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Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats

BACKGROUND: The purpose of the study is to investigate the role and mechanisms of hydrogen-saturated saline (HSS) in the acute lung injury (ALI) induced by oleic acid (OA) in rats. METHODS: Rats were treated with OA (0.1 mL/kg) to induce ALI and then administered with HSS (5 mL/kg) by intravenous (i...

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Autores principales: Ying, Youguo, Xu, Haizhou, Yao, Min, Qin, Zonghe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606060/
https://www.ncbi.nlm.nih.gov/pubmed/28927460
http://dx.doi.org/10.1186/s13018-017-0633-9
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author Ying, Youguo
Xu, Haizhou
Yao, Min
Qin, Zonghe
author_facet Ying, Youguo
Xu, Haizhou
Yao, Min
Qin, Zonghe
author_sort Ying, Youguo
collection PubMed
description BACKGROUND: The purpose of the study is to investigate the role and mechanisms of hydrogen-saturated saline (HSS) in the acute lung injury (ALI) induced by oleic acid (OA) in rats. METHODS: Rats were treated with OA (0.1 mL/kg) to induce ALI and then administered with HSS (5 mL/kg) by intravenous (iv) and intraperitoneal (ip) injection, respectively. Three hours after the injection with OA, the arterial oxygen partial pressure (PaO(2)), arterial oxygen saturation (SaO(2)), carbon dioxide partial pressure (PaCO(2)), and bicarbonate (HCO(3) (−)) levels were analyzed using blood gas analyzer. In addition, the levels of malondialdehyde (MDA), tumor necrosis factor-α (TNF-α), and interleukin 1β (IL-1β) and myeloperoxidase (MPO) activity were measured by commercial kits, and pathological changes of lung tissue were examined by HE staining. Finally, the correlations of MPO activity or MDA level with the levels of TNF-α or IL-1β were analyzed by Pearson’s correlation analysis. RESULTS: We found decreased PaO(2) levels and the pathological changes of lung tissue of ALI after OA injection. In addition, OA increased the levels of MDA, TNF-α, and IL-1β, as well as MPO activity in lung tissues (P < 0.05). However, after treatment with HSS, all of these changes were alleviated (P < 0.05), and these changes were mitigated when treated with HSS by ip then iv injection (P < 0.05). Furthermore, MDA level and MPO activity were positively correlated with TNF-α and IL-1β levels in the lung tissue, respectively (P < 0.01). CONCLUSION: HSS attenuated ALI induced by OA in rats and might protect against ALI through selective resistance to oxidation and inhibiting inflammatory infiltration.
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spelling pubmed-56060602017-09-20 Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats Ying, Youguo Xu, Haizhou Yao, Min Qin, Zonghe J Orthop Surg Res Research Article BACKGROUND: The purpose of the study is to investigate the role and mechanisms of hydrogen-saturated saline (HSS) in the acute lung injury (ALI) induced by oleic acid (OA) in rats. METHODS: Rats were treated with OA (0.1 mL/kg) to induce ALI and then administered with HSS (5 mL/kg) by intravenous (iv) and intraperitoneal (ip) injection, respectively. Three hours after the injection with OA, the arterial oxygen partial pressure (PaO(2)), arterial oxygen saturation (SaO(2)), carbon dioxide partial pressure (PaCO(2)), and bicarbonate (HCO(3) (−)) levels were analyzed using blood gas analyzer. In addition, the levels of malondialdehyde (MDA), tumor necrosis factor-α (TNF-α), and interleukin 1β (IL-1β) and myeloperoxidase (MPO) activity were measured by commercial kits, and pathological changes of lung tissue were examined by HE staining. Finally, the correlations of MPO activity or MDA level with the levels of TNF-α or IL-1β were analyzed by Pearson’s correlation analysis. RESULTS: We found decreased PaO(2) levels and the pathological changes of lung tissue of ALI after OA injection. In addition, OA increased the levels of MDA, TNF-α, and IL-1β, as well as MPO activity in lung tissues (P < 0.05). However, after treatment with HSS, all of these changes were alleviated (P < 0.05), and these changes were mitigated when treated with HSS by ip then iv injection (P < 0.05). Furthermore, MDA level and MPO activity were positively correlated with TNF-α and IL-1β levels in the lung tissue, respectively (P < 0.01). CONCLUSION: HSS attenuated ALI induced by OA in rats and might protect against ALI through selective resistance to oxidation and inhibiting inflammatory infiltration. BioMed Central 2017-09-19 /pmc/articles/PMC5606060/ /pubmed/28927460 http://dx.doi.org/10.1186/s13018-017-0633-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ying, Youguo
Xu, Haizhou
Yao, Min
Qin, Zonghe
Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title_full Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title_fullStr Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title_full_unstemmed Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title_short Protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
title_sort protective effect of hydrogen-saturated saline on acute lung injury induced by oleic acid in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606060/
https://www.ncbi.nlm.nih.gov/pubmed/28927460
http://dx.doi.org/10.1186/s13018-017-0633-9
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