocardial structural and electrical remodeling during CHF. These findings provide evidence for clinical use of CCM in treating CHF. SAGE Publications 2020-10-12 /pmc/articles/PMC7556184/ /pubmed/33044118 http://dx.doi.org/10.1177/0300060520962910 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Pre-Clinical Research Report Ning, Bin Zhang, Feifei Song, Xuelian Hao, Qingqing Li, Yingxiao Li, Rong Dang, Yi Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title | Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title_full | Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title_fullStr | Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title_full_unstemmed | Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title_short | Cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
title_sort | cardiac contractility modulation attenuates structural and electrical remodeling in a chronic heart failure rabbit model |
topic | Pre-Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556184/ https://www.ncbi.nlm.nih.gov/pubmed/33044118 http://dx.doi.org/10.1177/0300060520962910 |
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