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
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/84302
Ver los metadatos del registro completo
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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 |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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