Hydrogenology
Hydrogenology editorial study record

The gastroprotective effect of hydrogen-rich coral calcium in a mouse model of peptic ulcer disease

Wu HT, Hsieh MT, Ou HY, Chao TH, Tsai LM. · Drug Design, Development and Therapy. 2025;19:9845–9851.

PreclinicalH₂-rich waterPublished 2025
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Preclinical

Reported design

Randomized four-group mouse HCl/ethanol gastric-injury study with ex-vivo and seven-day in-vivo experiments

Research topic

Gastrointestinal health

Administration classification

H₂-rich water

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Eight-week-old male C57BL/6 mice exposed to hydrochloric-acid/60% ethanol gastric injury.

Sample

Four groups of six mice were reported; selected Western blots used n=3/group. Whether the ex-vivo and in-vivo stages used distinct animal cohorts is not made explicit.

Duration

Thirty-minute pretreatment before acute ex-vivo injury or once-daily pretreatment/injury for seven days in vivo.

Intervention

Oral hydrogen-rich coral calcium (HRCC) before HCl/ethanol injury, compared with non-hydrogen porous coral calcium.

Hydrogen form

H₂ held/released by an oral coral-calcium product — not Brown's gas, not inhaled H₂ and not H₂-rich water.

H₂ specification

The actual study batch's H₂ content/release was not measured. The introduction cites up to 14.72 ppm in water for this technology generally, which is not treated as the administered dose. The methods list 105/210 mg/kg, while figure legends repeatedly list 210/420 mg/kg.

H₂ flow

Not applicable — oral solid/suspension; no gas flow was used.

O₂ delivered with H₂

No O₂ was co-administered.

Comparator

Porous coral calcium at a matched reported dose, with and without HCl/ethanol injury.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Macroscopic ulcer damage, gastric histology/immune infiltration, Tnfa/Ccl2/Il6 gene expression and catalase/GPx/SOD1 protein expression.

Reported result

HRCC groups showed less macroscopic/histologic gastric injury, lower inflammatory-gene expression and higher antioxidant-enzyme expression than injured coral-calcium controls, with reported dose gradients. Interpretation is limited by the unresolved two-fold dose discrepancy and absence of measured product H₂ exposure.

Results-extraction completeness

The complete free PMC article, methods, figures and disclosures were checked for animal groups, oral route, coral-calcium comparator, absent H₂ assay, methods/figure dose discrepancy, all main outcomes, funding and conflicts.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Chemical-injury mouse model, preventive rather than therapeutic timing, small samples, selected assays n=3, unmeasured H₂ exposure, complex coral-calcium product and conflicting doses between methods and figure legends. A hospital managed by a medical-care corporation funded the study; authors declared no conflicts.

Applies directly to

Preventive gastric-injury findings in mice; they do not establish ulcer treatment, product dose or safety in humans.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 41221497 · DOI: 10.2147/DDDT.S555188

Publisher access

Free full article in PubMed Central.

Extraction basis

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

Record revision

2026-08-10