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Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia

The present study aims to investigate the impact of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia. Thirty Sprague-Dawley rats were randomly divided into five groups, including normal diet group, and diabetes model (DM) group, DM + metformin treatment (...

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Autores principales: Zhao, Chuan, Guo, Yushu, Wang, Ruoxi, Cheng, Cheng, Chen, Xiangmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552820/
https://www.ncbi.nlm.nih.gov/pubmed/34697262
http://dx.doi.org/10.4196/kjpp.2021.25.6.517
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author Zhao, Chuan
Guo, Yushu
Wang, Ruoxi
Cheng, Cheng
Chen, Xiangmei
author_facet Zhao, Chuan
Guo, Yushu
Wang, Ruoxi
Cheng, Cheng
Chen, Xiangmei
author_sort Zhao, Chuan
collection PubMed
description The present study aims to investigate the impact of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia. Thirty Sprague-Dawley rats were randomly divided into five groups, including normal diet group, and diabetes model (DM) group, DM + metformin treatment (DMM) group, DMM + hypoxia treatment (DMMH) group and DMMH + hydrogen-rich water (DMMHR) group. We found that the levels of lactic acid, pyruvate and lactate dehydrogenase were significantly lower in the blood of DMMHR group than DMMH group. Superoxide dismutase and glutathione levels in liver and heart were significantly higher in DMMH group after hydrogen-rich water treatment, while malondialdehyde and oxidized glutathione levels were decreased in DMMHR group when compared with DMMH group, which indicates that hydrogen-rich water could reduce oxidative stress. qPCR analysis demonstrated that that pro-apoptotic genes Bax/Caspase-3 were upregulated in DM group and metformin treatment suppressed their upregulation (DMM group). However, hypoxic condition reversed the effect of metformin on apoptotic gene expression, and hydrogen-rich water showed little effect on these genes under hypoxia. HE staining showed that hydrogen-rich water prevented myocardial fiber damages under hypoxia. In summary, we conclude that hydrogen-rich water could prevent lactate accumulation and reduce oxidant stress in diabetic rat model to prevent hypoxia-induced damages. It could be served as a potential agent for diabetes patients with metformin treatment to prevent lactic acidosis and reduce myocardial damages under hypoxic conditions.
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spelling pubmed-85528202021-11-10 Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia Zhao, Chuan Guo, Yushu Wang, Ruoxi Cheng, Cheng Chen, Xiangmei Korean J Physiol Pharmacol Original Article The present study aims to investigate the impact of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia. Thirty Sprague-Dawley rats were randomly divided into five groups, including normal diet group, and diabetes model (DM) group, DM + metformin treatment (DMM) group, DMM + hypoxia treatment (DMMH) group and DMMH + hydrogen-rich water (DMMHR) group. We found that the levels of lactic acid, pyruvate and lactate dehydrogenase were significantly lower in the blood of DMMHR group than DMMH group. Superoxide dismutase and glutathione levels in liver and heart were significantly higher in DMMH group after hydrogen-rich water treatment, while malondialdehyde and oxidized glutathione levels were decreased in DMMHR group when compared with DMMH group, which indicates that hydrogen-rich water could reduce oxidative stress. qPCR analysis demonstrated that that pro-apoptotic genes Bax/Caspase-3 were upregulated in DM group and metformin treatment suppressed their upregulation (DMM group). However, hypoxic condition reversed the effect of metformin on apoptotic gene expression, and hydrogen-rich water showed little effect on these genes under hypoxia. HE staining showed that hydrogen-rich water prevented myocardial fiber damages under hypoxia. In summary, we conclude that hydrogen-rich water could prevent lactate accumulation and reduce oxidant stress in diabetic rat model to prevent hypoxia-induced damages. It could be served as a potential agent for diabetes patients with metformin treatment to prevent lactic acidosis and reduce myocardial damages under hypoxic conditions. The Korean Physiological Society and The Korean Society of Pharmacology 2021-11-01 2021-11-01 /pmc/articles/PMC8552820/ /pubmed/34697262 http://dx.doi.org/10.4196/kjpp.2021.25.6.517 Text en Copyright © Korean J Physiol Pharmacol https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zhao, Chuan
Guo, Yushu
Wang, Ruoxi
Cheng, Cheng
Chen, Xiangmei
Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title_full Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title_fullStr Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title_full_unstemmed Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title_short Effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
title_sort effect of hydrogen-rich water on the lactic acid level in metformin-treated diabetic rats under hypoxia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8552820/
https://www.ncbi.nlm.nih.gov/pubmed/34697262
http://dx.doi.org/10.4196/kjpp.2021.25.6.517
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