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Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction

Intermittent exposure to hypoxia (IHE) increases the production of reactive oxygen and nitrogen species as well as erythropoietin (EPO), which stimulates the adaptation to intense physical activity. However, several studies suggest a protective effect of moderate hypoxia in cardiovascular disease (C...

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Autores principales: Zembron-Lacny, Agnieszka, Tylutka, Anna, Wacka, Eryk, Wawrzyniak-Gramacka, Edyta, Hiczkiewicz, Dariusz, Kasperska, Anna, Czuba, Miłosz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453230/
https://www.ncbi.nlm.nih.gov/pubmed/32923484
http://dx.doi.org/10.1155/2020/6479630
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author Zembron-Lacny, Agnieszka
Tylutka, Anna
Wacka, Eryk
Wawrzyniak-Gramacka, Edyta
Hiczkiewicz, Dariusz
Kasperska, Anna
Czuba, Miłosz
author_facet Zembron-Lacny, Agnieszka
Tylutka, Anna
Wacka, Eryk
Wawrzyniak-Gramacka, Edyta
Hiczkiewicz, Dariusz
Kasperska, Anna
Czuba, Miłosz
author_sort Zembron-Lacny, Agnieszka
collection PubMed
description Intermittent exposure to hypoxia (IHE) increases the production of reactive oxygen and nitrogen species as well as erythropoietin (EPO), which stimulates the adaptation to intense physical activity. However, several studies suggest a protective effect of moderate hypoxia in cardiovascular disease (CVD) events. The effects of intense physical activity with IHE on oxi-inflammatory mediators and their interaction with conventional CVD risk factors were investigated. Blood samples were collected from elite athletes (control n = 6, IHE n = 6) during a 6-day IHE cycle using hypoxicator GO2 altitude. IHE was held once a day, at least 2 hours after training. In serum, hydrogen peroxide (H(2)O(2)), nitric oxide (NO), 3-nitrotyrosine (3-Nitro), proinflammatory cytokines (IL-1β and TNFα), high sensitivity C-reactive protein (hsCRP), and heat shock protein 27 (HSP27) were determined by the commercial immunoenzyme (ELISA kits) or colorimetric methods. Serum erythropoietin (EPO) level was measured by ELISA kit every day of hypoxia. IHE was found to significantly increase H(2)O(2), NO, and HSP27 but to decrease 3NT concentrations. The changes in 3NT and HSP27 following hypoxia proved to enhance NO bioavailability and endothelial function. In the present study, the oxi-inflammatory mediators IL-1β and hsCRP increased in IHE group but they did not exceed the reference values. The serum EPO level increased on the 3(rd) day of IHE, then decreased on 5(th) day of IHE, and correlated with NO/H(2)O(2) ratio (r(s) = 0.640, P < 0.05). There were no changes in haematological markers contrary to lipoproteins such as low-density lipoprotein (LDL) and non-high-density lipoprotein (non-HDL) which showed a decreasing trend in response to hypoxic exposure. The study demonstrated that IHE combined with sports activity reduced a risk of endothelial dysfunction and atherogenesis in athletes even though the oxi-inflammatory processes were enhanced. Therefore, 6-day IHE seems to be a potential therapeutic and nonpharmacological method to reduce CVD risk, especially in elite athletes participating in strenuous training.
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spelling pubmed-74532302020-09-11 Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction Zembron-Lacny, Agnieszka Tylutka, Anna Wacka, Eryk Wawrzyniak-Gramacka, Edyta Hiczkiewicz, Dariusz Kasperska, Anna Czuba, Miłosz Biomed Res Int Research Article Intermittent exposure to hypoxia (IHE) increases the production of reactive oxygen and nitrogen species as well as erythropoietin (EPO), which stimulates the adaptation to intense physical activity. However, several studies suggest a protective effect of moderate hypoxia in cardiovascular disease (CVD) events. The effects of intense physical activity with IHE on oxi-inflammatory mediators and their interaction with conventional CVD risk factors were investigated. Blood samples were collected from elite athletes (control n = 6, IHE n = 6) during a 6-day IHE cycle using hypoxicator GO2 altitude. IHE was held once a day, at least 2 hours after training. In serum, hydrogen peroxide (H(2)O(2)), nitric oxide (NO), 3-nitrotyrosine (3-Nitro), proinflammatory cytokines (IL-1β and TNFα), high sensitivity C-reactive protein (hsCRP), and heat shock protein 27 (HSP27) were determined by the commercial immunoenzyme (ELISA kits) or colorimetric methods. Serum erythropoietin (EPO) level was measured by ELISA kit every day of hypoxia. IHE was found to significantly increase H(2)O(2), NO, and HSP27 but to decrease 3NT concentrations. The changes in 3NT and HSP27 following hypoxia proved to enhance NO bioavailability and endothelial function. In the present study, the oxi-inflammatory mediators IL-1β and hsCRP increased in IHE group but they did not exceed the reference values. The serum EPO level increased on the 3(rd) day of IHE, then decreased on 5(th) day of IHE, and correlated with NO/H(2)O(2) ratio (r(s) = 0.640, P < 0.05). There were no changes in haematological markers contrary to lipoproteins such as low-density lipoprotein (LDL) and non-high-density lipoprotein (non-HDL) which showed a decreasing trend in response to hypoxic exposure. The study demonstrated that IHE combined with sports activity reduced a risk of endothelial dysfunction and atherogenesis in athletes even though the oxi-inflammatory processes were enhanced. Therefore, 6-day IHE seems to be a potential therapeutic and nonpharmacological method to reduce CVD risk, especially in elite athletes participating in strenuous training. Hindawi 2020-08-19 /pmc/articles/PMC7453230/ /pubmed/32923484 http://dx.doi.org/10.1155/2020/6479630 Text en Copyright © 2020 Agnieszka Zembron-Lacny et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zembron-Lacny, Agnieszka
Tylutka, Anna
Wacka, Eryk
Wawrzyniak-Gramacka, Edyta
Hiczkiewicz, Dariusz
Kasperska, Anna
Czuba, Miłosz
Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title_full Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title_fullStr Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title_full_unstemmed Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title_short Intermittent Hypoxic Exposure Reduces Endothelial Dysfunction
title_sort intermittent hypoxic exposure reduces endothelial dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453230/
https://www.ncbi.nlm.nih.gov/pubmed/32923484
http://dx.doi.org/10.1155/2020/6479630
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