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Redox-Active Drug, MnTE-2-PyP5+, 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.
Afiliación
  • Barbosa AM; Department of Biotechnology, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Sarmento-Neto JF; Heart Circle, Recife, Brazil.
  • Menezes Filho JER; Department of Chemistry, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Jesus ICG; Department of Physiology, Federal University of Sergipe, Aracaju, Brazil.
  • Souza DS; Department of Physiology and Biophysics, Federal University of Minas Gerais, Belo Horizonte, Brazil.
  • Vasconcelos VMN; Department of Physiology, Federal University of Sergipe, Aracaju, Brazil.
  • Gomes FDL; Department of Biotechnology, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Lara A; Department of Biotechnology, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Araújo JSS; Department of Biotechnology, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Mattos SS; Heart Circle, Recife, Brazil.
  • Vasconcelos CML; Department of Public Health, Federal University of Paraiba, Joao Pessoa, Brazil.
  • Guatimosim S; Heart Circle, Recife, Brazil.
  • Cruz JS; Department of Physiology, Federal University of Sergipe, Aracaju, Brazil.
  • Batinic-Haberle I; Department of Physiology and Biophysics, Federal University of Minas Gerais, Belo Horizonte, Brazil.
  • Araújo DAM; Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, Brazil.
  • Rebouças JS; Department of Radiation Oncology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Gomes ER; Department of Biotechnology, Federal University of Paraiba, Joao Pessoa, Brazil.
Oxid Med Cell Longev ; 2020: 4850697, 2020.
Article en En | MEDLINE | ID: mdl-32273944
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-PyP5+), 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 Ca2+ dynamics, L-type Ca2+ currents, Ca2+ spark frequency, intracellular reactive oxygen species (ROS) levels, and cardiomyocyte and cardiac contractility, in control and MnTE-2-PyP5+-treated cells, hearts, or animals. Cells and hearts were treated with 20 µM MnTE-2-PyP5+ 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-PyP5+ reduced intracellular Ca2+ transient amplitude, without altering cell contractility. Whereas MnTE-2-PyP5+ did not alter basal ROS levels, it was efficient in modulating cardiomyocyte redox state under stress conditions; MnTE-2-PyP5+ reduced Ca2+ spark frequency and increased sarcoplasmic reticulum (SR) Ca2+ load. Accordingly, analysis of isolated perfused rat hearts showed that MnTE-2-PyP5+ preserves cardiac function, increases SR Ca2+ load, and reduces arrhythmia index, indicating an antiarrhythmic effect. In vivo experiments showed that MnTE-2-PyP5+ treatment increased Ca2+ transient, preserved cardiac ejection fraction, and reduced arrhythmia index and duration. MnTE-2-PyP5+ was effective both to prevent and to treat cardiac arrhythmias. CONCLUSION: MnTE-2-PyP5+ prevents and treats cardiac arrhythmias in rats. In contrast to most antiarrhythmic drugs, MnTE-2-PyP5+ preserves cardiac contractile function, arising, thus, as a prospective therapeutic for improvement of cardiac arrhythmia treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidación-Reducción / Arritmias Cardíacas / Sistema Cardiovascular / Metaloporfirinas Límite: Animals Idioma: En Revista: Oxid Med Cell Longev Asunto de la revista: METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidación-Reducción / Arritmias Cardíacas / Sistema Cardiovascular / Metaloporfirinas Límite: Animals Idioma: En Revista: Oxid Med Cell Longev Asunto de la revista: METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Estados Unidos