Cargando…

Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress

Mitochondria are the largest source of reactive oxygen species (ROS) and are intracellular organelles that produce large amounts of the most potent hydroxyl radical (·OH). Molecular hydrogen (H(2)) can selectively eliminate ·OH generated inside of the mitochondria. Inflammation is induced by the rel...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirano, Shin-ichi, Ichikawa, Yusuke, Sato, Bunpei, Yamamoto, Haru, Takefuji, Yoshiyasu, Satoh, Fumitake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961517/
https://www.ncbi.nlm.nih.gov/pubmed/33806292
http://dx.doi.org/10.3390/ijms22052549
_version_ 1783665277579296768
author Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Yamamoto, Haru
Takefuji, Yoshiyasu
Satoh, Fumitake
author_facet Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Yamamoto, Haru
Takefuji, Yoshiyasu
Satoh, Fumitake
author_sort Hirano, Shin-ichi
collection PubMed
description Mitochondria are the largest source of reactive oxygen species (ROS) and are intracellular organelles that produce large amounts of the most potent hydroxyl radical (·OH). Molecular hydrogen (H(2)) can selectively eliminate ·OH generated inside of the mitochondria. Inflammation is induced by the release of proinflammatory cytokines produced by macrophages and neutrophils. However, an uncontrolled or exaggerated response often occurs, resulting in severe inflammation that can lead to acute or chronic inflammatory diseases. Recent studies have reported that ROS activate NLRP3 inflammasomes, and that this stimulation triggers the production of proinflammatory cytokines. It has been shown in literature that H(2) can be based on the mechanisms that inhibit mitochondrial ROS. However, the ability for H(2) to inhibit NLRP3 inflammasome activation via mitochondrial oxidation is poorly understood. In this review, we hypothesize a possible mechanism by which H(2) inhibits mitochondrial oxidation. Medical applications of H(2) may solve the problem of many chronic inflammation-based diseases, including coronavirus disease 2019 (COVID-19).
format Online
Article
Text
id pubmed-7961517
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-79615172021-03-17 Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress Hirano, Shin-ichi Ichikawa, Yusuke Sato, Bunpei Yamamoto, Haru Takefuji, Yoshiyasu Satoh, Fumitake Int J Mol Sci Review Mitochondria are the largest source of reactive oxygen species (ROS) and are intracellular organelles that produce large amounts of the most potent hydroxyl radical (·OH). Molecular hydrogen (H(2)) can selectively eliminate ·OH generated inside of the mitochondria. Inflammation is induced by the release of proinflammatory cytokines produced by macrophages and neutrophils. However, an uncontrolled or exaggerated response often occurs, resulting in severe inflammation that can lead to acute or chronic inflammatory diseases. Recent studies have reported that ROS activate NLRP3 inflammasomes, and that this stimulation triggers the production of proinflammatory cytokines. It has been shown in literature that H(2) can be based on the mechanisms that inhibit mitochondrial ROS. However, the ability for H(2) to inhibit NLRP3 inflammasome activation via mitochondrial oxidation is poorly understood. In this review, we hypothesize a possible mechanism by which H(2) inhibits mitochondrial oxidation. Medical applications of H(2) may solve the problem of many chronic inflammation-based diseases, including coronavirus disease 2019 (COVID-19). MDPI 2021-03-04 /pmc/articles/PMC7961517/ /pubmed/33806292 http://dx.doi.org/10.3390/ijms22052549 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hirano, Shin-ichi
Ichikawa, Yusuke
Sato, Bunpei
Yamamoto, Haru
Takefuji, Yoshiyasu
Satoh, Fumitake
Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title_full Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title_fullStr Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title_full_unstemmed Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title_short Potential Therapeutic Applications of Hydrogen in Chronic Inflammatory Diseases: Possible Inhibiting Role on Mitochondrial Stress
title_sort potential therapeutic applications of hydrogen in chronic inflammatory diseases: possible inhibiting role on mitochondrial stress
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961517/
https://www.ncbi.nlm.nih.gov/pubmed/33806292
http://dx.doi.org/10.3390/ijms22052549
work_keys_str_mv AT hiranoshinichi potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress
AT ichikawayusuke potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress
AT satobunpei potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress
AT yamamotoharu potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress
AT takefujiyoshiyasu potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress
AT satohfumitake potentialtherapeuticapplicationsofhydrogeninchronicinflammatorydiseasespossibleinhibitingroleonmitochondrialstress