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Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats

The aim of the current study was to identify the protective effect of hydrogen gas against liver injury during CO(2) pneumoperitoneum. Rats were randomly divided into three groups: control group (C group), pneumoperitoneum group (P15 group) and hydrogen group (H(2) group). Rats in the C group were s...

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Autores principales: Chen, Mingzi, Jiang, Lihong, Li, Yue, Bai, Ge, Zhao, Jinghua, Zhang, Ming, Zhang, Jiantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788665/
https://www.ncbi.nlm.nih.gov/pubmed/29416797
http://dx.doi.org/10.18632/oncotarget.23498
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author Chen, Mingzi
Jiang, Lihong
Li, Yue
Bai, Ge
Zhao, Jinghua
Zhang, Ming
Zhang, Jiantao
author_facet Chen, Mingzi
Jiang, Lihong
Li, Yue
Bai, Ge
Zhao, Jinghua
Zhang, Ming
Zhang, Jiantao
author_sort Chen, Mingzi
collection PubMed
description The aim of the current study was to identify the protective effect of hydrogen gas against liver injury during CO(2) pneumoperitoneum. Rats were randomly divided into three groups: control group (C group), pneumoperitoneum group (P15 group) and hydrogen group (H(2) group). Rats in the C group were subjected to anesthesia for 90 min. Rats in the P15 group received an abdominal insufflation of CO(2) for 90 min at an intra-abdominal pressure of 15 mmHg. Rats in the H(2) group received a hypodermic injection of hydrogen gas (0.2 mL/kg) and after 10 min they received an abdominal insufflation of CO(2) for 90 min at an intra-abdominal pressure of 15 mmHg. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were measured to evaluate liver function. Malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione (GSH) content were measured to evaluate oxidative stress. Nuclear factor E2-related factor 2 (Nrf2) and Nrf2 downstream target genes, apoptosis-related genes and inflammatory cytokine mRNA and protein expression were detected. Liver injury was detected under the microscope. Our results revealed that liver function, antioxidants content, inflammation and liver injury were improved after hydrogen preconditioning in H(2) group compared with P15 group. Overall, our results revealed that subcutaneous hydrogen injection could exert a protective effect against liver injury during CO(2) pneumoperitoneum through reducing oxidative stress, cell apoptosis and inflammatory cytokines release.
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spelling pubmed-57886652018-02-07 Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats Chen, Mingzi Jiang, Lihong Li, Yue Bai, Ge Zhao, Jinghua Zhang, Ming Zhang, Jiantao Oncotarget Research Paper The aim of the current study was to identify the protective effect of hydrogen gas against liver injury during CO(2) pneumoperitoneum. Rats were randomly divided into three groups: control group (C group), pneumoperitoneum group (P15 group) and hydrogen group (H(2) group). Rats in the C group were subjected to anesthesia for 90 min. Rats in the P15 group received an abdominal insufflation of CO(2) for 90 min at an intra-abdominal pressure of 15 mmHg. Rats in the H(2) group received a hypodermic injection of hydrogen gas (0.2 mL/kg) and after 10 min they received an abdominal insufflation of CO(2) for 90 min at an intra-abdominal pressure of 15 mmHg. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were measured to evaluate liver function. Malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione (GSH) content were measured to evaluate oxidative stress. Nuclear factor E2-related factor 2 (Nrf2) and Nrf2 downstream target genes, apoptosis-related genes and inflammatory cytokine mRNA and protein expression were detected. Liver injury was detected under the microscope. Our results revealed that liver function, antioxidants content, inflammation and liver injury were improved after hydrogen preconditioning in H(2) group compared with P15 group. Overall, our results revealed that subcutaneous hydrogen injection could exert a protective effect against liver injury during CO(2) pneumoperitoneum through reducing oxidative stress, cell apoptosis and inflammatory cytokines release. Impact Journals LLC 2017-12-15 /pmc/articles/PMC5788665/ /pubmed/29416797 http://dx.doi.org/10.18632/oncotarget.23498 Text en Copyright: © 2018 Chen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Chen, Mingzi
Jiang, Lihong
Li, Yue
Bai, Ge
Zhao, Jinghua
Zhang, Ming
Zhang, Jiantao
Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title_full Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title_fullStr Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title_full_unstemmed Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title_short Hydrogen protects against liver injury during CO(2) pneumoperitoneum in rats
title_sort hydrogen protects against liver injury during co(2) pneumoperitoneum in rats
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788665/
https://www.ncbi.nlm.nih.gov/pubmed/29416797
http://dx.doi.org/10.18632/oncotarget.23498
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