Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways

Autores
Aiello, Ernesto Alejandro; Villa Abrille, María Celeste; Dulce, Raúl Ariel; Cingolani, Horacio Eugenio; Pérez, Néstor Gustavo
Año de publicación
2005
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
This study aimed to explore the signaling pathways involved in the positive inotropic effect (PIE) of low doses of endothelin-1 (ET-1). Cat papillary muscles were used for force and intracellular Na+ concentration (Na+i) measurements, and isolated cat ventricular myocytes for patch-clamp experiments. ET-1 (5 nmol/L) induced a PIE and an associated increase in Na+i that were abolished by Na +/H+ exchanger (NHE) inhibition with HOE642. Reverse-mode Na+/Ca2+ exchanger (NCX) blockade with KB-R7943 reversed the ET-1-induced PIE. These results suggest that the ET-1-induced PIE is totally attributable to the NHE-mediated Na+i increase. However, an additional direct stimulating effect of ET-1 on NCX after the necessary increase in Na+i could occur. Thus, the ET-1-induced increase in Na+i and contractility was compared with that induced by partial inhibition of the Na+/K+ ATPase by lowering extracellular K+ (K+o) For a given Na+i, ET-1 induced a greater PIE than low K+o. In the presence of HOE642 and after increasing contractility and Na+i by low K+o, ET-1 induced an additional PIE that was reversed by KB-R7943 or the protein kinase C (PKC) inhibitor chelerythrine. ET-1 increased the NCX current and negatively shifted the NCX reversal potential (ENCX). HOE642 attenuated the increase in NCX outward current and abolished the ENCX shift. These results indicate that whereas the NHE-mediated ET-1-induced increase in Na+i seems to be mandatory to drive NCX in reverse and enhance contractility, Na+i-independent and PKC-dependent NCX stimulation appears to additionally contribute to the PIE. However, it is important to stress that the latter can only occur after the primary participation of the former.
Facultad de Ciencias Médicas
Centro de Investigaciones Cardiovasculares
Materia
Ciencias Médicas
Contraction
Endothelin
Ion channels
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/84302

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/84302
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathwaysAiello, Ernesto AlejandroVilla Abrille, María CelesteDulce, Raúl ArielCingolani, Horacio EugenioPérez, Néstor GustavoCiencias MédicasContractionEndothelinIon channelsThis study aimed to explore the signaling pathways involved in the positive inotropic effect (PIE) of low doses of endothelin-1 (ET-1). Cat papillary muscles were used for force and intracellular Na<SUP>+</SUP> concentration (Na<SUP>+</SUP><SUB>i</SUB>) measurements, and isolated cat ventricular myocytes for patch-clamp experiments. ET-1 (5 nmol/L) induced a PIE and an associated increase in Na<SUP>+</SUP><SUB>i</SUB> that were abolished by Na +/H+ exchanger (NHE) inhibition with HOE642. Reverse-mode Na<SUP>+</SUP>/Ca<SUP>2+</SUP> exchanger (NCX) blockade with KB-R7943 reversed the ET-1-induced PIE. These results suggest that the ET-1-induced PIE is totally attributable to the NHE-mediated Na<SUP>+</SUP><SUB>i</SUB> increase. However, an additional direct stimulating effect of ET-1 on NCX after the necessary increase in Na<SUP>+</SUP><SUB>i</SUB> could occur. Thus, the ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> and contractility was compared with that induced by partial inhibition of the Na<SUP>+</SUP>/K<SUP>+</SUP> ATPase by lowering extracellular K<SUP>+</SUP> (K<SUP>+</SUP><SUB>o</SUB>) For a given Na<SUP>+</SUP><SUB>i</SUB>, ET-1 induced a greater PIE than low K<SUP>+</SUP><SUB>o</SUB>. In the presence of HOE642 and after increasing contractility and Na<SUP>+</SUP><SUB>i</SUB> by low K<SUP>+</SUP><SUB>o</SUB>, ET-1 induced an additional PIE that was reversed by KB-R7943 or the protein kinase C (PKC) inhibitor chelerythrine. ET-1 increased the NCX current and negatively shifted the NCX reversal potential (E<SUB>NCX</SUB>). HOE642 attenuated the increase in NCX outward current and abolished the E<SUB>NCX</SUB> shift. These results indicate that whereas the NHE-mediated ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> seems to be mandatory to drive NCX in reverse and enhance contractility, Na<SUP>+</SUP><SUB>i</SUB>-independent and PKC-dependent NCX stimulation appears to additionally contribute to the PIE. However, it is important to stress that the latter can only occur after the primary participation of the former.Facultad de Ciencias MédicasCentro de Investigaciones Cardiovasculares2005info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf288-293http://sedici.unlp.edu.ar/handle/10915/84302enginfo:eu-repo/semantics/altIdentifier/issn/0194-911Xinfo:eu-repo/semantics/altIdentifier/doi/10.1161/01.HYP.0000152700.58940.b2info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:16:14Zoai:sedici.unlp.edu.ar:10915/84302Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:16:15.283SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
title Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
spellingShingle Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
Aiello, Ernesto Alejandro
Ciencias Médicas
Contraction
Endothelin
Ion channels
title_short Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
title_full Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
title_fullStr Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
title_full_unstemmed Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
title_sort Endothelin-1 stimulates the Na+/Ca2+ exchanger reverse mode through intracellular Na+ (Na+i) - Dependent and Na+i-independent pathways
dc.creator.none.fl_str_mv Aiello, Ernesto Alejandro
Villa Abrille, María Celeste
Dulce, Raúl Ariel
Cingolani, Horacio Eugenio
Pérez, Néstor Gustavo
author Aiello, Ernesto Alejandro
author_facet Aiello, Ernesto Alejandro
Villa Abrille, María Celeste
Dulce, Raúl Ariel
Cingolani, Horacio Eugenio
Pérez, Néstor Gustavo
author_role author
author2 Villa Abrille, María Celeste
Dulce, Raúl Ariel
Cingolani, Horacio Eugenio
Pérez, Néstor Gustavo
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Médicas
Contraction
Endothelin
Ion channels
topic Ciencias Médicas
Contraction
Endothelin
Ion channels
dc.description.none.fl_txt_mv This study aimed to explore the signaling pathways involved in the positive inotropic effect (PIE) of low doses of endothelin-1 (ET-1). Cat papillary muscles were used for force and intracellular Na<SUP>+</SUP> concentration (Na<SUP>+</SUP><SUB>i</SUB>) measurements, and isolated cat ventricular myocytes for patch-clamp experiments. ET-1 (5 nmol/L) induced a PIE and an associated increase in Na<SUP>+</SUP><SUB>i</SUB> that were abolished by Na +/H+ exchanger (NHE) inhibition with HOE642. Reverse-mode Na<SUP>+</SUP>/Ca<SUP>2+</SUP> exchanger (NCX) blockade with KB-R7943 reversed the ET-1-induced PIE. These results suggest that the ET-1-induced PIE is totally attributable to the NHE-mediated Na<SUP>+</SUP><SUB>i</SUB> increase. However, an additional direct stimulating effect of ET-1 on NCX after the necessary increase in Na<SUP>+</SUP><SUB>i</SUB> could occur. Thus, the ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> and contractility was compared with that induced by partial inhibition of the Na<SUP>+</SUP>/K<SUP>+</SUP> ATPase by lowering extracellular K<SUP>+</SUP> (K<SUP>+</SUP><SUB>o</SUB>) For a given Na<SUP>+</SUP><SUB>i</SUB>, ET-1 induced a greater PIE than low K<SUP>+</SUP><SUB>o</SUB>. In the presence of HOE642 and after increasing contractility and Na<SUP>+</SUP><SUB>i</SUB> by low K<SUP>+</SUP><SUB>o</SUB>, ET-1 induced an additional PIE that was reversed by KB-R7943 or the protein kinase C (PKC) inhibitor chelerythrine. ET-1 increased the NCX current and negatively shifted the NCX reversal potential (E<SUB>NCX</SUB>). HOE642 attenuated the increase in NCX outward current and abolished the E<SUB>NCX</SUB> shift. These results indicate that whereas the NHE-mediated ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> seems to be mandatory to drive NCX in reverse and enhance contractility, Na<SUP>+</SUP><SUB>i</SUB>-independent and PKC-dependent NCX stimulation appears to additionally contribute to the PIE. However, it is important to stress that the latter can only occur after the primary participation of the former.
Facultad de Ciencias Médicas
Centro de Investigaciones Cardiovasculares
description This study aimed to explore the signaling pathways involved in the positive inotropic effect (PIE) of low doses of endothelin-1 (ET-1). Cat papillary muscles were used for force and intracellular Na<SUP>+</SUP> concentration (Na<SUP>+</SUP><SUB>i</SUB>) measurements, and isolated cat ventricular myocytes for patch-clamp experiments. ET-1 (5 nmol/L) induced a PIE and an associated increase in Na<SUP>+</SUP><SUB>i</SUB> that were abolished by Na +/H+ exchanger (NHE) inhibition with HOE642. Reverse-mode Na<SUP>+</SUP>/Ca<SUP>2+</SUP> exchanger (NCX) blockade with KB-R7943 reversed the ET-1-induced PIE. These results suggest that the ET-1-induced PIE is totally attributable to the NHE-mediated Na<SUP>+</SUP><SUB>i</SUB> increase. However, an additional direct stimulating effect of ET-1 on NCX after the necessary increase in Na<SUP>+</SUP><SUB>i</SUB> could occur. Thus, the ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> and contractility was compared with that induced by partial inhibition of the Na<SUP>+</SUP>/K<SUP>+</SUP> ATPase by lowering extracellular K<SUP>+</SUP> (K<SUP>+</SUP><SUB>o</SUB>) For a given Na<SUP>+</SUP><SUB>i</SUB>, ET-1 induced a greater PIE than low K<SUP>+</SUP><SUB>o</SUB>. In the presence of HOE642 and after increasing contractility and Na<SUP>+</SUP><SUB>i</SUB> by low K<SUP>+</SUP><SUB>o</SUB>, ET-1 induced an additional PIE that was reversed by KB-R7943 or the protein kinase C (PKC) inhibitor chelerythrine. ET-1 increased the NCX current and negatively shifted the NCX reversal potential (E<SUB>NCX</SUB>). HOE642 attenuated the increase in NCX outward current and abolished the E<SUB>NCX</SUB> shift. These results indicate that whereas the NHE-mediated ET-1-induced increase in Na<SUP>+</SUP><SUB>i</SUB> seems to be mandatory to drive NCX in reverse and enhance contractility, Na<SUP>+</SUP><SUB>i</SUB>-independent and PKC-dependent NCX stimulation appears to additionally contribute to the PIE. However, it is important to stress that the latter can only occur after the primary participation of the former.
publishDate 2005
dc.date.none.fl_str_mv 2005
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/84302
url http://sedici.unlp.edu.ar/handle/10915/84302
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0194-911X
info:eu-repo/semantics/altIdentifier/doi/10.1161/01.HYP.0000152700.58940.b2
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
288-293
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