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Molecular hydrogen decelerates rheumatoid arthritis progression through inhibition of oxidative stress

Meng J, Yu P, Jiang H, Yuan T, Liu N, Tong J, Chen H, Bao N, Zhao J. · American Journal of Translational Research. 2016;8(10):4472–4477.

PreclinicalOther formsPublished 2016Source checked
Study record, not medical adviceThis record reports what the source states. It is not medical advice and does not establish that molecular hydrogen is effective, safe or appropriate for any person.
Quick summary

Study at a glance

Evidence type

Preclinical

Population or model

Male DBA/1J mice with collagen-induced arthritis and a cultured human rheumatoid-arthritis fibroblast-like synovial cell line.

Intervention and dose

Beginning seven days after primary immunization, mice received hydrogen-saturated saline at 10 mL/kg/day for 45 days. Cultured cells received 0.6 mmol/L H₂-enriched medium together with 0.8 mmol/L hydrogen peroxide for 24 hours, with additional measurements through 72 hours. · Hydrogen was dissolved for two hours at 0.4 MPa and the fresh solution was reported above 0.6 mmol/L; cell medium was used at 0.6 mmol/L.

Duration

Forty-five days of mouse treatment starting seven days after primary immunization; cell assays covered 24–72 hours.

Reported result

The article reports lower arthritis incidence and scores and less histological damage in hydrogen-treated mice, with changes in oxidative-stress and signaling measures in cultured cells. Exact numerical animal values and uncertainty estimates are sparse in the text and figures.

Main limitation

Small mouse groups, mixed animal and cell experiments, sparse numerical reporting and no human treatment arm. The article calls the mouse intervention 'oral hydrogen' in one passage but describes daily intraperitoneal hydrogen-saturated saline in the preparation/administration paragraph; Hydrogenology preserves this unresolved route inconsistency rather than choosing silently. Chinese PLA, National Natural Science Foundation of China and Jiangsu clinical-research grants funded the work; authors disclosed no conflict of interest.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Controlled collagen-induced-arthritis mouse experiment with complementary human rheumatoid-synovial-cell assays

Research topic

Musculoskeletal and pain research

Administration form

Other forms

Information not yet classified

Some editorial classification fields are still pending. The source-reported outcomes and result are shown below; Hydrogenology does not infer a positive or negative signal from prose automatically.

Reported in the source

Methods

Population or model

Male DBA/1J mice with collagen-induced arthritis and a cultured human rheumatoid-arthritis fibroblast-like synovial cell line.

Sample

Mouse groups were normal control n=10, collagen-induced arthritis plus saline n=10 and collagen-induced arthritis plus hydrogen n=10; the article does not report one consolidated sample count for the repeated cell assays.

Duration

Forty-five days of mouse treatment starting seven days after primary immunization; cell assays covered 24–72 hours.

Intervention

Beginning seven days after primary immunization, mice received hydrogen-saturated saline at 10 mL/kg/day for 45 days. Cultured cells received 0.6 mmol/L H₂-enriched medium together with 0.8 mmol/L hydrogen peroxide for 24 hours, with additional measurements through 72 hours.

Hydrogen form

H₂ dissolved in saline or culture medium — H₂ only, not Brown's gas and not inhalation.

Dose or H₂ specification

Hydrogen was dissolved for two hours at 0.4 MPa and the fresh solution was reported above 0.6 mmol/L; cell medium was used at 0.6 mmol/L.

Comparator

Saline-treated arthritic mice, non-arthritic controls and matched cell-culture controls.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Arthritis incidence and score, joint histology, synovial-cell proliferation, superoxide dismutase, glutathione, 8-OHdG, MAPK, NF-κB and TGF-β1 signaling.

Reported result

The article reports lower arthritis incidence and scores and less histological damage in hydrogen-treated mice, with changes in oxidative-stress and signaling measures in cultured cells. Exact numerical animal values and uncertainty estimates are sparse in the text and figures.

Extraction completeness

The complete open-access article, mouse allocation, preparation and concentration, animal and cell protocols, reported results, funding and conflict statement were checked.

A reported association, difference or mechanism is not automatically a clinical benefit.

Interpretation limits

Limitations and applicability

Main methodological cautions

Small mouse groups, mixed animal and cell experiments, sparse numerical reporting and no human treatment arm. The article calls the mouse intervention 'oral hydrogen' in one passage but describes daily intraperitoneal hydrogen-saturated saline in the preparation/administration paragraph; Hydrogenology preserves this unresolved route inconsistency rather than choosing silently. Chinese PLA, National Natural Science Foundation of China and Jiangsu clinical-research grants funded the work; authors disclosed no conflict of interest.

Applies directly to

Collagen-induced arthritis in mice and cultured synovial cells; it does not establish efficacy or dosing in people with rheumatoid arthritis.

No single-study GRADE certainty rating is assigned. Read how records and evidence assessments are prepared.

Sources and status

Sources and record status

Identifiers

PMID: 27830032

Publisher access

Open-access PubMed Central article.

Extraction basis

Complete PubMed Central article and PubMed metadata; full-text extraction checked 9 August 2026.

Last reviewed

10 August 2026

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