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Effect of hydrogen-rich water on acute peritonitis of rat models.

水素水が急性腹膜炎ラットモデルに与える影響の検討

animal study hydrogen-rich water positive

Abstract

Three distinct rat models of acute peritonitis were established using intraperitoneal lipopolysaccharide (LPS), fecal injection, or cecal ligation and puncture (CLP). Male Sprague-Dawley rats received hydrogen-rich water (HRW, 3 ml per rat) or saline by oral gavage for 7 days before and 3 days after model induction. Across all three models, HRW administration significantly reduced circulating white blood cell counts, plasma endotoxin levels, and pro-inflammatory cytokines IL-6 and TNF-α. In visceral peritoneal tissue, HRW elevated glutathione (GSH) activity while decreasing myeloperoxidase (MPO) and malondialdehyde (MDA) levels. Immunohistochemical analysis revealed suppressed NF-κB expression in peritoneal tissue, and histopathological examination confirmed reduced tissue damage. These findings indicate that HRW attenuates acute peritonitis severity through combined anti-inflammatory, antioxidant, and antibacterial mechanisms.

Mechanism

HRW suppresses NF-κB expression in peritoneal tissue, leading to reduced pro-inflammatory cytokines (IL-6, TNF-α) and oxidative stress markers (MDA, MPO), while enhancing the antioxidant glutathione (GSH), collectively mitigating peritoneal inflammation.

Bibliographic

Authors
Zhang JH, Wu QF, Song SD, Wan Y, Zhang RJ, Tai MH, et al.
Journal
Int Immunopharmacol
Year
2014
PMID
24793096
DOI
10.1016/j.intimp.2014.04.011

Tags

Mechanism:抗酸化酵素 グルタチオン 免疫調節 炎症抑制 脂質過酸化 酸化ストレス 活性酸素種

Delivery context

Hydrogen-rich water is a low-risk delivery route, but the achievable systemic hydrogen dose is bounded. For clinical applications, inhalation is the most efficient route; inhalation, however, carries explosion risk, and concentration matters (empirical LFL of 10% applies to inhalation environments; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

Safety notes

Hydrogen-rich water is a low-risk delivery route, but the achievable systemic hydrogen dose is bounded. For clinical applications, inhalation is the most efficient route; inhalation, however, carries explosion risk, and concentration matters (empirical LFL of 10% applies to inhalation environments; high-concentration devices are documented in the Consumer Affairs Agency accident database and are not recommended).

See also:

Cite as: H2 Papers — PMID 24793096. https://h2-papers.org/en/papers/24793096
Source: PubMed PMID 24793096