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The Clinical Application of Hydrogen as a Medical Treatment.

水素の医療応用に関する臨床的考察:多様な投与経路と疾患モデルへの効果

review mixed routes not assessed

Abstract

Molecular hydrogen has demonstrated beneficial effects across a range of disease models, with ischemia-reperfusion injury being among the most studied. Research in this field has expanded rapidly as evidence accumulates. Notably, hydrogen exerts its effects through multiple administration routes—including gaseous inhalation, oral ingestion, intravenous infusion, and topical application—indicating broad versatility. This review consolidates recent findings on hydrogen-rich water and evaluates prospects for its clinical use. Attention has also grown around hydrogen's role as a gaseous signaling molecule capable of modulating oxidative stress pathways, and further mechanistic and clinical investigations are anticipated.

Mechanism

Molecular hydrogen is thought to selectively neutralize reactive oxygen species, particularly hydroxyl radicals, thereby suppressing oxidative stress signaling and conferring cytoprotective effects.

Bibliographic

Authors
Iida A, Nosaka N, Yumoto T, Knaup E, Naito H, Nishiyama C, et al.
Journal
Acta Med Okayama
Year
2016
PMID
27777424
DOI
10.18926/AMO/54590

Tags

Disease:虚血再灌流障害 Delivery:吸入投与 点滴投与 水素水経口投与 Mechanism:ヒドロキシルラジカル消去 酸化ストレス 活性酸素種

Delivery context

This study combines multiple delivery routes. As a general principle, the most efficient route for routine hydrogen intake is inhalation. Inhalation carries explosion risk (empirical LFL of 10%; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

Safety notes

This study combines multiple delivery routes. As a general principle, the most efficient route for routine hydrogen intake is inhalation. Inhalation carries explosion risk (empirical LFL of 10%; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

See also:

Other papers on the same disease / condition

Cite as: H2 Papers — PMID 27777424. https://h2-papers.org/en/papers/27777424
Source: PubMed PMID 27777424