Cargando…

Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease

As diabetes rates surge globally, there is a corresponding rise in the number of patients suffering from diabetic kidney disease (DKD), a common complication of diabetes. DKD is a significant contributor to chronic kidney disease, often leading to end-stage renal failure. However, the effectiveness...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirano, Shin-ichi, Ichikawa, Yusuke, Sato, Bunpei, Takefuji, Yoshiyasu, Satoh, Fumitake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603947/
https://www.ncbi.nlm.nih.gov/pubmed/37893190
http://dx.doi.org/10.3390/biomedicines11102817
_version_ 1785126718022877184
author Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Takefuji, Yoshiyasu
Satoh, Fumitake
author_facet Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Takefuji, Yoshiyasu
Satoh, Fumitake
author_sort Hirano, Shin-ichi
collection PubMed
description As diabetes rates surge globally, there is a corresponding rise in the number of patients suffering from diabetic kidney disease (DKD), a common complication of diabetes. DKD is a significant contributor to chronic kidney disease, often leading to end-stage renal failure. However, the effectiveness of current medical treatments for DKD leaves much to be desired. Molecular hydrogen (H(2)) is an antioxidant that selectively reduces hydroxyl radicals, a reactive oxygen species with a very potent oxidative capacity. Recent studies have demonstrated that H(2) not only possesses antioxidant properties but also exhibits anti-inflammatory effects, regulates cell lethality, and modulates signal transduction. Consequently, it is now being utilized in clinical applications. Many factors contribute to the onset and progression of DKD, with mitochondrial dysfunction, oxidative stress, and inflammation being strongly implicated. Recent preclinical and clinical trials reported that substances with antioxidant properties may slow the progression of DKD. Hence, we undertook a comprehensive review of the literature focusing on animal models and human clinical trials where H(2) demonstrated effectiveness against a variety of renal diseases. The collective evidence from this literature review, along with our previous findings, suggests that H(2) may have therapeutic benefits for patients with DKD by enhancing mitochondrial function. To substantiate these findings, future large-scale clinical studies are needed.
format Online
Article
Text
id pubmed-10603947
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106039472023-10-28 Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease Hirano, Shin-ichi Ichikawa, Yusuke Sato, Bunpei Takefuji, Yoshiyasu Satoh, Fumitake Biomedicines Review As diabetes rates surge globally, there is a corresponding rise in the number of patients suffering from diabetic kidney disease (DKD), a common complication of diabetes. DKD is a significant contributor to chronic kidney disease, often leading to end-stage renal failure. However, the effectiveness of current medical treatments for DKD leaves much to be desired. Molecular hydrogen (H(2)) is an antioxidant that selectively reduces hydroxyl radicals, a reactive oxygen species with a very potent oxidative capacity. Recent studies have demonstrated that H(2) not only possesses antioxidant properties but also exhibits anti-inflammatory effects, regulates cell lethality, and modulates signal transduction. Consequently, it is now being utilized in clinical applications. Many factors contribute to the onset and progression of DKD, with mitochondrial dysfunction, oxidative stress, and inflammation being strongly implicated. Recent preclinical and clinical trials reported that substances with antioxidant properties may slow the progression of DKD. Hence, we undertook a comprehensive review of the literature focusing on animal models and human clinical trials where H(2) demonstrated effectiveness against a variety of renal diseases. The collective evidence from this literature review, along with our previous findings, suggests that H(2) may have therapeutic benefits for patients with DKD by enhancing mitochondrial function. To substantiate these findings, future large-scale clinical studies are needed. MDPI 2023-10-17 /pmc/articles/PMC10603947/ /pubmed/37893190 http://dx.doi.org/10.3390/biomedicines11102817 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Takefuji, Yoshiyasu
Satoh, Fumitake
Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title_full Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title_fullStr Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title_full_unstemmed Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title_short Clinical Use and Treatment Mechanism of Molecular Hydrogen in the Treatment of Various Kidney Diseases including Diabetic Kidney Disease
title_sort clinical use and treatment mechanism of molecular hydrogen in the treatment of various kidney diseases including diabetic kidney disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603947/
https://www.ncbi.nlm.nih.gov/pubmed/37893190
http://dx.doi.org/10.3390/biomedicines11102817
work_keys_str_mv AT hiranoshinichi clinicaluseandtreatmentmechanismofmolecularhydrogeninthetreatmentofvariouskidneydiseasesincludingdiabetickidneydisease
AT ichikawayusuke clinicaluseandtreatmentmechanismofmolecularhydrogeninthetreatmentofvariouskidneydiseasesincludingdiabetickidneydisease
AT satobunpei clinicaluseandtreatmentmechanismofmolecularhydrogeninthetreatmentofvariouskidneydiseasesincludingdiabetickidneydisease
AT takefujiyoshiyasu clinicaluseandtreatmentmechanismofmolecularhydrogeninthetreatmentofvariouskidneydiseasesincludingdiabetickidneydisease
AT satohfumitake clinicaluseandtreatmentmechanismofmolecularhydrogeninthetreatmentofvariouskidneydiseasesincludingdiabetickidneydisease