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Source-linked study record

Molecular hydrogen reduces LPS-induced neuroinflammation and promotes recovery from sickness behaviour in mice

Spulber S et al. · PLoS One. 2012;7(7):e42078.

PreclinicalH₂-rich waterPublished 2012Source checked
Study record, not medical adviceThis record reports what the source states. It is not medical advice and does not establish that molecular hydrogen is effective, safe or appropriate for any person.
Quick summary

Study at a glance

Evidence type

Preclinical

Population or model

Mice receiving lipopolysaccharide to induce systemic inflammation and sickness behavior

Intervention and dose

Hydrogen-enriched electrochemically reduced drinking water ad libitum, started 7 days before LPS and continued afterward · Drinking water contained 510.8 ± 21.9 ppb dissolved H₂; H₂-rich cell medium contained 78.5 ± 20.1 ppb.

Duration

Seven-day preadministration followed by continued intake during behavioral and tissue follow-up

Reported result

The article reports less sickness behavior and faster behavioral recovery. Baseline TNF-α decreased and IL-10 increased; the neuroinflammatory response was described as larger in amplitude but shorter in duration.

Main limitation

Mouse endotoxin model with multiple behavioral and molecular cohorts. An employee of Nihon-Trim was an author and the company funded the study.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Controlled mouse endotoxin experiment with behavioral, inflammatory and gene-expression cohorts

Research topic

Immune and inflammatory conditions

Administration form

H₂-rich water

Information not yet classified

Some editorial classification fields are still pending. The source-reported outcomes and result are shown below; Hydrogenology does not infer a positive or negative signal from prose automatically.

Reported in the source

Methods

Population or model

Mice receiving lipopolysaccharide to induce systemic inflammation and sickness behavior

Sample

Behavioral cohorts included sham/control n=15, sham/H₂ n=15, LPS/control n=13 and LPS/H₂ n=14; additional home-cage and tissue cohorts were smaller

Duration

Seven-day preadministration followed by continued intake during behavioral and tissue follow-up

Intervention

Hydrogen-enriched electrochemically reduced drinking water ad libitum, started 7 days before LPS and continued afterward

Hydrogen form

H₂ dissolved in drinking water — H₂ only, not Brown’s gas and not inhalation.

Dose or H₂ specification

Drinking water contained 510.8 ± 21.9 ppb dissolved H₂; H₂-rich cell medium contained 78.5 ± 20.1 ppb.

Comparator

Ordinary drinking water in sham-treated and LPS-treated mice

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Body weight, spontaneous and novel-environment behavior, brain and peripheral cytokines and inflammatory gene expression

Reported result

The article reports less sickness behavior and faster behavioral recovery. Baseline TNF-α decreased and IL-10 increased; the neuroinflammatory response was described as larger in amplitude but shorter in duration.

Extraction completeness

The complete open-access article was checked for water characterization, allocation, behavioral and molecular outcomes, funding and conflicts.

A reported association, difference or mechanism is not automatically a clinical benefit.

Interpretation limits

Limitations and applicability

Main methodological cautions

Mouse endotoxin model with multiple behavioral and molecular cohorts. An employee of Nihon-Trim was an author and the company funded the study.

Applies directly to

LPS-induced sickness and neuroinflammation in mice, not a clinical neurological or infectious disease.

No single-study GRADE certainty rating is assigned. Read how records and evidence assessments are prepared.

Sources and status

Sources and record status

Identifiers

PMID: 22860058 · DOI: 10.1371/journal.pone.0042078

Publisher access

Open-access full text is available through PMC and PLOS.

Extraction basis

Open-access PMC/PLOS full text and PubMed record.

Last reviewed

10 August 2026

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