Signal transduction pathways involved in non-genomic action of estrone on vascular tissue
- Autores
- Massheimer, Virginia Laura; Polini, Nélida Nora; Alvarez, Cristina; Benozzi, Silvia; Rauschemberger, María Belén; Sellés, Juana
- Año de publicación
- 2006
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Previously we demonstrated that estrone non-genomically regulates rat aortic NOS and COX activity and that this effect depends on ovarian activity. The purpose of the present study was to characterize this effect and investigate the participation of phospholipase C and phophatidylinositol-3-kinase system in the intracellular transduction pathway involved in the response. Using aortic strips isolated from female fertile rats we showed that estrone stimulate nitric oxide synthase and cyclooxygenase in a short time interval (5-20 min), and that NO production was dependent in part on PGI2 production since 1 μM indomethacin significantly reduced this free radical production. Injection of 17-β-estradiol to ovariectomized rats restored tissue capacity to rapidly increase NO production in response to "in vitro" treatment with 1 nM estrone. We also demonstrated that in aortic strips isolated from intact animals estrone elicited a rapid phospholipase C activation, inducing a biphasic increase in diacylglycerol generation (peaking at 45 s and 5 min). The presence of protein kinase C inhibitor chelerythrine did not prevent the increase of NO released in response to hormone treatment. We proved that PI3K-Akt system does not mediate NOS and COX activation. However, PLC activation was dependent on PI3K since presence of LY 294002 in the incubation medium abolished estrone-induced DAG increment. We concluded that, estrone rapid action on vascular tissue involves a cross talk between NOS and COX system, and the activation of PLC/DAG/PKC transduction pathways.
Fil: Massheimer, Virginia Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Polini, Nélida Nora. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Alvarez, Cristina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Benozzi, Silvia. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Rauschemberger, María Belén. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina
Fil: Sellés, Juana. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina - Materia
-
Cyclooxygenase
Estrone
Nitric Oxide Synthase
Ovarian Hormones
Phospholipase C
Rat Aorta - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/82246
Ver los metadatos del registro completo
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Signal transduction pathways involved in non-genomic action of estrone on vascular tissueMassheimer, Virginia LauraPolini, Nélida NoraAlvarez, CristinaBenozzi, SilviaRauschemberger, María BelénSellés, JuanaCyclooxygenaseEstroneNitric Oxide SynthaseOvarian HormonesPhospholipase CRat Aortahttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Previously we demonstrated that estrone non-genomically regulates rat aortic NOS and COX activity and that this effect depends on ovarian activity. The purpose of the present study was to characterize this effect and investigate the participation of phospholipase C and phophatidylinositol-3-kinase system in the intracellular transduction pathway involved in the response. Using aortic strips isolated from female fertile rats we showed that estrone stimulate nitric oxide synthase and cyclooxygenase in a short time interval (5-20 min), and that NO production was dependent in part on PGI2 production since 1 μM indomethacin significantly reduced this free radical production. Injection of 17-β-estradiol to ovariectomized rats restored tissue capacity to rapidly increase NO production in response to "in vitro" treatment with 1 nM estrone. We also demonstrated that in aortic strips isolated from intact animals estrone elicited a rapid phospholipase C activation, inducing a biphasic increase in diacylglycerol generation (peaking at 45 s and 5 min). The presence of protein kinase C inhibitor chelerythrine did not prevent the increase of NO released in response to hormone treatment. We proved that PI3K-Akt system does not mediate NOS and COX activation. However, PLC activation was dependent on PI3K since presence of LY 294002 in the incubation medium abolished estrone-induced DAG increment. We concluded that, estrone rapid action on vascular tissue involves a cross talk between NOS and COX system, and the activation of PLC/DAG/PKC transduction pathways.Fil: Massheimer, Virginia Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Polini, Nélida Nora. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Alvarez, Cristina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Benozzi, Silvia. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Rauschemberger, María Belén. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; ArgentinaFil: Sellés, Juana. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaElsevier Science Inc2006-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/82246Massheimer, Virginia Laura; Polini, Nélida Nora; Alvarez, Cristina; Benozzi, Silvia; Rauschemberger, María Belén; et al.; Signal transduction pathways involved in non-genomic action of estrone on vascular tissue; Elsevier Science Inc; Steroids; 71; 10; 10-2006; 857-8640039-128XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0039128X06001310info:eu-repo/semantics/altIdentifier/doi/10.1016/j.steroids.2006.05.015info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:06:08Zoai:ri.conicet.gov.ar:11336/82246instacron: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:34982025-10-22 12:06:08.515CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| title |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| spellingShingle |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue Massheimer, Virginia Laura Cyclooxygenase Estrone Nitric Oxide Synthase Ovarian Hormones Phospholipase C Rat Aorta |
| title_short |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| title_full |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| title_fullStr |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| title_full_unstemmed |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| title_sort |
Signal transduction pathways involved in non-genomic action of estrone on vascular tissue |
| dc.creator.none.fl_str_mv |
Massheimer, Virginia Laura Polini, Nélida Nora Alvarez, Cristina Benozzi, Silvia Rauschemberger, María Belén Sellés, Juana |
| author |
Massheimer, Virginia Laura |
| author_facet |
Massheimer, Virginia Laura Polini, Nélida Nora Alvarez, Cristina Benozzi, Silvia Rauschemberger, María Belén Sellés, Juana |
| author_role |
author |
| author2 |
Polini, Nélida Nora Alvarez, Cristina Benozzi, Silvia Rauschemberger, María Belén Sellés, Juana |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
Cyclooxygenase Estrone Nitric Oxide Synthase Ovarian Hormones Phospholipase C Rat Aorta |
| topic |
Cyclooxygenase Estrone Nitric Oxide Synthase Ovarian Hormones Phospholipase C Rat Aorta |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Previously we demonstrated that estrone non-genomically regulates rat aortic NOS and COX activity and that this effect depends on ovarian activity. The purpose of the present study was to characterize this effect and investigate the participation of phospholipase C and phophatidylinositol-3-kinase system in the intracellular transduction pathway involved in the response. Using aortic strips isolated from female fertile rats we showed that estrone stimulate nitric oxide synthase and cyclooxygenase in a short time interval (5-20 min), and that NO production was dependent in part on PGI2 production since 1 μM indomethacin significantly reduced this free radical production. Injection of 17-β-estradiol to ovariectomized rats restored tissue capacity to rapidly increase NO production in response to "in vitro" treatment with 1 nM estrone. We also demonstrated that in aortic strips isolated from intact animals estrone elicited a rapid phospholipase C activation, inducing a biphasic increase in diacylglycerol generation (peaking at 45 s and 5 min). The presence of protein kinase C inhibitor chelerythrine did not prevent the increase of NO released in response to hormone treatment. We proved that PI3K-Akt system does not mediate NOS and COX activation. However, PLC activation was dependent on PI3K since presence of LY 294002 in the incubation medium abolished estrone-induced DAG increment. We concluded that, estrone rapid action on vascular tissue involves a cross talk between NOS and COX system, and the activation of PLC/DAG/PKC transduction pathways. Fil: Massheimer, Virginia Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Polini, Nélida Nora. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Alvarez, Cristina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Benozzi, Silvia. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Rauschemberger, María Belén. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca; Argentina Fil: Sellés, Juana. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina |
| description |
Previously we demonstrated that estrone non-genomically regulates rat aortic NOS and COX activity and that this effect depends on ovarian activity. The purpose of the present study was to characterize this effect and investigate the participation of phospholipase C and phophatidylinositol-3-kinase system in the intracellular transduction pathway involved in the response. Using aortic strips isolated from female fertile rats we showed that estrone stimulate nitric oxide synthase and cyclooxygenase in a short time interval (5-20 min), and that NO production was dependent in part on PGI2 production since 1 μM indomethacin significantly reduced this free radical production. Injection of 17-β-estradiol to ovariectomized rats restored tissue capacity to rapidly increase NO production in response to "in vitro" treatment with 1 nM estrone. We also demonstrated that in aortic strips isolated from intact animals estrone elicited a rapid phospholipase C activation, inducing a biphasic increase in diacylglycerol generation (peaking at 45 s and 5 min). The presence of protein kinase C inhibitor chelerythrine did not prevent the increase of NO released in response to hormone treatment. We proved that PI3K-Akt system does not mediate NOS and COX activation. However, PLC activation was dependent on PI3K since presence of LY 294002 in the incubation medium abolished estrone-induced DAG increment. We concluded that, estrone rapid action on vascular tissue involves a cross talk between NOS and COX system, and the activation of PLC/DAG/PKC transduction pathways. |
| publishDate |
2006 |
| dc.date.none.fl_str_mv |
2006-10 |
| 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 |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/82246 Massheimer, Virginia Laura; Polini, Nélida Nora; Alvarez, Cristina; Benozzi, Silvia; Rauschemberger, María Belén; et al.; Signal transduction pathways involved in non-genomic action of estrone on vascular tissue; Elsevier Science Inc; Steroids; 71; 10; 10-2006; 857-864 0039-128X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/82246 |
| identifier_str_mv |
Massheimer, Virginia Laura; Polini, Nélida Nora; Alvarez, Cristina; Benozzi, Silvia; Rauschemberger, María Belén; et al.; Signal transduction pathways involved in non-genomic action of estrone on vascular tissue; Elsevier Science Inc; Steroids; 71; 10; 10-2006; 857-864 0039-128X CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
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info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0039128X06001310 info:eu-repo/semantics/altIdentifier/doi/10.1016/j.steroids.2006.05.015 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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application/pdf application/pdf application/pdf application/pdf application/pdf |
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Elsevier Science Inc |
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Elsevier Science Inc |
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