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Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with Experimental Chagas Disease
BACKGROUND: Chagas disease is a tropical parasitic disease caused by the flagellate protozoan Trypanosoma cruzi. Chagasic cardiomyopathy is characterized by disorders of autonomic regulation and action potential conduction in the acute and chronic phases of infection. Although tumor necrosis factor...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032299/ https://www.ncbi.nlm.nih.gov/pubmed/23877744 http://dx.doi.org/10.5935/abc.20130149 |
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author | Rodríguez-Angulo, Héctor García, Oscar Castillo, Endher Cardenas, Edward Marques, Juan Mijares, Alfredo |
author_facet | Rodríguez-Angulo, Héctor García, Oscar Castillo, Endher Cardenas, Edward Marques, Juan Mijares, Alfredo |
author_sort | Rodríguez-Angulo, Héctor |
collection | PubMed |
description | BACKGROUND: Chagas disease is a tropical parasitic disease caused by the flagellate protozoan Trypanosoma cruzi. Chagasic cardiomyopathy is characterized by disorders of autonomic regulation and action potential conduction in the acute and chronic phases of infection. Although tumor necrosis factor alpha (TNF-α) has been linked to cardiomyopathy in experimental models and in patients with Chagas disease, other reports suggest that TNF-α may exert anti-parasitic actions during the acute phase of infection. OBJECTIVES: This study aimed to determine the effects of a soluble TNF-α blocker, etanercept, on electrocardiographic parameters in the acute phase of experimental infection with Trypanosoma cruzi. METHODS: Electrocardiograms were obtained from untreated infected mice and infected mice who were treated with etanercept 7 days after infection. ECG wave and heart rate variability parameters were determined using Chart for Windows. RESULTS: Etanercept treatment resulted in a low QRS voltage and decreased heart rate variability compared with no treatment. However, the treated mice exhibited a delay in the fall of the survival curve during the acute phase. CONCLUSION: The results of this study suggest that although etanercept treatment promotes survival in mice infected with a virulent T. cruzi strain, TNF-α blockade generates a low voltage complex and autonomic dysfunction during the acute phase of infection. These findings indicate that mortality during the acute phase can be attributed to a systemic inflammatory response rather than cardiac dysfunction. |
format | Online Article Text |
id | pubmed-4032299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Cardiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-40322992014-05-27 Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with Experimental Chagas Disease Rodríguez-Angulo, Héctor García, Oscar Castillo, Endher Cardenas, Edward Marques, Juan Mijares, Alfredo Arq Bras Cardiol Original Article BACKGROUND: Chagas disease is a tropical parasitic disease caused by the flagellate protozoan Trypanosoma cruzi. Chagasic cardiomyopathy is characterized by disorders of autonomic regulation and action potential conduction in the acute and chronic phases of infection. Although tumor necrosis factor alpha (TNF-α) has been linked to cardiomyopathy in experimental models and in patients with Chagas disease, other reports suggest that TNF-α may exert anti-parasitic actions during the acute phase of infection. OBJECTIVES: This study aimed to determine the effects of a soluble TNF-α blocker, etanercept, on electrocardiographic parameters in the acute phase of experimental infection with Trypanosoma cruzi. METHODS: Electrocardiograms were obtained from untreated infected mice and infected mice who were treated with etanercept 7 days after infection. ECG wave and heart rate variability parameters were determined using Chart for Windows. RESULTS: Etanercept treatment resulted in a low QRS voltage and decreased heart rate variability compared with no treatment. However, the treated mice exhibited a delay in the fall of the survival curve during the acute phase. CONCLUSION: The results of this study suggest that although etanercept treatment promotes survival in mice infected with a virulent T. cruzi strain, TNF-α blockade generates a low voltage complex and autonomic dysfunction during the acute phase of infection. These findings indicate that mortality during the acute phase can be attributed to a systemic inflammatory response rather than cardiac dysfunction. Sociedade Brasileira de Cardiologia 2013-09 /pmc/articles/PMC4032299/ /pubmed/23877744 http://dx.doi.org/10.5935/abc.20130149 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Rodríguez-Angulo, Héctor García, Oscar Castillo, Endher Cardenas, Edward Marques, Juan Mijares, Alfredo Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with Experimental Chagas Disease |
title | Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with
Experimental Chagas Disease |
title_full | Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with
Experimental Chagas Disease |
title_fullStr | Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with
Experimental Chagas Disease |
title_full_unstemmed | Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with
Experimental Chagas Disease |
title_short | Etanercept Induces Low QRS Voltage and Autonomic Dysfunction in Mice with
Experimental Chagas Disease |
title_sort | etanercept induces low qrs voltage and autonomic dysfunction in mice with
experimental chagas disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032299/ https://www.ncbi.nlm.nih.gov/pubmed/23877744 http://dx.doi.org/10.5935/abc.20130149 |
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