Hydrogenology
Hydrogenology editorial study record

Oral intake of hydrogen-rich water inhibits intimal hyperplasia in arterialized vein grafts in rats

Sun Q, Kawamura T, Masutani K, Peng X, Sun Q, Stolz DB, Pribis JP, Billiar TR, Sun X, Bermudez CA, Toyoda Y, Nakao A. · Cardiovascular Research. 2012;94(1):144-153.

PreclinicalH₂-rich waterPublished 2012
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 three-water rat vein-graft experiment with blood-H₂ kinetics and vascular-cell culture components

Research topic

Cardiovascular and circulatory 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

Lewis-rat abdominal aortic vein graft recipients, plus rat aortic smooth-muscle cells and human umbilical-vein endothelial cells in culture.

Sample

Tissue outcomes used n=5 per drinking-water group at one week and approximately n=5-6 at six weeks; culture experiments were repeated at least three times. A single total animal count is not reported.

Duration

One or six weeks of drinking-water exposure after grafting; in-vitro assays through 24-72 hours.

Intervention

Hydrogen-rich drinking water ad libitum immediately after vein grafting until tissue collection.

Hydrogen form

H₂ dissolved in drinking water — H₂ only, not Brown's gas.

H₂ specification

A magnesium stick generated 0.55-0.65 mmol/L H₂ water at pH 9.2-9.9, replaced every 24 hours. Separate culture medium contained 0.6 mmol/L H₂.

H₂ flow

Not applicable — drinking water/culture medium, not gas inhalation.

O₂ delivered with H₂

No O₂ was co-delivered as part of the intervention.

Comparator

Regular tap water and hydrogen water degassed for 48 hours, plus naive vein controls and ordinary culture medium.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Blood H₂ kinetics, intimal hyperplasia, macrophage/endothelial morphology, oxidative and inflammatory markers, MMP-2/9, smooth-muscle migration/proliferation and endothelial-cell injury.

Reported result

H₂ water increased blood H₂ transiently, reduced six-week intimal hyperplasia and multiple injury/inflammatory/migration measures, and preserved the endothelial surface. H₂ medium suppressed smooth-muscle migration but did not affect proliferation through 72 hours; H₂ intake did not affect ERK1/2 phosphorylation.

Results-extraction completeness

The complete free PMC article was checked for water preparation/concentration, comparators, timing, outcome-specific sample sizes, animal and cell outcomes, positive and null findings, funding and conflict declaration.

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

Preclinical surgical model, outcome-specific small groups, ad-libitum intake not quantified per animal, pH differed from ordinary water, multiple mechanistic endpoints and no graft-patency clinical endpoint. Public/foundation/NIH support was reported; authors declared no conflicts.

Applies directly to

Arterialized vein grafts in rats and vascular cells; it does not establish prevention of human bypass-graft failure.

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: 22287575 · DOI: 10.1093/cvr/cvs024

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