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Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function

BACKGROUND: Cardiomyopathies remain among the leading causes of death worldwide, despite all efforts and important advances in the development of cardiovascular therapeutics, demonstrating the need for new solutions. Herein, we describe the effects of the redox-active therapeutic Mn(III) meso-tetrak...

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Autores principales: Barbosa, Andrezza M., Sarmento-Neto, José F., Menezes Filho, José E. R., Jesus, Itamar C. G., Souza, Diego S., Vasconcelos, Valério M. N., Gomes, Fagner D. L., Lara, Aline, Araújo, Juliana S. S., Mattos, Sandra S., Vasconcelos, Carla M. L., Guatimosim, Silvia, Cruz, Jader S., Batinic-Haberle, Ines, Araújo, Demetrius A. M., Rebouças, Júlio S., Gomes, Enéas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115175/
https://www.ncbi.nlm.nih.gov/pubmed/32273944
http://dx.doi.org/10.1155/2020/4850697
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author Barbosa, Andrezza M.
Sarmento-Neto, José F.
Menezes Filho, José E. R.
Jesus, Itamar C. G.
Souza, Diego S.
Vasconcelos, Valério M. N.
Gomes, Fagner D. L.
Lara, Aline
Araújo, Juliana S. S.
Mattos, Sandra S.
Vasconcelos, Carla M. L.
Guatimosim, Silvia
Cruz, Jader S.
Batinic-Haberle, Ines
Araújo, Demetrius A. M.
Rebouças, Júlio S.
Gomes, Enéas R.
author_facet Barbosa, Andrezza M.
Sarmento-Neto, José F.
Menezes Filho, José E. R.
Jesus, Itamar C. G.
Souza, Diego S.
Vasconcelos, Valério M. N.
Gomes, Fagner D. L.
Lara, Aline
Araújo, Juliana S. S.
Mattos, Sandra S.
Vasconcelos, Carla M. L.
Guatimosim, Silvia
Cruz, Jader S.
Batinic-Haberle, Ines
Araújo, Demetrius A. M.
Rebouças, Júlio S.
Gomes, Enéas R.
author_sort Barbosa, Andrezza M.
collection PubMed
description BACKGROUND: Cardiomyopathies remain among the leading causes of death worldwide, despite all efforts and important advances in the development of cardiovascular therapeutics, demonstrating the need for new solutions. Herein, we describe the effects of the redox-active therapeutic Mn(III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin, AEOL10113, BMX-010 (MnTE-2-PyP(5+)), on rat heart as an entry to new strategies to circumvent cardiomyopathies. METHODS: Wistar rats weighing 250-300 g were used in both in vitro and in vivo experiments, to analyze intracellular Ca(2+) dynamics, L-type Ca(2+) currents, Ca(2+) spark frequency, intracellular reactive oxygen species (ROS) levels, and cardiomyocyte and cardiac contractility, in control and MnTE-2-PyP(5+)-treated cells, hearts, or animals. Cells and hearts were treated with 20 μM MnTE-2-PyP(5+) and animals with 1 mg/kg, i.p. daily. Additionally, we performed electrocardiographic and echocardiographic analysis. RESULTS: Using isolated rat cardiomyocytes, we observed that MnTE-2-PyP(5+) reduced intracellular Ca(2+) transient amplitude, without altering cell contractility. Whereas MnTE-2-PyP(5+) did not alter basal ROS levels, it was efficient in modulating cardiomyocyte redox state under stress conditions; MnTE-2-PyP(5+) reduced Ca(2+) spark frequency and increased sarcoplasmic reticulum (SR) Ca(2+) load. Accordingly, analysis of isolated perfused rat hearts showed that MnTE-2-PyP(5+) preserves cardiac function, increases SR Ca(2+) load, and reduces arrhythmia index, indicating an antiarrhythmic effect. In vivo experiments showed that MnTE-2-PyP(5+) treatment increased Ca(2+) transient, preserved cardiac ejection fraction, and reduced arrhythmia index and duration. MnTE-2-PyP(5+) was effective both to prevent and to treat cardiac arrhythmias. CONCLUSION: MnTE-2-PyP(5+) prevents and treats cardiac arrhythmias in rats. In contrast to most antiarrhythmic drugs, MnTE-2-PyP(5+) preserves cardiac contractile function, arising, thus, as a prospective therapeutic for improvement of cardiac arrhythmia treatment.
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spelling pubmed-71151752020-04-09 Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function Barbosa, Andrezza M. Sarmento-Neto, José F. Menezes Filho, José E. R. Jesus, Itamar C. G. Souza, Diego S. Vasconcelos, Valério M. N. Gomes, Fagner D. L. Lara, Aline Araújo, Juliana S. S. Mattos, Sandra S. Vasconcelos, Carla M. L. Guatimosim, Silvia Cruz, Jader S. Batinic-Haberle, Ines Araújo, Demetrius A. M. Rebouças, Júlio S. Gomes, Enéas R. Oxid Med Cell Longev Research Article BACKGROUND: Cardiomyopathies remain among the leading causes of death worldwide, despite all efforts and important advances in the development of cardiovascular therapeutics, demonstrating the need for new solutions. Herein, we describe the effects of the redox-active therapeutic Mn(III) meso-tetrakis(N-ethylpyridinium-2-yl)porphyrin, AEOL10113, BMX-010 (MnTE-2-PyP(5+)), on rat heart as an entry to new strategies to circumvent cardiomyopathies. METHODS: Wistar rats weighing 250-300 g were used in both in vitro and in vivo experiments, to analyze intracellular Ca(2+) dynamics, L-type Ca(2+) currents, Ca(2+) spark frequency, intracellular reactive oxygen species (ROS) levels, and cardiomyocyte and cardiac contractility, in control and MnTE-2-PyP(5+)-treated cells, hearts, or animals. Cells and hearts were treated with 20 μM MnTE-2-PyP(5+) and animals with 1 mg/kg, i.p. daily. Additionally, we performed electrocardiographic and echocardiographic analysis. RESULTS: Using isolated rat cardiomyocytes, we observed that MnTE-2-PyP(5+) reduced intracellular Ca(2+) transient amplitude, without altering cell contractility. Whereas MnTE-2-PyP(5+) did not alter basal ROS levels, it was efficient in modulating cardiomyocyte redox state under stress conditions; MnTE-2-PyP(5+) reduced Ca(2+) spark frequency and increased sarcoplasmic reticulum (SR) Ca(2+) load. Accordingly, analysis of isolated perfused rat hearts showed that MnTE-2-PyP(5+) preserves cardiac function, increases SR Ca(2+) load, and reduces arrhythmia index, indicating an antiarrhythmic effect. In vivo experiments showed that MnTE-2-PyP(5+) treatment increased Ca(2+) transient, preserved cardiac ejection fraction, and reduced arrhythmia index and duration. MnTE-2-PyP(5+) was effective both to prevent and to treat cardiac arrhythmias. CONCLUSION: MnTE-2-PyP(5+) prevents and treats cardiac arrhythmias in rats. In contrast to most antiarrhythmic drugs, MnTE-2-PyP(5+) preserves cardiac contractile function, arising, thus, as a prospective therapeutic for improvement of cardiac arrhythmia treatment. Hindawi 2020-03-21 /pmc/articles/PMC7115175/ /pubmed/32273944 http://dx.doi.org/10.1155/2020/4850697 Text en Copyright © 2020 Andrezza M. Barbosa et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Barbosa, Andrezza M.
Sarmento-Neto, José F.
Menezes Filho, José E. R.
Jesus, Itamar C. G.
Souza, Diego S.
Vasconcelos, Valério M. N.
Gomes, Fagner D. L.
Lara, Aline
Araújo, Juliana S. S.
Mattos, Sandra S.
Vasconcelos, Carla M. L.
Guatimosim, Silvia
Cruz, Jader S.
Batinic-Haberle, Ines
Araújo, Demetrius A. M.
Rebouças, Júlio S.
Gomes, Enéas R.
Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title_full Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title_fullStr Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title_full_unstemmed Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title_short Redox-Active Drug, MnTE-2-PyP(5+), Prevents and Treats Cardiac Arrhythmias Preserving Heart Contractile Function
title_sort redox-active drug, mnte-2-pyp(5+), prevents and treats cardiac arrhythmias preserving heart contractile function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115175/
https://www.ncbi.nlm.nih.gov/pubmed/32273944
http://dx.doi.org/10.1155/2020/4850697
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