Hydrogen Research Study
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Preclinical animal evidenceAnimal studyOther or not reported

Gender-based differences in neuroprotective effects of hydrogen gas against intracerebral hemorrhage-induced depression.

An P, Zhao XC, Liu MJ, You YQ, Li JY · Neurochemistry international · 2022

Research-use notice

Independent study record

Each H2HUBB study page organizes source-linked research details for educational use. Interpretation should remain proportional to the study design, population, controls, and limitations.

H2HUBB Research Library branded molecular hydrogen research image
Primary topic Mental Health and Behavioral Conditions
Evidence type Preclinical animal evidence
Publication type Animal study
Hydrogen method Other or not reported
molecular hydrogen mental health study 2022 research summary

The publication “Gender-based differences in neuroprotective effects of hydrogen gas against intracerebral hemorrhage-induced depression.” is organized in H2HUBB under the research focus molecular hydrogen mental health study 2022. The publication is cited as An P, Zhao XC, Liu MJ, You YQ, Li JY, Neurochemistry international, 2022. This uncontrolled human study examined Gender-based differences in neuroprotective effects of hydrogen gas against intracerebral hemorrhage-induced depression. The abstract describes Human participants; reported duration 3 days. The abstract reports: Estrogen was responsible for increased H sensitivity in male mice with ICH. The underlying mechanism may be associated with the suppression of NF-κB signaling…. This is an automated editorial draft based on the abstract and requires source review before publication.

Molecular hydrogen mental health study 2022 overview

Post-stroke depression (PSD) severely affects recovery in patients with intracerebral hemorrhage (ICH). Although hydrogen gas (H) exerts excellent neuroprotective effects in patients with ICH,… Animal research can identify biological effects and support future investigation, but it cannot by itself establish safety or effectiveness in humans.

Study design and hydrogen intervention

Publication type: Animal study. Evidence type: Preclinical animal evidence. Research model or population: Mouse intracerebral-hemorrhage depression model. Blinding: Unknown. Control status: Unknown.

Delivery method: Other or not reported. Treatment duration: 3 days.

Reported findings and scientific interpretation

For this molecular hydrogen mental health study 2022, the study record reports the following: The abstract reports: Estrogen was responsible for increased H sensitivity in male mice with ICH. The underlying mechanism may be associated with the suppression of NF-κB signaling…

These findings should be interpreted as one piece of evidence rather than as a stand-alone medical conclusion. Results can be influenced by the research model, study design, treatment protocol, sample size, outcome selection, statistical methods, and whether the findings have been independently reproduced.

How this research record was prepared

H2HUBB organizes bibliographic details, study design information, intervention data, outcomes, limitations, and safety notes from the available scientific source. Automated classification supports database organization, but it does not replace critical reading of the complete paper. Source identifiers, evidence labels, and delivery-method fields are retained so readers can verify the record and compare it with related publications. A missing field means the information was unavailable or not reported in the structured source; it should not be treated as a negative finding.

Limitations, safety, and original source

Limitations: The intervention or follow-up period appears relatively short.

Safety: The abstract did not provide detailed safety or adverse-event information.

This H2HUBB page is an educational research record, not medical advice. Review the original scientific source for the complete methods and results. Continue exploring the H2HUBB Molecular Hydrogen Research Library to compare evidence types, delivery methods, and related topics.