Potassium channels in human umbilical artery cells
- Autores
- Milesi, María Verónica; Raingo, Jesica; Rebolledo, Alejandro; Grassi de Gende, Ángela Ofelia
- Año de publicación
- 2003
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- To identify K+ channels of smooth muscle of human umbilical artery using the patch-clamp technique and to study their effect on resting tone of umbilical artery rings. Whole-cell and single-channel patch-clamp recordings in enzymatically isolated smooth muscle cells were made. Measurements of developed isometric force were performed on intact tissue. Delayed rectifier K+ channels (KDR) and large-conductance Ca2+-activated K+ channels (BKCa) contribute to the whole-cell voltage-and time-dependent outward K+ current, as it was specifically inhibited by 5 mM 4-aminopyridine (4-AP; KDR blocker) (92 ± 4% at 0 mV, n = 7), by 1 mM tetraethylammonium (TEA; BKCa blocker) (71 ± 4% at +60 mV, n = 4), and by 200 nM iberiotoxin (BKCa blocker) (64 ± 7% at +60 mV, n = 4). In outside-out patches, BKCa channels had ā single-channel conductance of 132 ± 4 pS (n = 24) in asymmetric K+ conditions and 216 ± 4 pS (n = 4) in a symmetric K+ gradient. The activity of the BKCa channels was significantly augmented by 1 μM Ca2+ in the inside-out configuration. 4-AP had no effect on resting tone of intact arterial rings. TEA produced contraction of arterial rings whereas phloretin, an activator of BKCa, relaxed them, which means that BKCa channels are functional in intact tissue and are involved in the maintenance of resting tone in this human vessel. The identities of K+ channels in the human umbilical artery were shown using the patch-clamp technique, and the physiologic effect of K+ channels on resting tone was documented.
Facultad de Ciencias Exactas - Materia
-
Biología
Medicina
BKCa currents
KDR currents
human umbilical artery
smooth muscle cells - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/139365
Ver los metadatos del registro completo
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Potassium channels in human umbilical artery cellsMilesi, María VerónicaRaingo, JesicaRebolledo, AlejandroGrassi de Gende, Ángela OfeliaBiologíaMedicinaBKCa currentsKDR currentshuman umbilical arterysmooth muscle cellsTo identify K+ channels of smooth muscle of human umbilical artery using the patch-clamp technique and to study their effect on resting tone of umbilical artery rings. Whole-cell and single-channel patch-clamp recordings in enzymatically isolated smooth muscle cells were made. Measurements of developed isometric force were performed on intact tissue. Delayed rectifier K+ channels (KDR) and large-conductance Ca2+-activated K+ channels (BKCa) contribute to the whole-cell voltage-and time-dependent outward K+ current, as it was specifically inhibited by 5 mM 4-aminopyridine (4-AP; KDR blocker) (92 ± 4% at 0 mV, n = 7), by 1 mM tetraethylammonium (TEA; BKCa blocker) (71 ± 4% at +60 mV, n = 4), and by 200 nM iberiotoxin (BKCa blocker) (64 ± 7% at +60 mV, n = 4). In outside-out patches, BKCa channels had ā single-channel conductance of 132 ± 4 pS (n = 24) in asymmetric K+ conditions and 216 ± 4 pS (n = 4) in a symmetric K+ gradient. The activity of the BKCa channels was significantly augmented by 1 μM Ca2+ in the inside-out configuration. 4-AP had no effect on resting tone of intact arterial rings. TEA produced contraction of arterial rings whereas phloretin, an activator of BKCa, relaxed them, which means that BKCa channels are functional in intact tissue and are involved in the maintenance of resting tone in this human vessel. The identities of K+ channels in the human umbilical artery were shown using the patch-clamp technique, and the physiologic effect of K+ channels on resting tone was documented.Facultad de Ciencias Exactas2003info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf339-346http://sedici.unlp.edu.ar/handle/10915/139365enginfo:eu-repo/semantics/altIdentifier/issn/1071-5576info:eu-repo/semantics/altIdentifier/issn/1556-7117info:eu-repo/semantics/altIdentifier/pmid/12969776info: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:UNLP2025-10-15T11:23:52Zoai:sedici.unlp.edu.ar:10915/139365Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:23:53.085SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Potassium channels in human umbilical artery cells |
title |
Potassium channels in human umbilical artery cells |
spellingShingle |
Potassium channels in human umbilical artery cells Milesi, María Verónica Biología Medicina BKCa currents KDR currents human umbilical artery smooth muscle cells |
title_short |
Potassium channels in human umbilical artery cells |
title_full |
Potassium channels in human umbilical artery cells |
title_fullStr |
Potassium channels in human umbilical artery cells |
title_full_unstemmed |
Potassium channels in human umbilical artery cells |
title_sort |
Potassium channels in human umbilical artery cells |
dc.creator.none.fl_str_mv |
Milesi, María Verónica Raingo, Jesica Rebolledo, Alejandro Grassi de Gende, Ángela Ofelia |
author |
Milesi, María Verónica |
author_facet |
Milesi, María Verónica Raingo, Jesica Rebolledo, Alejandro Grassi de Gende, Ángela Ofelia |
author_role |
author |
author2 |
Raingo, Jesica Rebolledo, Alejandro Grassi de Gende, Ángela Ofelia |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Biología Medicina BKCa currents KDR currents human umbilical artery smooth muscle cells |
topic |
Biología Medicina BKCa currents KDR currents human umbilical artery smooth muscle cells |
dc.description.none.fl_txt_mv |
To identify K+ channels of smooth muscle of human umbilical artery using the patch-clamp technique and to study their effect on resting tone of umbilical artery rings. Whole-cell and single-channel patch-clamp recordings in enzymatically isolated smooth muscle cells were made. Measurements of developed isometric force were performed on intact tissue. Delayed rectifier K+ channels (KDR) and large-conductance Ca2+-activated K+ channels (BKCa) contribute to the whole-cell voltage-and time-dependent outward K+ current, as it was specifically inhibited by 5 mM 4-aminopyridine (4-AP; KDR blocker) (92 ± 4% at 0 mV, n = 7), by 1 mM tetraethylammonium (TEA; BKCa blocker) (71 ± 4% at +60 mV, n = 4), and by 200 nM iberiotoxin (BKCa blocker) (64 ± 7% at +60 mV, n = 4). In outside-out patches, BKCa channels had ā single-channel conductance of 132 ± 4 pS (n = 24) in asymmetric K+ conditions and 216 ± 4 pS (n = 4) in a symmetric K+ gradient. The activity of the BKCa channels was significantly augmented by 1 μM Ca2+ in the inside-out configuration. 4-AP had no effect on resting tone of intact arterial rings. TEA produced contraction of arterial rings whereas phloretin, an activator of BKCa, relaxed them, which means that BKCa channels are functional in intact tissue and are involved in the maintenance of resting tone in this human vessel. The identities of K+ channels in the human umbilical artery were shown using the patch-clamp technique, and the physiologic effect of K+ channels on resting tone was documented. Facultad de Ciencias Exactas |
description |
To identify K+ channels of smooth muscle of human umbilical artery using the patch-clamp technique and to study their effect on resting tone of umbilical artery rings. Whole-cell and single-channel patch-clamp recordings in enzymatically isolated smooth muscle cells were made. Measurements of developed isometric force were performed on intact tissue. Delayed rectifier K+ channels (KDR) and large-conductance Ca2+-activated K+ channels (BKCa) contribute to the whole-cell voltage-and time-dependent outward K+ current, as it was specifically inhibited by 5 mM 4-aminopyridine (4-AP; KDR blocker) (92 ± 4% at 0 mV, n = 7), by 1 mM tetraethylammonium (TEA; BKCa blocker) (71 ± 4% at +60 mV, n = 4), and by 200 nM iberiotoxin (BKCa blocker) (64 ± 7% at +60 mV, n = 4). In outside-out patches, BKCa channels had ā single-channel conductance of 132 ± 4 pS (n = 24) in asymmetric K+ conditions and 216 ± 4 pS (n = 4) in a symmetric K+ gradient. The activity of the BKCa channels was significantly augmented by 1 μM Ca2+ in the inside-out configuration. 4-AP had no effect on resting tone of intact arterial rings. TEA produced contraction of arterial rings whereas phloretin, an activator of BKCa, relaxed them, which means that BKCa channels are functional in intact tissue and are involved in the maintenance of resting tone in this human vessel. The identities of K+ channels in the human umbilical artery were shown using the patch-clamp technique, and the physiologic effect of K+ channels on resting tone was documented. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003 |
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/10915/139365 |
url |
http://sedici.unlp.edu.ar/handle/10915/139365 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/1071-5576 info:eu-repo/semantics/altIdentifier/issn/1556-7117 info:eu-repo/semantics/altIdentifier/pmid/12969776 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
dc.format.none.fl_str_mv |
application/pdf 339-346 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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