Hydrogenology
Hydrogenology editorial study record

Oral Administration of Si-Based Agent Attenuates Oxidative Stress and Ischemia-Reperfusion Injury in a Rat Model: A Novel Hydrogen Administration Method.

Kawamura M, Imamura R, Kobayashi Y, Taniguchi A, Nakazawa S, Kato T, Namba-Hamano T, Abe T, Uemura M, Kobayashi H, Nonomura N. · 2020.

PreclinicalOther formsPublished 2020
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 kidney ischemia-reperfusion study

Research topic

Kidney and urinary health

Administration classification

Other forms

Study result signal

Positive preclinical signal for the nano-silicon condition.

Outcome type

Animal renal-function, tissue and molecular outcomes.

Reported in the source

Methods at a glance

Population or model

Rats with renal ischemia-reperfusion injury.

Sample

Four experimental groups; animal and assay counts were checked in the full article.

Duration

Outcomes through 72 hours after ischemia-reperfusion.

Intervention

Oral nano-silicon particles that generate molecular hydrogen after reacting with water.

Hydrogen form

Oral H₂-generating silicon agent.

H₂ specification

Nano-silicon and larger-particle silicon arms were compared; systemic H₂ dose was not directly measured.

H₂ flow

Not applicable.

O₂ delivered with H₂

No oxygen was co-delivered.

Comparator

Sham, untreated injury, nano-silicon and large-silicon groups.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Creatinine, urine protein, oxidative markers, inflammation, apoptosis and transcriptomics.

Reported result

Nano-silicon was associated with lower renal-injury and oxidative measures and altered inflammatory or apoptotic pathways versus untreated injury.

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

The intervention is a hydrogen-generating silicon product; particle-size and material effects cannot be assigned solely to H₂.

Applies directly to

The reported rat kidney-injury and silicon-agent protocol only.

Preliminary appraisal framework

SYRCLE animal-study tool — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Multiple controlled groups were present, but concealment, blinded assessment and material-specific confounding were unclear.

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: 32266279 · DOI: 10.3389/fmed.2020.00095

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