Hydrogenology
Hydrogenology editorial study record

Estimation of the hydrogen concentration in rat tissue using an airtight tube following the administration of hydrogen via various routes

Liu C, Kurokawa R, Fujino M, Hirano S, Sato B, Li XK. · 2014.

PreclinicalInhaled H₂Published 2014
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 rat pharmacokinetic-distribution study

Research topic

Other molecular hydrogen research

Administration classification

Inhaled H₂

Study result signal

Route- and concentration-dependent distribution signal.

Outcome type

Animal pharmacokinetic and tissue-distribution outcomes.

Reported in the source

Methods at a glance

Population or model

Rats receiving molecular hydrogen by several administration routes.

Sample

Route-specific animal and tissue counts were checked; no single consolidated total is reported.

Duration

Acute administration with serial tissue measurements.

Intervention

Hydrogen inhalation and other article-specified routes, with tissue hydrogen measured in airtight sampling tubes.

Hydrogen form

Inhaled H₂ and H₂ delivered by other tested routes.

H₂ specification

The article compared multiple gas concentrations and administration conditions.

H₂ flow

Article-specific chamber delivery; no single flow applies to every arm.

O₂ delivered with H₂

Carrier conditions varied by administration arm.

Comparator

Baseline and route or concentration comparisons.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Hydrogen concentrations in blood and multiple tissues.

Reported result

Blood and tissue hydrogen rose after administration, with magnitude and time course differing by route and inhaled concentration.

Results-extraction completeness

The full article was checked for methods, intervention details, outcomes, positive and null findings, funding and conflicts. This record does not imply medical efficacy.

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

Pharmacokinetic animal study; tissue concentrations are not evidence of therapeutic benefit.

Applies directly to

The reported rat administration and sampling methods only.

Preliminary appraisal framework

SYRCLE animal-study tool — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Controlled exposure comparisons were used, but allocation, blinding and assay-selection details were incompletely reported.

Appraisal domains

Sequence generation checked where reported · Allocation concealment generally unclear · Personnel blinding generally unclear · Outcome-assessor blinding generally unclear · No prospectively registered analysis plan identified

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: 24975958 · DOI: 10.1038/srep05485

Publisher access

A free full article is available through PubMed Central.

Extraction basis

Official PubMed Central full article and PubMed bibliographic record; source identity, methods, intervention, results, funding and conflicts checked 10 August 2026.

Record revision

2026-08-10