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Hydrogen-Rich Water as a Novel Therapeutic Strategy for the Affective Disorders Linked with Chronic Neuropathic Pain in Mice

Martínez-Serrat M, Martínez-Martel I, Coral-Pérez S, Bai X, Batallé G, Pol O. · Antioxidants (Basel, Switzerland). 2022;11(9):1826.

PreclinicalH₂-rich waterPublished 2022Source 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, mouse, tissues, rabbit used to study other neurological conditions.

Intervention and dose

Full text reports H₂ dissolved in drinking water. Detected intervention quantities or schedules: 0.3 mM, 7 days, 4 days, 10 mL/kg. · H₂-related quantities reported in the intervention passages: 0.3 mM, 7 days, 4 days, 10 mL/kg. Values are not combined across different experimental arms.

Duration

7 days

Reported result

Article-reported result excerpt (24 words maximum): “The results showed: (i) the inhibitory effects of the repetitive treatment with HRW on the allodynia and hyperalgesia provoked by CCI; (ii) the anxiolytic…” This excerpt is not a complete result summary; consult the linked full text for all positive and null findings.

Main limitation

Preclinical evidence only; findings do not establish a treatment effect in people. Funding or grant information is reported in the full article. The article declares no conflicts of interest.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Controlled preclinical study

Research topic

Other neurological 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, mouse, tissues, rabbit used to study other neurological conditions.

Sample

Preclinical study; the article does not state one consolidated sample total, so no total is inferred.

Duration

7 days

Intervention

Full text reports H₂ dissolved in drinking water. Detected intervention quantities or schedules: 0.3 mM, 7 days, 4 days, 10 mL/kg.

Hydrogen form

H₂ dissolved in drinking water — H₂ only unless the full text explicitly reports oxygen co-delivery.

Dose or H₂ specification

H₂-related quantities reported in the intervention passages: 0.3 mM, 7 days, 4 days, 10 mL/kg. Values are not combined across different experimental arms.

Comparator

Control or comparison condition reported in the full article; see the linked methods for arm-specific details.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

survival or mortality, clinical symptoms or functional scores, inflammation and cytokines, oxidative-stress and antioxidant markers, apoptosis or cell injury, neurological or behavioral measures

Reported result

Article-reported result excerpt (24 words maximum): “The results showed: (i) the inhibitory effects of the repetitive treatment with HRW on the allodynia and hyperalgesia provoked by CCI; (ii) the anxiolytic…” This excerpt is not a complete result summary; consult the linked full text for all positive and null findings.

Extraction completeness

The complete machine-readable article was checked for source identity, methods, intervention quantities, results, tables, funding and conflict declarations. This public record is based on the full article.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Preclinical evidence only; findings do not establish a treatment effect in people. Funding or grant information is reported in the full article. The article declares no conflicts of interest.

Applies directly to

Applies to the reported animal, cell or tissue model, not directly to patients.

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: 36139900 · DOI: 10.3390/antiox11091826

Publisher access

A free full article is available through PubMed Central.

Extraction basis

Official Europe PMC JATS full article and PubMed/PMC identifiers; structured full-text extraction and validation completed 8 August 2026.

Last reviewed

10 August 2026

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