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Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects

Objective: Hypoxic exposure can be used as a therapeutic tool by inducing various cardiovascular, neuromuscular, and metabolic adaptations. Hypoxic conditioning strategies have been evaluated in patients with chronic diseases using either sustained (SH) or intermittent (IH) hypoxic sessions. Whether...

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Autores principales: Chacaroun, Samarmar, Borowik, Anna, Morrison, Shawnda A., Baillieul, Sébastien, Flore, Patrice, Doutreleau, Stéphane, Verges, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222853/
https://www.ncbi.nlm.nih.gov/pubmed/28119623
http://dx.doi.org/10.3389/fphys.2016.00675
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author Chacaroun, Samarmar
Borowik, Anna
Morrison, Shawnda A.
Baillieul, Sébastien
Flore, Patrice
Doutreleau, Stéphane
Verges, Samuel
author_facet Chacaroun, Samarmar
Borowik, Anna
Morrison, Shawnda A.
Baillieul, Sébastien
Flore, Patrice
Doutreleau, Stéphane
Verges, Samuel
author_sort Chacaroun, Samarmar
collection PubMed
description Objective: Hypoxic exposure can be used as a therapeutic tool by inducing various cardiovascular, neuromuscular, and metabolic adaptations. Hypoxic conditioning strategies have been evaluated in patients with chronic diseases using either sustained (SH) or intermittent (IH) hypoxic sessions. Whether hypoxic conditioning via SH or IH may induce different physiological responses remains to be elucidated. Methods: Fourteen healthy active subjects (7 females, age 25 ± 8 years, body mass index 21.5 ± 2.5 kg·m(−2)) performed two interventions in a single blind, randomized cross-over design, starting with either 3 x SH (48 h apart), or 3 x IH (48 h apart), separated by a 2 week washout period. SH sessions consisted of breathing a gas mixture with reduced inspiratory oxygen fraction (FiO(2)), continuously adjusted to reach arterial oxygen saturations (SpO(2)) of 70–80% for 1 h. IH sessions consisted of 5 min with reduced FiO(2) (SpO(2) = 70–80%), followed by 3-min normoxia, repeated seven times. During the first (S1) and third (S3) sessions of each hypoxic intervention, cardiorespiratory parameters, and muscle and pre-frontal cortex oxygenation (near infrared spectroscopy) were assessed continuously. Results: Minute ventilation increased significantly during IH sessions (+2 ± 2 L·min(−1)) while heart rate increased during both SH (+11 ± 4 bpm) and IH (+13 ± 5 bpm) sessions. Arterial blood pressure increased during all hypoxic sessions, although baseline normoxic systolic blood pressure was reduced from S1 to S3 in IH only (−8 ± 11 mmHg). Muscle oxygenation decreased significantly during S3 but not S1, for both hypoxic interventions (S3: SH −6 ± 5%, IH −3 ± 4%); pre-frontal oxygenation decreased in S1 and S3, and to a greater extent in SH vs. IH (−13 ± 3% vs. −6 ± 6%). Heart rate variability indices indicated a significantly larger increase in sympathetic activity in SH vs. IH (lower SDNN, PNN50, and RMSSD values in SH). From S1 to S3, further reduction in heart rate variability was observed in SH (SDNN, PNN50, and RMSSD reduction) while heart rate variability increased in IH (SDNN and RMSSD increase). Conclusions: These results showed significant differences in heart rate variability, blood pressure, and tissue oxygenation changes during short-term SH vs. IH conditioning interventions. Heart rate variability may provide useful information about the early adaptations induced by such intervention.
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spelling pubmed-52228532017-01-24 Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects Chacaroun, Samarmar Borowik, Anna Morrison, Shawnda A. Baillieul, Sébastien Flore, Patrice Doutreleau, Stéphane Verges, Samuel Front Physiol Physiology Objective: Hypoxic exposure can be used as a therapeutic tool by inducing various cardiovascular, neuromuscular, and metabolic adaptations. Hypoxic conditioning strategies have been evaluated in patients with chronic diseases using either sustained (SH) or intermittent (IH) hypoxic sessions. Whether hypoxic conditioning via SH or IH may induce different physiological responses remains to be elucidated. Methods: Fourteen healthy active subjects (7 females, age 25 ± 8 years, body mass index 21.5 ± 2.5 kg·m(−2)) performed two interventions in a single blind, randomized cross-over design, starting with either 3 x SH (48 h apart), or 3 x IH (48 h apart), separated by a 2 week washout period. SH sessions consisted of breathing a gas mixture with reduced inspiratory oxygen fraction (FiO(2)), continuously adjusted to reach arterial oxygen saturations (SpO(2)) of 70–80% for 1 h. IH sessions consisted of 5 min with reduced FiO(2) (SpO(2) = 70–80%), followed by 3-min normoxia, repeated seven times. During the first (S1) and third (S3) sessions of each hypoxic intervention, cardiorespiratory parameters, and muscle and pre-frontal cortex oxygenation (near infrared spectroscopy) were assessed continuously. Results: Minute ventilation increased significantly during IH sessions (+2 ± 2 L·min(−1)) while heart rate increased during both SH (+11 ± 4 bpm) and IH (+13 ± 5 bpm) sessions. Arterial blood pressure increased during all hypoxic sessions, although baseline normoxic systolic blood pressure was reduced from S1 to S3 in IH only (−8 ± 11 mmHg). Muscle oxygenation decreased significantly during S3 but not S1, for both hypoxic interventions (S3: SH −6 ± 5%, IH −3 ± 4%); pre-frontal oxygenation decreased in S1 and S3, and to a greater extent in SH vs. IH (−13 ± 3% vs. −6 ± 6%). Heart rate variability indices indicated a significantly larger increase in sympathetic activity in SH vs. IH (lower SDNN, PNN50, and RMSSD values in SH). From S1 to S3, further reduction in heart rate variability was observed in SH (SDNN, PNN50, and RMSSD reduction) while heart rate variability increased in IH (SDNN and RMSSD increase). Conclusions: These results showed significant differences in heart rate variability, blood pressure, and tissue oxygenation changes during short-term SH vs. IH conditioning interventions. Heart rate variability may provide useful information about the early adaptations induced by such intervention. Frontiers Media S.A. 2017-01-10 /pmc/articles/PMC5222853/ /pubmed/28119623 http://dx.doi.org/10.3389/fphys.2016.00675 Text en Copyright © 2017 Chacaroun, Borowik, Morrison, Baillieul, Flore, Doutreleau and Verges. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Chacaroun, Samarmar
Borowik, Anna
Morrison, Shawnda A.
Baillieul, Sébastien
Flore, Patrice
Doutreleau, Stéphane
Verges, Samuel
Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title_full Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title_fullStr Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title_full_unstemmed Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title_short Physiological Responses to Two Hypoxic Conditioning Strategies in Healthy Subjects
title_sort physiological responses to two hypoxic conditioning strategies in healthy subjects
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222853/
https://www.ncbi.nlm.nih.gov/pubmed/28119623
http://dx.doi.org/10.3389/fphys.2016.00675
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