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Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model
BACKGROUND: Hydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage. Oxidative stress and inflammation contribute to the pathogenesis and/or development of pulmonary hypertension. In this study, we investigated the effects...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065415/ https://www.ncbi.nlm.nih.gov/pubmed/21375753 http://dx.doi.org/10.1186/1465-9921-12-26 |
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author | Wang, Yun Jing, Lei Zhao, Xiao-Min Han, Ji-Ju Xia, Zuo-Li Qin, Shu-Cun Wu, Ya-Ping Sun, Xue-Jun |
author_facet | Wang, Yun Jing, Lei Zhao, Xiao-Min Han, Ji-Ju Xia, Zuo-Li Qin, Shu-Cun Wu, Ya-Ping Sun, Xue-Jun |
author_sort | Wang, Yun |
collection | PubMed |
description | BACKGROUND: Hydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage. Oxidative stress and inflammation contribute to the pathogenesis and/or development of pulmonary hypertension. In this study, we investigated the effects of hydrogen-rich saline on the prevention of pulmonary hypertension induced by monocrotaline in a rat model. METHODS: In male Sprague-Dawley rats, pulmonary hypertension was induced by subcutaneous administration of monocrotaline at a concentration of 6 mg/100 g body weight. Hydrogen-rich saline (5 ml/kg) or saline was administred intraperitoneally once daily for 2 or 3 weeks. Severity of pulmonary hypertension was assessed by hemodynamic index and histologic analysis. Malondialdehyde and 8-hydroxy-desoxyguanosine level, and superoxide dismutase activity were measured in the lung tissue and serum. Levels of pro-inflammatory cytokines (tumor necrosis factor-α, interleukin-6) in serum were determined with enzyme-linked immunosorbent assay. RESULTS: Hydrogen-rich saline treatment improved hemodynamics and reversed right ventricular hypertrophy. It also decreased malondialdehyde and 8-hydroxy-desoxyguanosine levels, and increased superoxide dismutase activity in the lung tissue and serum, accompanied by a decrease in pro-inflammatory cytokines. CONCLUSIONS: These results suggest that hydrogen-rich saline ameliorates the progression of pulmonary hypertension induced by monocrotaline in rats, which may be associated with its antioxidant and anti-inflammatory effects. |
format | Text |
id | pubmed-3065415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30654152011-03-29 Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model Wang, Yun Jing, Lei Zhao, Xiao-Min Han, Ji-Ju Xia, Zuo-Li Qin, Shu-Cun Wu, Ya-Ping Sun, Xue-Jun Respir Res Research BACKGROUND: Hydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage. Oxidative stress and inflammation contribute to the pathogenesis and/or development of pulmonary hypertension. In this study, we investigated the effects of hydrogen-rich saline on the prevention of pulmonary hypertension induced by monocrotaline in a rat model. METHODS: In male Sprague-Dawley rats, pulmonary hypertension was induced by subcutaneous administration of monocrotaline at a concentration of 6 mg/100 g body weight. Hydrogen-rich saline (5 ml/kg) or saline was administred intraperitoneally once daily for 2 or 3 weeks. Severity of pulmonary hypertension was assessed by hemodynamic index and histologic analysis. Malondialdehyde and 8-hydroxy-desoxyguanosine level, and superoxide dismutase activity were measured in the lung tissue and serum. Levels of pro-inflammatory cytokines (tumor necrosis factor-α, interleukin-6) in serum were determined with enzyme-linked immunosorbent assay. RESULTS: Hydrogen-rich saline treatment improved hemodynamics and reversed right ventricular hypertrophy. It also decreased malondialdehyde and 8-hydroxy-desoxyguanosine levels, and increased superoxide dismutase activity in the lung tissue and serum, accompanied by a decrease in pro-inflammatory cytokines. CONCLUSIONS: These results suggest that hydrogen-rich saline ameliorates the progression of pulmonary hypertension induced by monocrotaline in rats, which may be associated with its antioxidant and anti-inflammatory effects. BioMed Central 2011 2011-03-04 /pmc/articles/PMC3065415/ /pubmed/21375753 http://dx.doi.org/10.1186/1465-9921-12-26 Text en Copyright ©2011 Wang 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 | Research Wang, Yun Jing, Lei Zhao, Xiao-Min Han, Ji-Ju Xia, Zuo-Li Qin, Shu-Cun Wu, Ya-Ping Sun, Xue-Jun Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title | Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title_full | Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title_fullStr | Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title_full_unstemmed | Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title_short | Protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
title_sort | protective effects of hydrogen-rich saline on monocrotaline-induced pulmonary hypertension in a rat model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065415/ https://www.ncbi.nlm.nih.gov/pubmed/21375753 http://dx.doi.org/10.1186/1465-9921-12-26 |
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