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Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice

BACKGROUND: Molecular hydrogen (H(2)) has been recognized as an effective antioxidant with no or little side effects. While it is known that oxidative stress is closely associated with aging, the beneficial effect of H(2) on oxidative stress-related aging is still unclear. In this study, a mouse mod...

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Autores principales: Liu, Boyan, Xie, Yunbo, Chen, Jun, Xue, Junli, Zhang, Xiaoyi, Zhao, Min, Jia, Xiubin, Wang, Yiwei, Qin, Shucun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558637/
https://www.ncbi.nlm.nih.gov/pubmed/34737603
http://dx.doi.org/10.2147/JIR.S332286
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author Liu, Boyan
Xie, Yunbo
Chen, Jun
Xue, Junli
Zhang, Xiaoyi
Zhao, Min
Jia, Xiubin
Wang, Yiwei
Qin, Shucun
author_facet Liu, Boyan
Xie, Yunbo
Chen, Jun
Xue, Junli
Zhang, Xiaoyi
Zhao, Min
Jia, Xiubin
Wang, Yiwei
Qin, Shucun
author_sort Liu, Boyan
collection PubMed
description BACKGROUND: Molecular hydrogen (H(2)) has been recognized as an effective antioxidant with no or little side effects. While it is known that oxidative stress is closely associated with aging, the beneficial effect of H(2) on oxidative stress-related aging is still unclear. In this study, a mouse model of D-galactose-induced aging was employed to investigate the protective effects of H(2). METHODS: The mice were administrated of H(2) via different routes (4% H(2) inhalation, H(2)-rich water drinking, and H(2)-rich saline injection), the aging-related biomarkers in plasma and the oxidative stress in different tissues were measured. RESULTS: The results showed that H(2) improved aging-related biomarkers, ie, total antioxidant capacity, advanced glycation end products, tumor necrosis factor-α, free fatty acids, and alanine aminotransferase in plasma. Furthermore, H(2) alleviated oxidative stress in the liver, brain, and heart by reducing the levels of lipid peroxidation and malondialdehyde and increasing the activity of superoxide dismutase. In addition, it seems that 4% H(2) inhalation was the most effective regarding the amount of H(2) taken up and in reducing the markers of oxidative stress in some of the tissues; however, the other routes of administration resulted in the same efficacy in most indicators. CONCLUSION: H(2) can prevent oxidative stress in D-galactose-induced aging mice when administered by different routes.
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spelling pubmed-85586372021-11-03 Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice Liu, Boyan Xie, Yunbo Chen, Jun Xue, Junli Zhang, Xiaoyi Zhao, Min Jia, Xiubin Wang, Yiwei Qin, Shucun J Inflamm Res Original Research BACKGROUND: Molecular hydrogen (H(2)) has been recognized as an effective antioxidant with no or little side effects. While it is known that oxidative stress is closely associated with aging, the beneficial effect of H(2) on oxidative stress-related aging is still unclear. In this study, a mouse model of D-galactose-induced aging was employed to investigate the protective effects of H(2). METHODS: The mice were administrated of H(2) via different routes (4% H(2) inhalation, H(2)-rich water drinking, and H(2)-rich saline injection), the aging-related biomarkers in plasma and the oxidative stress in different tissues were measured. RESULTS: The results showed that H(2) improved aging-related biomarkers, ie, total antioxidant capacity, advanced glycation end products, tumor necrosis factor-α, free fatty acids, and alanine aminotransferase in plasma. Furthermore, H(2) alleviated oxidative stress in the liver, brain, and heart by reducing the levels of lipid peroxidation and malondialdehyde and increasing the activity of superoxide dismutase. In addition, it seems that 4% H(2) inhalation was the most effective regarding the amount of H(2) taken up and in reducing the markers of oxidative stress in some of the tissues; however, the other routes of administration resulted in the same efficacy in most indicators. CONCLUSION: H(2) can prevent oxidative stress in D-galactose-induced aging mice when administered by different routes. Dove 2021-10-27 /pmc/articles/PMC8558637/ /pubmed/34737603 http://dx.doi.org/10.2147/JIR.S332286 Text en © 2021 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Boyan
Xie, Yunbo
Chen, Jun
Xue, Junli
Zhang, Xiaoyi
Zhao, Min
Jia, Xiubin
Wang, Yiwei
Qin, Shucun
Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title_full Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title_fullStr Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title_full_unstemmed Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title_short Protective Effect of Molecular Hydrogen Following Different Routes of Administration on D-Galactose-Induced Aging Mice
title_sort protective effect of molecular hydrogen following different routes of administration on d-galactose-induced aging mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8558637/
https://www.ncbi.nlm.nih.gov/pubmed/34737603
http://dx.doi.org/10.2147/JIR.S332286
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