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Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration

Although low-energy extracorporeal cardiac shock wave (ECSW) therapy represents an attractive non-invasive treatment option for ischaemic heart disease, the precise mechanisms of its action and influence on the cardiac tissue remain obscure. The goal of this study was to evaluate the effects of SW a...

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Autores principales: Di Meglio, Franca, Nurzynska, Daria, Castaldo, Clotilde, Miraglia, Rita, Romano, Veronica, De Angelis, Antonella, Piegari, Elena, Russo, Sergio, Montagnani, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822862/
https://www.ncbi.nlm.nih.gov/pubmed/21790971
http://dx.doi.org/10.1111/j.1582-4934.2011.01393.x
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author Di Meglio, Franca
Nurzynska, Daria
Castaldo, Clotilde
Miraglia, Rita
Romano, Veronica
De Angelis, Antonella
Piegari, Elena
Russo, Sergio
Montagnani, Stefania
author_facet Di Meglio, Franca
Nurzynska, Daria
Castaldo, Clotilde
Miraglia, Rita
Romano, Veronica
De Angelis, Antonella
Piegari, Elena
Russo, Sergio
Montagnani, Stefania
author_sort Di Meglio, Franca
collection PubMed
description Although low-energy extracorporeal cardiac shock wave (ECSW) therapy represents an attractive non-invasive treatment option for ischaemic heart disease, the precise mechanisms of its action and influence on the cardiac tissue remain obscure. The goal of this study was to evaluate the effects of SW application on cardiac function and structure. Four-month-old Fisher 344 rats were subjected to ECSW therapy. Echocardiographic measurements of cardiac function were performed at baseline and at 1 and 3 months after treatment. Signs of inflammation, apoptosis and fibrosis were evaluated by immunohistochemistry in the control and treated hearts. ECSW application did not provoke arrhythmia or increase the troponin-I level. At all time points, the left ventricular ejection fraction and fractional shortening remained stable. Histological analysis revealed neither differences in the extracellular matrix collagen content nor the presence of fibrosis; similarly, there were no signs of inflammation. Moreover, a population of cardiac cells that responded eagerly to ECSW application in the adult heart was identified; c-kit–positive, Ki67-positive, orthochromatic cells, corresponding to cardiac primitive cells, were 2.65-fold more numerous in the treated myocardium. In conclusion, non-invasive ECSW therapy is a safe and effective way of activating cardiac stem cells and myocardial regeneration. Because many factors influence cellular turnover in the ischaemic myocardium during the course of ischaemic heart disease, cardiac remodelling, and heart failure progression, studies to identify the optimal treatment time are warranted.
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spelling pubmed-38228622015-03-27 Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration Di Meglio, Franca Nurzynska, Daria Castaldo, Clotilde Miraglia, Rita Romano, Veronica De Angelis, Antonella Piegari, Elena Russo, Sergio Montagnani, Stefania J Cell Mol Med Original Articles Although low-energy extracorporeal cardiac shock wave (ECSW) therapy represents an attractive non-invasive treatment option for ischaemic heart disease, the precise mechanisms of its action and influence on the cardiac tissue remain obscure. The goal of this study was to evaluate the effects of SW application on cardiac function and structure. Four-month-old Fisher 344 rats were subjected to ECSW therapy. Echocardiographic measurements of cardiac function were performed at baseline and at 1 and 3 months after treatment. Signs of inflammation, apoptosis and fibrosis were evaluated by immunohistochemistry in the control and treated hearts. ECSW application did not provoke arrhythmia or increase the troponin-I level. At all time points, the left ventricular ejection fraction and fractional shortening remained stable. Histological analysis revealed neither differences in the extracellular matrix collagen content nor the presence of fibrosis; similarly, there were no signs of inflammation. Moreover, a population of cardiac cells that responded eagerly to ECSW application in the adult heart was identified; c-kit–positive, Ki67-positive, orthochromatic cells, corresponding to cardiac primitive cells, were 2.65-fold more numerous in the treated myocardium. In conclusion, non-invasive ECSW therapy is a safe and effective way of activating cardiac stem cells and myocardial regeneration. Because many factors influence cellular turnover in the ischaemic myocardium during the course of ischaemic heart disease, cardiac remodelling, and heart failure progression, studies to identify the optimal treatment time are warranted. Blackwell Publishing Ltd 2012-04 2012-04-16 /pmc/articles/PMC3822862/ /pubmed/21790971 http://dx.doi.org/10.1111/j.1582-4934.2011.01393.x Text en Copyright © 2012 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.
spellingShingle Original Articles
Di Meglio, Franca
Nurzynska, Daria
Castaldo, Clotilde
Miraglia, Rita
Romano, Veronica
De Angelis, Antonella
Piegari, Elena
Russo, Sergio
Montagnani, Stefania
Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title_full Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title_fullStr Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title_full_unstemmed Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title_short Cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
title_sort cardiac shock wave therapy: assessment of safety and new insights into mechanisms of tissue regeneration
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822862/
https://www.ncbi.nlm.nih.gov/pubmed/21790971
http://dx.doi.org/10.1111/j.1582-4934.2011.01393.x
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