Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa

Autores
Lembo, Carina; Renna, Nicolas Federico; Diez, Emiliano Raúl; Vázquez Prieto, Marcela; Miatello, Roberto Miguel
Año de publicación
2010
Idioma
español castellano
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.
Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.
Fil: Lembo, Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Renna, Nicolas Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina
Fil: Diez, Emiliano Raúl. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Vázquez Prieto, Marcela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Miatello, Roberto Miguel. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Materia
Endothelial progenitor cells
Systolic blood pressure
Metabolic syndrome
Fructose-fed hypertensive rats
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/80580

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network_name_str CONICET Digital (CONICET)
spelling Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosaLembo, CarinaRenna, Nicolas FedericoDiez, Emiliano RaúlVázquez Prieto, MarcelaMiatello, Roberto MiguelEndothelial progenitor cellsSystolic blood pressureMetabolic syndromeFructose-fed hypertensive ratshttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.Fil: Lembo, Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Renna, Nicolas Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; ArgentinaFil: Diez, Emiliano Raúl. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Vázquez Prieto, Marcela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Miatello, Roberto Miguel. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaUniversidad Nacional de Cuyo. Facultad de Ciencias Médicas2010-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/80580Lembo, Carina; Renna, Nicolas Federico; Diez, Emiliano Raúl; Vázquez Prieto, Marcela; Miatello, Roberto Miguel; Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa; Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Revista Médica Universitaria; 6; 4; 12-2010; 1-181669-8991CONICET DigitalCONICETspainfo:eu-repo/semantics/altIdentifier/url/http://bdigital.uncu.edu.ar/app/navegador/?idobjeto=3898info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:32Zoai:ri.conicet.gov.ar:11336/80580instacron: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 09:47:32.883CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
title Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
spellingShingle Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
Lembo, Carina
Endothelial progenitor cells
Systolic blood pressure
Metabolic syndrome
Fructose-fed hypertensive rats
title_short Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
title_full Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
title_fullStr Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
title_full_unstemmed Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
title_sort Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa
dc.creator.none.fl_str_mv Lembo, Carina
Renna, Nicolas Federico
Diez, Emiliano Raúl
Vázquez Prieto, Marcela
Miatello, Roberto Miguel
author Lembo, Carina
author_facet Lembo, Carina
Renna, Nicolas Federico
Diez, Emiliano Raúl
Vázquez Prieto, Marcela
Miatello, Roberto Miguel
author_role author
author2 Renna, Nicolas Federico
Diez, Emiliano Raúl
Vázquez Prieto, Marcela
Miatello, Roberto Miguel
author2_role author
author
author
author
dc.subject.none.fl_str_mv Endothelial progenitor cells
Systolic blood pressure
Metabolic syndrome
Fructose-fed hypertensive rats
topic Endothelial progenitor cells
Systolic blood pressure
Metabolic syndrome
Fructose-fed hypertensive rats
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.
Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.
Fil: Lembo, Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Renna, Nicolas Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina
Fil: Diez, Emiliano Raúl. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Vázquez Prieto, Marcela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
Fil: Miatello, Roberto Miguel. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; Argentina
description Objective: To examine alterations in participation of endothelial progenitor cells (EPC) because of insulin resistance (IR) associated with an experimental model of metabolic syndrome (MS) generated by chronic administration of fructose to spontaneously hypertensive rats (SHR) Material and methods: WKY and SHR rats, male, were distributed into 4 groups (n = 8 c/u): WKY: control; FFR: WKY receiving fructose in drinking water to 10% (v/v) for 6 weeks , SHR; FFHR: SHR receiving fructose in drinking water to 10% (v/v) for 6 weeks. At the end of the protocol the following variables were determined: systolic blood pressure, biochemical variables, HOMA index, levels of EPC quantified by flow cytometry in peripheral blood and bone marrow, immunofluorescence in cell culture to identify markers CD34 and VEGFR-2, EPC colony count and NAD(P)H-oxidase activity in aortic tissue. Results: We confirmed the experimental model based on metabolic variables analyzed. A decrease in the levels of CPE, in peripheral blood and bone marrow, which becomes more important groups of animals treated with fructose was observed .In these groups there are also fewer colonies of developed EPC in cell culture and exhibit an increased levels of oxidative stress, estimated by the activity of NAD(P)H-oxidase. Conclusion: the SM caused by chronic administration of fructose in FFHR has proven to generate a decrease in the levels of CPE, as well as its functional capacity. The intracellular mechanisms that produce this phenomenon could be triggered by the degree of IR presented in this experimental model.
publishDate 2010
dc.date.none.fl_str_mv 2010-12
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/11336/80580
Lembo, Carina; Renna, Nicolas Federico; Diez, Emiliano Raúl; Vázquez Prieto, Marcela; Miatello, Roberto Miguel; Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa; Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Revista Médica Universitaria; 6; 4; 12-2010; 1-18
1669-8991
CONICET Digital
CONICET
url http://hdl.handle.net/11336/80580
identifier_str_mv Lembo, Carina; Renna, Nicolas Federico; Diez, Emiliano Raúl; Vázquez Prieto, Marcela; Miatello, Roberto Miguel; Caracterización y cuantificación de células progenitoras endoteliales de ratas espontáneamente hipertensas alimentadas con fructosa; Universidad Nacional de Cuyo. Facultad de Ciencias Médicas; Revista Médica Universitaria; 6; 4; 12-2010; 1-18
1669-8991
CONICET Digital
CONICET
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language spa
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://bdigital.uncu.edu.ar/app/navegador/?idobjeto=3898
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
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rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
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dc.publisher.none.fl_str_mv Universidad Nacional de Cuyo. Facultad de Ciencias Médicas
publisher.none.fl_str_mv Universidad Nacional de Cuyo. Facultad de Ciencias Médicas
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reponame_str CONICET Digital (CONICET)
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repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
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