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Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration

BACKGROUND: Our goal was to determine whether short-term intermittent hypoxia exposure, at a level well tolerated by healthy humans and previously shown by our group to increase EPO and erythropoiesis, could mobilize hematopoietic stem cells (HSC) and increase their presence in peripheral circulatio...

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Autores principales: Viscor, Ginés, Javierre, Casimiro, Pagès, Teresa, Ventura, Josep-Lluis, Ricart, Antoni, Martin-Henao, Gregorio, Azqueta, Carmen, Segura, Ramon
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774674/
https://www.ncbi.nlm.nih.gov/pubmed/19874615
http://dx.doi.org/10.1186/1479-5876-7-91
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author Viscor, Ginés
Javierre, Casimiro
Pagès, Teresa
Ventura, Josep-Lluis
Ricart, Antoni
Martin-Henao, Gregorio
Azqueta, Carmen
Segura, Ramon
author_facet Viscor, Ginés
Javierre, Casimiro
Pagès, Teresa
Ventura, Josep-Lluis
Ricart, Antoni
Martin-Henao, Gregorio
Azqueta, Carmen
Segura, Ramon
author_sort Viscor, Ginés
collection PubMed
description BACKGROUND: Our goal was to determine whether short-term intermittent hypoxia exposure, at a level well tolerated by healthy humans and previously shown by our group to increase EPO and erythropoiesis, could mobilize hematopoietic stem cells (HSC) and increase their presence in peripheral circulation. METHODS: Four healthy male subjects were subjected to three different protocols: one with only a hypoxic stimulus (OH), another with a hypoxic stimulus plus muscle electrostimulation (HME) and the third with only muscle electrostimulation (OME). Intermittent hypobaric hypoxia exposure consisted of only three sessions of three hours at barometric pressure 540 hPa (equivalent to an altitude of 5000 m) for three consecutive days, whereas muscular electrostimulation was performed in two separate periods of 25 min in each session. Blood samples were obtained from an antecubital vein on three consecutive days immediately before the experiment and 24 h, 48 h, 4 days and 7 days after the last day of hypoxic exposure. RESULTS: There was a clear increase in the number of circulating CD34+ cells after combined hypobaric hypoxia and muscular electrostimulation. This response was not observed after the isolated application of the same stimuli. CONCLUSION: Our results open a new application field for hypobaric systems as a way to increase efficiency in peripheral HSC collection.
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spelling pubmed-27746742009-11-10 Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration Viscor, Ginés Javierre, Casimiro Pagès, Teresa Ventura, Josep-Lluis Ricart, Antoni Martin-Henao, Gregorio Azqueta, Carmen Segura, Ramon J Transl Med Methodology BACKGROUND: Our goal was to determine whether short-term intermittent hypoxia exposure, at a level well tolerated by healthy humans and previously shown by our group to increase EPO and erythropoiesis, could mobilize hematopoietic stem cells (HSC) and increase their presence in peripheral circulation. METHODS: Four healthy male subjects were subjected to three different protocols: one with only a hypoxic stimulus (OH), another with a hypoxic stimulus plus muscle electrostimulation (HME) and the third with only muscle electrostimulation (OME). Intermittent hypobaric hypoxia exposure consisted of only three sessions of three hours at barometric pressure 540 hPa (equivalent to an altitude of 5000 m) for three consecutive days, whereas muscular electrostimulation was performed in two separate periods of 25 min in each session. Blood samples were obtained from an antecubital vein on three consecutive days immediately before the experiment and 24 h, 48 h, 4 days and 7 days after the last day of hypoxic exposure. RESULTS: There was a clear increase in the number of circulating CD34+ cells after combined hypobaric hypoxia and muscular electrostimulation. This response was not observed after the isolated application of the same stimuli. CONCLUSION: Our results open a new application field for hypobaric systems as a way to increase efficiency in peripheral HSC collection. BioMed Central 2009-10-29 /pmc/articles/PMC2774674/ /pubmed/19874615 http://dx.doi.org/10.1186/1479-5876-7-91 Text en Copyright © 2009 Viscor et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Viscor, Ginés
Javierre, Casimiro
Pagès, Teresa
Ventura, Josep-Lluis
Ricart, Antoni
Martin-Henao, Gregorio
Azqueta, Carmen
Segura, Ramon
Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title_full Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title_fullStr Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title_full_unstemmed Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title_short Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
title_sort combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774674/
https://www.ncbi.nlm.nih.gov/pubmed/19874615
http://dx.doi.org/10.1186/1479-5876-7-91
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