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Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity
BACKGROUND: Oxidative stress (OS) related to glucose degradation products such as methylglyoxal is reportedly associated with peritoneal deterioration in patients treated with peritoneal dialysis (PD). However, the use of general antioxidant agents is limited due to their harmful effects. This study...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734057/ https://www.ncbi.nlm.nih.gov/pubmed/23816239 http://dx.doi.org/10.1186/2045-9912-3-14 |
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author | Terawaki, Hiroyuki Hayashi, Yoshimitsu Zhu, Wan-Jun Matsuyama, Yukie Terada, Tomoyoshi Kabayama, Shigeru Watanabe, Tsuyoshi Era, Seiichi Sato, Bunpei Nakayama, Masaaki |
author_facet | Terawaki, Hiroyuki Hayashi, Yoshimitsu Zhu, Wan-Jun Matsuyama, Yukie Terada, Tomoyoshi Kabayama, Shigeru Watanabe, Tsuyoshi Era, Seiichi Sato, Bunpei Nakayama, Masaaki |
author_sort | Terawaki, Hiroyuki |
collection | PubMed |
description | BACKGROUND: Oxidative stress (OS) related to glucose degradation products such as methylglyoxal is reportedly associated with peritoneal deterioration in patients treated with peritoneal dialysis (PD). However, the use of general antioxidant agents is limited due to their harmful effects. This study aimed to clarify the influence of the novel antioxidant molecular hydrogen (H(2)) on peritoneal OS using albumin redox state as a marker. METHODS: Effluent and blood samples of 6 regular PD patients were obtained during the peritoneal equilibrium test using standard dialysate and hydrogen-enriched dialysate. The redox state of albumin in effluent and blood was determined using high-performance liquid chromatography. RESULTS: Mean proportion of reduced albumin (ƒ(HMA)) in effluent was significantly higher in H(2)-enriched dialysate (62.31 ± 11.10%) than in standard dialysate (54.70 ± 13.08%). Likewise, serum ƒ(HMA) after administration of hydrogen-enriched dialysate (65.75 ± 7.52%) was significantly higher than that after standard dialysate (62.44 ± 7.66%). CONCLUSIONS: Trans-peritoneal administration of H(2) reduces peritoneal and systemic OS. |
format | Online Article Text |
id | pubmed-3734057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37340572013-08-06 Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity Terawaki, Hiroyuki Hayashi, Yoshimitsu Zhu, Wan-Jun Matsuyama, Yukie Terada, Tomoyoshi Kabayama, Shigeru Watanabe, Tsuyoshi Era, Seiichi Sato, Bunpei Nakayama, Masaaki Med Gas Res Research BACKGROUND: Oxidative stress (OS) related to glucose degradation products such as methylglyoxal is reportedly associated with peritoneal deterioration in patients treated with peritoneal dialysis (PD). However, the use of general antioxidant agents is limited due to their harmful effects. This study aimed to clarify the influence of the novel antioxidant molecular hydrogen (H(2)) on peritoneal OS using albumin redox state as a marker. METHODS: Effluent and blood samples of 6 regular PD patients were obtained during the peritoneal equilibrium test using standard dialysate and hydrogen-enriched dialysate. The redox state of albumin in effluent and blood was determined using high-performance liquid chromatography. RESULTS: Mean proportion of reduced albumin (ƒ(HMA)) in effluent was significantly higher in H(2)-enriched dialysate (62.31 ± 11.10%) than in standard dialysate (54.70 ± 13.08%). Likewise, serum ƒ(HMA) after administration of hydrogen-enriched dialysate (65.75 ± 7.52%) was significantly higher than that after standard dialysate (62.44 ± 7.66%). CONCLUSIONS: Trans-peritoneal administration of H(2) reduces peritoneal and systemic OS. BioMed Central 2013-07-01 /pmc/articles/PMC3734057/ /pubmed/23816239 http://dx.doi.org/10.1186/2045-9912-3-14 Text en Copyright © 2013 Terawaki et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Terawaki, Hiroyuki Hayashi, Yoshimitsu Zhu, Wan-Jun Matsuyama, Yukie Terada, Tomoyoshi Kabayama, Shigeru Watanabe, Tsuyoshi Era, Seiichi Sato, Bunpei Nakayama, Masaaki Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title | Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title_full | Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title_fullStr | Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title_full_unstemmed | Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title_short | Transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
title_sort | transperitoneal administration of dissolved hydrogen for peritoneal dialysis patients: a novel approach to suppress oxidative stress in the peritoneal cavity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734057/ https://www.ncbi.nlm.nih.gov/pubmed/23816239 http://dx.doi.org/10.1186/2045-9912-3-14 |
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