Cargando…
Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion
BACKGROUND: Patients with mesenteric ischemia frequently suffer from bowel necrosis even after revascularization. Hydrogen gas has showed promising effects for ischemia-reperfusion injury by reducing reactive oxygen species in various animal and clinical studies. We examined intestinal tissue injury...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827576/ https://www.ncbi.nlm.nih.gov/pubmed/36632117 http://dx.doi.org/10.4240/wjgs.v14.i12.1329 |
_version_ | 1784867082632953856 |
---|---|
author | Yamamoto, Ryo Suzuki, Sayuri Homma, Koichiro Yamaguchi, Shintaro Sujino, Tomohisa Sasaki, Junichi |
author_facet | Yamamoto, Ryo Suzuki, Sayuri Homma, Koichiro Yamaguchi, Shintaro Sujino, Tomohisa Sasaki, Junichi |
author_sort | Yamamoto, Ryo |
collection | PubMed |
description | BACKGROUND: Patients with mesenteric ischemia frequently suffer from bowel necrosis even after revascularization. Hydrogen gas has showed promising effects for ischemia-reperfusion injury by reducing reactive oxygen species in various animal and clinical studies. We examined intestinal tissue injury by ischemia and reperfusion under continuous initiation of 3% hydrogen gas. AIM: To clarify the treatment effects and target cells of hydrogen gas for mesenteric ischemia. METHODS: Three rat groups underwent 60-min mesenteric artery occlusion (ischemia), 60-min reperfusion following 60-min occlusion (reperfusion), or ischemia-reperfusion with the same duration under continuous 3% hydrogen gas inhalation (hydrogen). The distal ileum was harvested. Immunofluorescence staining with caspase-3 and leucine-rich repeat-containing G-protein-coupled 5 (LGR5), a specific marker of intestinal stem cell, was conducted to evaluate the injury location and cell types protected by hydrogen. mRNA expressions of LGR5, olfactomedin 4 (OLFM4), hairy and enhancer of split 1, Jagged 2, and Neurogenic locus notch homolog protein 1 were measured by quantitative polymerase chain reaction. Tissue oxidative stress was analyzed with immunostaining for 8-hydroxy-2'-deoxyguanosine (8-OHdG). Systemic oxidative stress was evaluated by plasma 8-OHdG. RESULTS: Ischemia damaged the epithelial layer at the tip of the villi, whereas reperfusion induced extensive apoptosis of the cells at the crypt base, which were identified as intestinal stem cells with double immunofluorescence stain. Hydrogen mitigated such apoptosis at the crypt base, and the LGR5 expression of the tissues was higher in the hydrogen group than in the reperfusion group. OLFM4 was also relatively higher in the hydrogen group, whereas other measured RNAs were comparable between the groups. 8-OHdG concentration was high in the reperfusion group, which was reduced by hydrogen, particularly at the crypt base. Serum 8-OHdG concentrations were relatively higher in both reperfusion and hydrogen groups without significance. CONCLUSION: This study demonstrated that hydrogen gas inhalation preserves intestinal stem cells and mitigates oxidative stress caused by mesenteric ischemia and reperfusion. |
format | Online Article Text |
id | pubmed-9827576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-98275762023-01-10 Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion Yamamoto, Ryo Suzuki, Sayuri Homma, Koichiro Yamaguchi, Shintaro Sujino, Tomohisa Sasaki, Junichi World J Gastrointest Surg Basic Study BACKGROUND: Patients with mesenteric ischemia frequently suffer from bowel necrosis even after revascularization. Hydrogen gas has showed promising effects for ischemia-reperfusion injury by reducing reactive oxygen species in various animal and clinical studies. We examined intestinal tissue injury by ischemia and reperfusion under continuous initiation of 3% hydrogen gas. AIM: To clarify the treatment effects and target cells of hydrogen gas for mesenteric ischemia. METHODS: Three rat groups underwent 60-min mesenteric artery occlusion (ischemia), 60-min reperfusion following 60-min occlusion (reperfusion), or ischemia-reperfusion with the same duration under continuous 3% hydrogen gas inhalation (hydrogen). The distal ileum was harvested. Immunofluorescence staining with caspase-3 and leucine-rich repeat-containing G-protein-coupled 5 (LGR5), a specific marker of intestinal stem cell, was conducted to evaluate the injury location and cell types protected by hydrogen. mRNA expressions of LGR5, olfactomedin 4 (OLFM4), hairy and enhancer of split 1, Jagged 2, and Neurogenic locus notch homolog protein 1 were measured by quantitative polymerase chain reaction. Tissue oxidative stress was analyzed with immunostaining for 8-hydroxy-2'-deoxyguanosine (8-OHdG). Systemic oxidative stress was evaluated by plasma 8-OHdG. RESULTS: Ischemia damaged the epithelial layer at the tip of the villi, whereas reperfusion induced extensive apoptosis of the cells at the crypt base, which were identified as intestinal stem cells with double immunofluorescence stain. Hydrogen mitigated such apoptosis at the crypt base, and the LGR5 expression of the tissues was higher in the hydrogen group than in the reperfusion group. OLFM4 was also relatively higher in the hydrogen group, whereas other measured RNAs were comparable between the groups. 8-OHdG concentration was high in the reperfusion group, which was reduced by hydrogen, particularly at the crypt base. Serum 8-OHdG concentrations were relatively higher in both reperfusion and hydrogen groups without significance. CONCLUSION: This study demonstrated that hydrogen gas inhalation preserves intestinal stem cells and mitigates oxidative stress caused by mesenteric ischemia and reperfusion. Baishideng Publishing Group Inc 2022-12-27 2022-12-27 /pmc/articles/PMC9827576/ /pubmed/36632117 http://dx.doi.org/10.4240/wjgs.v14.i12.1329 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Basic Study Yamamoto, Ryo Suzuki, Sayuri Homma, Koichiro Yamaguchi, Shintaro Sujino, Tomohisa Sasaki, Junichi Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title | Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title_full | Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title_fullStr | Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title_full_unstemmed | Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title_short | Hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
title_sort | hydrogen gas and preservation of intestinal stem cells in mesenteric ischemia and reperfusion |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827576/ https://www.ncbi.nlm.nih.gov/pubmed/36632117 http://dx.doi.org/10.4240/wjgs.v14.i12.1329 |
work_keys_str_mv | AT yamamotoryo hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion AT suzukisayuri hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion AT hommakoichiro hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion AT yamaguchishintaro hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion AT sujinotomohisa hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion AT sasakijunichi hydrogengasandpreservationofintestinalstemcellsinmesentericischemiaandreperfusion |