Hydrogenology
Hydrogenology editorial study record

Molecular hydrogen suppresses free-radical-induced cell death by mitigating fatty acid peroxidation and mitochondrial dysfunction

Iuchi K, Nishimaki K, Kamimura N, Ohta S. · Can J Physiol Pharmacol. 2019;97(10):999–1005.

PreclinicalOther formsPublished 2019
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

Controlled cell-culture study

Research topic

Cardiovascular and circulatory health

Administration classification

Other forms

Study result signal

Positive cell-culture signal.

Outcome type

Cell viability and mechanistic laboratory outcomes.

Reported in the source

Methods at a glance

Population or model

THP-1 cells, with confirmatory experiments in human aortic endothelial cells.

Sample

Three to four independent replicate experiments per reported assay.

Duration

4.5 to 18 hours depending on assay.

Intervention

Cell exposure to 75% or 10% H₂-containing gas.

Hydrogen form

H₂ gas applied to cell-culture systems.

H₂ specification

75% or 10% H₂, depending on the experiment.

H₂ flow

Cell-culture chamber exposure.

O₂ delivered with H₂

Control gas conditions were matched as reported.

Comparator

0% H₂ gas and oxidative-injury controls.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Cell death, LDH release, lipid peroxidation and mitochondrial function.

Reported result

H₂ exposure reduced several free-radical-related cell-injury measures in the tested systems.

Results-extraction completeness

The full article methods, intervention, outcomes, positive and null findings, funding and conflict statements were checked.

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

Cell-only evidence with high gas concentrations; it does not establish a clinical effect.

Applies directly to

The tested cell systems and exposure conditions only.

Preliminary appraisal framework

In-vitro study appraisal — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Small replicate counts, assay-level multiplicity and generally unreported blinding.

Appraisal domains

Independent replicate reporting checked · Exposure and comparator checked · Assay blinding generally unreported · Multiplicity and selective reporting remain possible · External validity is limited to the tested cells

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: 31295412 · DOI: 10.1139/cjpp-2018-0741

Publisher access

A free publisher or repository full article was checked.

Extraction basis

Publisher or repository full article and bibliographic record; checked 10 August 2026.

Record revision

2026-08-10