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
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/139365

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network_name_str SEDICI (UNLP)
spelling 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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instname:Universidad Nacional de La Plata
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reponame_str SEDICI (UNLP)
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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