Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts

Autores
Vargas, Lorena Alejandra; Carrizo Velásquez, Fernanda Elisabeth; Álvarez, Bernardo Víctor
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
NBC Na+/HCO3 − cotransporter (NBCn1) and NHE1 Na+/H+ exchanger have been associated with cardiac disorders and recently located in coronary endothelial cells (CEC) and cardiomyocytes mitochondria, respectively. Mitochondrial NHE1 blockade delays permeability transition pore (MPTP) opening and reduces superoxide levels, two critical events exacerbated in cells of diseased hearts. Conversely, activation of NBCn1 prevented apoptosis in CEC subjected to ischemic stress. We characterized the role of the NHE1 and NBCn1 transporters in heart mitochondria from hypertrophic (SHR) and control (Wistar) rats. Expression of NHE1 was analyzed in left ventricular mitochondrial lysates (LVML), by immunoblots. NHE1 expression increased by ~40% in SHR compared to control (P < 0.05, n = 4). To examine NHE1-mediated Na+/H+ exchange activity in cardiac hypertrophy, mitochondria were loaded with BCECF-AM dye and the maximal rate of pHm change measured after the addition of 50 mM NaCl. SHR mitochondria had greater changes in pHm compared to Wistar, 0.10 ± 0.01 vs. 0.06 ± 0.01, respectively (P < 0.05, n = 5). In addition, mitochondrial suspensions from SHR and control myocardium were exposed to 200 μM CaCl2 to induce MPTP opening (light-scattering decrease, LSD) and swelling. Surprisingly, SHR rats showed smaller LSD and a reduction in mitochondrial swelling, 67 ± 10% (n = 15), compared to control, 100 ± 8% (n = 13). NBC inhibition with S0859 (1 μM) significantly increased swelling in both control 139 ± 10% (n = 8) and SHR 115 ± 10% (n = 4). Finally, NBCn1 Na+/HCO3 − cotransporter increased by twofold its expression in SHR LVML, compared to normal (P < 0.05, n = 5). We conclude that increased NBCn1 activity may play a compensatory role in hypertrophic hearts, protecting mitochondria from Ca-induced MPTP opening and swelling.
Este trabajo tiene una expresión editorial de preocupación y asimismo una retractación (ver "Documentos relacionados").
Centro de Investigaciones Cardiovasculares
Materia
Ciencias Médicas
Hypertrophy
Mitochondrial permeability transition pore
Myocardium
NBCn1 Na+/HCO3 - cotransporter
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/102178

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/102178
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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic heartsVargas, Lorena AlejandraCarrizo Velásquez, Fernanda ElisabethÁlvarez, Bernardo VíctorCiencias MédicasHypertrophyMitochondrial permeability transition poreMyocardiumNBCn1 Na+/HCO3 - cotransporterNBC Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter (NBCn1) and NHE1 Na<sup>+</sup>/H<sup>+</sup> exchanger have been associated with cardiac disorders and recently located in coronary endothelial cells (CEC) and cardiomyocytes mitochondria, respectively. Mitochondrial NHE1 blockade delays permeability transition pore (MPTP) opening and reduces superoxide levels, two critical events exacerbated in cells of diseased hearts. Conversely, activation of NBCn1 prevented apoptosis in CEC subjected to ischemic stress. We characterized the role of the NHE1 and NBCn1 transporters in heart mitochondria from hypertrophic (SHR) and control (Wistar) rats. Expression of NHE1 was analyzed in left ventricular mitochondrial lysates (LVML), by immunoblots. NHE1 expression increased by ~40% in SHR compared to control (P < 0.05, n = 4). To examine NHE1-mediated Na<sup>+</sup>/H<sup>+</sup> exchange activity in cardiac hypertrophy, mitochondria were loaded with BCECF-AM dye and the maximal rate of pHm change measured after the addition of 50 mM NaCl. SHR mitochondria had greater changes in pHm compared to Wistar, 0.10 ± 0.01 vs. 0.06 ± 0.01, respectively (P < 0.05, n = 5). In addition, mitochondrial suspensions from SHR and control myocardium were exposed to 200 μM CaCl2 to induce MPTP opening (light-scattering decrease, LSD) and swelling. Surprisingly, SHR rats showed smaller LSD and a reduction in mitochondrial swelling, 67 ± 10% (n = 15), compared to control, 100 ± 8% (n = 13). NBC inhibition with S0859 (1 μM) significantly increased swelling in both control 139 ± 10% (n = 8) and SHR 115 ± 10% (n = 4). Finally, NBCn1 Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter increased by twofold its expression in SHR LVML, compared to normal (P < 0.05, n = 5). We conclude that increased NBCn1 activity may play a compensatory role in hypertrophic hearts, protecting mitochondria from Ca<sup2+</sup>-induced MPTP opening and swelling.Este trabajo tiene una expresión editorial de preocupación y asimismo una retractación (ver "Documentos relacionados").Centro de Investigaciones Cardiovasculares2017-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/102178enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/54406info:eu-repo/semantics/altIdentifier/issn/0300-8428info:eu-repo/semantics/altIdentifier/doi/10.1007/s00395-017-0604-7info:eu-repo/semantics/altIdentifier/hdl/11336/54406info:eu-repo/semantics/reference/hdl/10915/131587info:eu-repo/semantics/reference/hdl/10915/144992info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:20:10Zoai:sedici.unlp.edu.ar:10915/102178Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:20:11.145SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
title Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
spellingShingle Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
Vargas, Lorena Alejandra
Ciencias Médicas
Hypertrophy
Mitochondrial permeability transition pore
Myocardium
NBCn1 Na+/HCO3 - cotransporter
title_short Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
title_full Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
title_fullStr Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
title_full_unstemmed Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
title_sort Compensatory role of the NBCn1 sodium/bicarbonate cotransporter on Ca<SUP>2+</SUP>-induced mitochondrial swelling in hypertrophic hearts
dc.creator.none.fl_str_mv Vargas, Lorena Alejandra
Carrizo Velásquez, Fernanda Elisabeth
Álvarez, Bernardo Víctor
author Vargas, Lorena Alejandra
author_facet Vargas, Lorena Alejandra
Carrizo Velásquez, Fernanda Elisabeth
Álvarez, Bernardo Víctor
author_role author
author2 Carrizo Velásquez, Fernanda Elisabeth
Álvarez, Bernardo Víctor
author2_role author
author
dc.subject.none.fl_str_mv Ciencias Médicas
Hypertrophy
Mitochondrial permeability transition pore
Myocardium
NBCn1 Na+/HCO3 - cotransporter
topic Ciencias Médicas
Hypertrophy
Mitochondrial permeability transition pore
Myocardium
NBCn1 Na+/HCO3 - cotransporter
dc.description.none.fl_txt_mv NBC Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter (NBCn1) and NHE1 Na<sup>+</sup>/H<sup>+</sup> exchanger have been associated with cardiac disorders and recently located in coronary endothelial cells (CEC) and cardiomyocytes mitochondria, respectively. Mitochondrial NHE1 blockade delays permeability transition pore (MPTP) opening and reduces superoxide levels, two critical events exacerbated in cells of diseased hearts. Conversely, activation of NBCn1 prevented apoptosis in CEC subjected to ischemic stress. We characterized the role of the NHE1 and NBCn1 transporters in heart mitochondria from hypertrophic (SHR) and control (Wistar) rats. Expression of NHE1 was analyzed in left ventricular mitochondrial lysates (LVML), by immunoblots. NHE1 expression increased by ~40% in SHR compared to control (P < 0.05, n = 4). To examine NHE1-mediated Na<sup>+</sup>/H<sup>+</sup> exchange activity in cardiac hypertrophy, mitochondria were loaded with BCECF-AM dye and the maximal rate of pHm change measured after the addition of 50 mM NaCl. SHR mitochondria had greater changes in pHm compared to Wistar, 0.10 ± 0.01 vs. 0.06 ± 0.01, respectively (P < 0.05, n = 5). In addition, mitochondrial suspensions from SHR and control myocardium were exposed to 200 μM CaCl2 to induce MPTP opening (light-scattering decrease, LSD) and swelling. Surprisingly, SHR rats showed smaller LSD and a reduction in mitochondrial swelling, 67 ± 10% (n = 15), compared to control, 100 ± 8% (n = 13). NBC inhibition with S0859 (1 μM) significantly increased swelling in both control 139 ± 10% (n = 8) and SHR 115 ± 10% (n = 4). Finally, NBCn1 Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter increased by twofold its expression in SHR LVML, compared to normal (P < 0.05, n = 5). We conclude that increased NBCn1 activity may play a compensatory role in hypertrophic hearts, protecting mitochondria from Ca<sup2+</sup>-induced MPTP opening and swelling.
Este trabajo tiene una expresión editorial de preocupación y asimismo una retractación (ver "Documentos relacionados").
Centro de Investigaciones Cardiovasculares
description NBC Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter (NBCn1) and NHE1 Na<sup>+</sup>/H<sup>+</sup> exchanger have been associated with cardiac disorders and recently located in coronary endothelial cells (CEC) and cardiomyocytes mitochondria, respectively. Mitochondrial NHE1 blockade delays permeability transition pore (MPTP) opening and reduces superoxide levels, two critical events exacerbated in cells of diseased hearts. Conversely, activation of NBCn1 prevented apoptosis in CEC subjected to ischemic stress. We characterized the role of the NHE1 and NBCn1 transporters in heart mitochondria from hypertrophic (SHR) and control (Wistar) rats. Expression of NHE1 was analyzed in left ventricular mitochondrial lysates (LVML), by immunoblots. NHE1 expression increased by ~40% in SHR compared to control (P < 0.05, n = 4). To examine NHE1-mediated Na<sup>+</sup>/H<sup>+</sup> exchange activity in cardiac hypertrophy, mitochondria were loaded with BCECF-AM dye and the maximal rate of pHm change measured after the addition of 50 mM NaCl. SHR mitochondria had greater changes in pHm compared to Wistar, 0.10 ± 0.01 vs. 0.06 ± 0.01, respectively (P < 0.05, n = 5). In addition, mitochondrial suspensions from SHR and control myocardium were exposed to 200 μM CaCl2 to induce MPTP opening (light-scattering decrease, LSD) and swelling. Surprisingly, SHR rats showed smaller LSD and a reduction in mitochondrial swelling, 67 ± 10% (n = 15), compared to control, 100 ± 8% (n = 13). NBC inhibition with S0859 (1 μM) significantly increased swelling in both control 139 ± 10% (n = 8) and SHR 115 ± 10% (n = 4). Finally, NBCn1 Na<sup>+</sup>/HCO<sub>3</sub> − cotransporter increased by twofold its expression in SHR LVML, compared to normal (P < 0.05, n = 5). We conclude that increased NBCn1 activity may play a compensatory role in hypertrophic hearts, protecting mitochondria from Ca<sup2+</sup>-induced MPTP opening and swelling.
publishDate 2017
dc.date.none.fl_str_mv 2017-03
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info:eu-repo/semantics/reference/hdl/10915/131587
info:eu-repo/semantics/reference/hdl/10915/144992
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