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Molecular hydrogen increases resilience to stress in mice

The inability to successfully adapt to stress produces pathological changes that can lead to depression. Molecular hydrogen has anti-oxidative and anti-inflammatory activities and neuroprotective effects. However, the potential role of molecular hydrogen in stress-related disorders is still poorly u...

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Autores principales: Gao, Qiang, Song, Han, Wang, Xiao-ting, Liang, Ying, Xi, Yan-jie, Gao, Yuan, Guo, Qing-jun, LeBaron, Tyler, Luo, Yi-xiao, Li, Shuang-cheng, Yin, Xi, Shi, Hai-shui, Ma, Yu-xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575246/
https://www.ncbi.nlm.nih.gov/pubmed/28852144
http://dx.doi.org/10.1038/s41598-017-10362-6
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author Gao, Qiang
Song, Han
Wang, Xiao-ting
Liang, Ying
Xi, Yan-jie
Gao, Yuan
Guo, Qing-jun
LeBaron, Tyler
Luo, Yi-xiao
Li, Shuang-cheng
Yin, Xi
Shi, Hai-shui
Ma, Yu-xia
author_facet Gao, Qiang
Song, Han
Wang, Xiao-ting
Liang, Ying
Xi, Yan-jie
Gao, Yuan
Guo, Qing-jun
LeBaron, Tyler
Luo, Yi-xiao
Li, Shuang-cheng
Yin, Xi
Shi, Hai-shui
Ma, Yu-xia
author_sort Gao, Qiang
collection PubMed
description The inability to successfully adapt to stress produces pathological changes that can lead to depression. Molecular hydrogen has anti-oxidative and anti-inflammatory activities and neuroprotective effects. However, the potential role of molecular hydrogen in stress-related disorders is still poorly understood. The present study aims to investigate the effects of hydrogen gas on resilience to stress in mice. The results showed that repeated inhalation of hydrogen-oxygen mixed gas [67%:33% (V/V)] significantly decreased both the acute and chronic stress-induced depressive- and anxiety-like behaviors of mice, assessed by tail suspension test (TST), forced swimming test (FST), novelty suppressed feeding (NSF) test, and open field test (OFT). ELISA analyses showed that inhalation of hydrogen-oxygen mixed gas blocked CMS-induced increase in the serum levels of corticosterone, adrenocorticotropic hormone, interleukin-6, and tumor necrosis factor-α in mice exposed to chronic mild stress. Finally, inhalation of hydrogen gas in adolescence significantly increased the resilience to acute stress in early adulthood, which illustrates the long-lasting effects of hydrogen on stress resilience in mice. This was likely mediated by inhibiting the hypothalamic-pituitary-adrenal axis and inflammatory responses to stress. These results warrant further exploration for developing molecular hydrogen as a novel strategy to prevent the occurrence of stress-related disorders.
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spelling pubmed-55752462017-09-01 Molecular hydrogen increases resilience to stress in mice Gao, Qiang Song, Han Wang, Xiao-ting Liang, Ying Xi, Yan-jie Gao, Yuan Guo, Qing-jun LeBaron, Tyler Luo, Yi-xiao Li, Shuang-cheng Yin, Xi Shi, Hai-shui Ma, Yu-xia Sci Rep Article The inability to successfully adapt to stress produces pathological changes that can lead to depression. Molecular hydrogen has anti-oxidative and anti-inflammatory activities and neuroprotective effects. However, the potential role of molecular hydrogen in stress-related disorders is still poorly understood. The present study aims to investigate the effects of hydrogen gas on resilience to stress in mice. The results showed that repeated inhalation of hydrogen-oxygen mixed gas [67%:33% (V/V)] significantly decreased both the acute and chronic stress-induced depressive- and anxiety-like behaviors of mice, assessed by tail suspension test (TST), forced swimming test (FST), novelty suppressed feeding (NSF) test, and open field test (OFT). ELISA analyses showed that inhalation of hydrogen-oxygen mixed gas blocked CMS-induced increase in the serum levels of corticosterone, adrenocorticotropic hormone, interleukin-6, and tumor necrosis factor-α in mice exposed to chronic mild stress. Finally, inhalation of hydrogen gas in adolescence significantly increased the resilience to acute stress in early adulthood, which illustrates the long-lasting effects of hydrogen on stress resilience in mice. This was likely mediated by inhibiting the hypothalamic-pituitary-adrenal axis and inflammatory responses to stress. These results warrant further exploration for developing molecular hydrogen as a novel strategy to prevent the occurrence of stress-related disorders. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575246/ /pubmed/28852144 http://dx.doi.org/10.1038/s41598-017-10362-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gao, Qiang
Song, Han
Wang, Xiao-ting
Liang, Ying
Xi, Yan-jie
Gao, Yuan
Guo, Qing-jun
LeBaron, Tyler
Luo, Yi-xiao
Li, Shuang-cheng
Yin, Xi
Shi, Hai-shui
Ma, Yu-xia
Molecular hydrogen increases resilience to stress in mice
title Molecular hydrogen increases resilience to stress in mice
title_full Molecular hydrogen increases resilience to stress in mice
title_fullStr Molecular hydrogen increases resilience to stress in mice
title_full_unstemmed Molecular hydrogen increases resilience to stress in mice
title_short Molecular hydrogen increases resilience to stress in mice
title_sort molecular hydrogen increases resilience to stress in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575246/
https://www.ncbi.nlm.nih.gov/pubmed/28852144
http://dx.doi.org/10.1038/s41598-017-10362-6
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