Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate
- Autores
- Cutini, Pablo Hernan; Campelo, Adrián Esteban; Massheimer, Virginia Laura
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Medroxyprogesterone acetate (MPA) is a synthetic progestin commonly used in hormone replacement therapy (HRT). The aim of this work was to study and compare the effect of progesterone (Pg) and MPA, on the regulation of cellular events associated with vascular homeostasis and disease. Platelet adhesion to endothelial cells (ECs), nitric oxide (NO) production, and cell migration were studied using murine endothelial cells in vitro exposed to the progestins. After seven minutes treatment, MPA significantly inhibited NO synthesis with respect to control value; meanwhile Pg markedly increased vasoactive production. In senile ECs, the stimulatory action of Pg decreases; meanwhile MPA maintained its ability to inhibit NO synthesis.The presence of RU486 antagonized each steroid action. When ECs were preincubated with PD98059 (MAPK inhibitor) or chelerythrine (PKC inhibitor) before Pg or MPA treatment, the former totally suppressed the steroid action, but the PKC antagonist did not affect NO production. In the presence of a PI3K inhibitor (LY294002) a partial reduction in Pg effect, and a reversal of MPA action was detected. Using indomethacin the contribution of cyclooxygenase (COX) pathway was also detected. On platelet adhesion assays, Pg inhibited and MPA stimulated platelet adhesion to ECs. Under inflammatory conditions, Pg prevented platelet adhesion induced by lipopolysaccharide (LPS); meanwhile MPA potentiated the stimulatory action of LPS. Finally, although both steroids enhanced ECs migration, MPA exhibited a greater effect. In conclusion the data presented in this research provide evidence of a differential regulation of vascular function by Pg and MPA
Fil: Cutini, Pablo Hernan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Campelo, Adrián Esteban. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; Argentina
Fil: Massheimer, Virginia Laura. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; Argentina - Materia
-
Endothelium
Progesterone
Medroxiprogesterone
Vascular - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/7452
Ver los metadatos del registro completo
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Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetateCutini, Pablo HernanCampelo, Adrián EstebanMassheimer, Virginia LauraEndotheliumProgesteroneMedroxiprogesteroneVascularhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Medroxyprogesterone acetate (MPA) is a synthetic progestin commonly used in hormone replacement therapy (HRT). The aim of this work was to study and compare the effect of progesterone (Pg) and MPA, on the regulation of cellular events associated with vascular homeostasis and disease. Platelet adhesion to endothelial cells (ECs), nitric oxide (NO) production, and cell migration were studied using murine endothelial cells in vitro exposed to the progestins. After seven minutes treatment, MPA significantly inhibited NO synthesis with respect to control value; meanwhile Pg markedly increased vasoactive production. In senile ECs, the stimulatory action of Pg decreases; meanwhile MPA maintained its ability to inhibit NO synthesis.The presence of RU486 antagonized each steroid action. When ECs were preincubated with PD98059 (MAPK inhibitor) or chelerythrine (PKC inhibitor) before Pg or MPA treatment, the former totally suppressed the steroid action, but the PKC antagonist did not affect NO production. In the presence of a PI3K inhibitor (LY294002) a partial reduction in Pg effect, and a reversal of MPA action was detected. Using indomethacin the contribution of cyclooxygenase (COX) pathway was also detected. On platelet adhesion assays, Pg inhibited and MPA stimulated platelet adhesion to ECs. Under inflammatory conditions, Pg prevented platelet adhesion induced by lipopolysaccharide (LPS); meanwhile MPA potentiated the stimulatory action of LPS. Finally, although both steroids enhanced ECs migration, MPA exhibited a greater effect. In conclusion the data presented in this research provide evidence of a differential regulation of vascular function by Pg and MPAFil: Cutini, Pablo Hernan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Campelo, Adrián Esteban. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; ArgentinaFil: Massheimer, Virginia Laura. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; ArgentinaBioscientifica2013-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/rarapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/7452Cutini, Pablo Hernan; Campelo, Adrián Esteban; Massheimer, Virginia Laura; Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate; Bioscientifica; Journal Of Endocrinology; 220; 12-2013; 179-1930022-0795enginfo:eu-repo/semantics/altIdentifier/url/http://joe.endocrinology-journals.org/content/220/3/179.longinfo:eu-repo/semantics/altIdentifier/doi/10.1530/JOE-13-0263info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:46:23Zoai:ri.conicet.gov.ar:11336/7452instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:46:24.049CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
title |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
spellingShingle |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate Cutini, Pablo Hernan Endothelium Progesterone Medroxiprogesterone Vascular |
title_short |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
title_full |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
title_fullStr |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
title_full_unstemmed |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
title_sort |
Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate |
dc.creator.none.fl_str_mv |
Cutini, Pablo Hernan Campelo, Adrián Esteban Massheimer, Virginia Laura |
author |
Cutini, Pablo Hernan |
author_facet |
Cutini, Pablo Hernan Campelo, Adrián Esteban Massheimer, Virginia Laura |
author_role |
author |
author2 |
Campelo, Adrián Esteban Massheimer, Virginia Laura |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Endothelium Progesterone Medroxiprogesterone Vascular |
topic |
Endothelium Progesterone Medroxiprogesterone Vascular |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Medroxyprogesterone acetate (MPA) is a synthetic progestin commonly used in hormone replacement therapy (HRT). The aim of this work was to study and compare the effect of progesterone (Pg) and MPA, on the regulation of cellular events associated with vascular homeostasis and disease. Platelet adhesion to endothelial cells (ECs), nitric oxide (NO) production, and cell migration were studied using murine endothelial cells in vitro exposed to the progestins. After seven minutes treatment, MPA significantly inhibited NO synthesis with respect to control value; meanwhile Pg markedly increased vasoactive production. In senile ECs, the stimulatory action of Pg decreases; meanwhile MPA maintained its ability to inhibit NO synthesis.The presence of RU486 antagonized each steroid action. When ECs were preincubated with PD98059 (MAPK inhibitor) or chelerythrine (PKC inhibitor) before Pg or MPA treatment, the former totally suppressed the steroid action, but the PKC antagonist did not affect NO production. In the presence of a PI3K inhibitor (LY294002) a partial reduction in Pg effect, and a reversal of MPA action was detected. Using indomethacin the contribution of cyclooxygenase (COX) pathway was also detected. On platelet adhesion assays, Pg inhibited and MPA stimulated platelet adhesion to ECs. Under inflammatory conditions, Pg prevented platelet adhesion induced by lipopolysaccharide (LPS); meanwhile MPA potentiated the stimulatory action of LPS. Finally, although both steroids enhanced ECs migration, MPA exhibited a greater effect. In conclusion the data presented in this research provide evidence of a differential regulation of vascular function by Pg and MPA Fil: Cutini, Pablo Hernan. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Campelo, Adrián Esteban. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; Argentina Fil: Massheimer, Virginia Laura. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Bahia Blanca; Argentina |
description |
Medroxyprogesterone acetate (MPA) is a synthetic progestin commonly used in hormone replacement therapy (HRT). The aim of this work was to study and compare the effect of progesterone (Pg) and MPA, on the regulation of cellular events associated with vascular homeostasis and disease. Platelet adhesion to endothelial cells (ECs), nitric oxide (NO) production, and cell migration were studied using murine endothelial cells in vitro exposed to the progestins. After seven minutes treatment, MPA significantly inhibited NO synthesis with respect to control value; meanwhile Pg markedly increased vasoactive production. In senile ECs, the stimulatory action of Pg decreases; meanwhile MPA maintained its ability to inhibit NO synthesis.The presence of RU486 antagonized each steroid action. When ECs were preincubated with PD98059 (MAPK inhibitor) or chelerythrine (PKC inhibitor) before Pg or MPA treatment, the former totally suppressed the steroid action, but the PKC antagonist did not affect NO production. In the presence of a PI3K inhibitor (LY294002) a partial reduction in Pg effect, and a reversal of MPA action was detected. Using indomethacin the contribution of cyclooxygenase (COX) pathway was also detected. On platelet adhesion assays, Pg inhibited and MPA stimulated platelet adhesion to ECs. Under inflammatory conditions, Pg prevented platelet adhesion induced by lipopolysaccharide (LPS); meanwhile MPA potentiated the stimulatory action of LPS. Finally, although both steroids enhanced ECs migration, MPA exhibited a greater effect. In conclusion the data presented in this research provide evidence of a differential regulation of vascular function by Pg and MPA |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/11336/7452 Cutini, Pablo Hernan; Campelo, Adrián Esteban; Massheimer, Virginia Laura; Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate; Bioscientifica; Journal Of Endocrinology; 220; 12-2013; 179-193 0022-0795 |
url |
http://hdl.handle.net/11336/7452 |
identifier_str_mv |
Cutini, Pablo Hernan; Campelo, Adrián Esteban; Massheimer, Virginia Laura; Differential regulation of endothelium behavior by progesterone and medroxyprogesterone acetate; Bioscientifica; Journal Of Endocrinology; 220; 12-2013; 179-193 0022-0795 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://joe.endocrinology-journals.org/content/220/3/179.long info:eu-repo/semantics/altIdentifier/doi/10.1530/JOE-13-0263 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/rar application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Bioscientifica |
publisher.none.fl_str_mv |
Bioscientifica |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842268791448272896 |
score |
13.13397 |