Hydrogenology
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Hydrogen ameliorates oxidative stress via PI3K-Akt signaling pathway in UVB-induced HaCaT cells

Zhang B, Zhao Z, Meng X, Chen H, Fu G, Xie K. · Int J Mol Med. 2018;41(6):3653–3661.

PreclinicalOther formsPublished 2018Source 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

HaCaT keratinocytes exposed to UVB radiation.

Intervention and dose

Hydrogen-rich culture medium after UVB exposure, with a PI3K inhibitor in mechanistic experiments. · 0.6 mmol/L dissolved H₂.

Duration

Up to 24 hours depending on assay.

Reported result

Several viability, oxidative, apoptotic and pathway measures favored hydrogen-rich medium after UVB exposure.

Main limitation

Cell-only evidence; pathway-inhibitor experiments are mechanistic and do not establish patient benefit.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Controlled cell-culture study

Research topic

Skin, wound and aging research

Administration form

Other forms

Study result signal

Positive cell-culture signal.

Outcome type

Cell viability and mechanistic pathway outcomes.

Reported in the source

Methods

Population or model

HaCaT keratinocytes exposed to UVB radiation.

Sample

Approximately five to six independent observations per assay as reported.

Duration

Up to 24 hours depending on assay.

Intervention

Hydrogen-rich culture medium after UVB exposure, with a PI3K inhibitor in mechanistic experiments.

Hydrogen form

H₂ dissolved in cell-culture medium.

Dose or H₂ specification

0.6 mmol/L dissolved H₂.

Comparator

UVB-exposed and non-exposed conventional medium, with pathway-inhibitor comparisons.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Cell viability, ROS, oxidative markers, apoptosis and PI3K/Akt/FoxO signaling.

Reported result

Several viability, oxidative, apoptotic and pathway measures favored hydrogen-rich medium after UVB exposure.

Extraction completeness

The full article methods, intervention, outcomes, positive and null findings, funding and conflict statements were checked.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Cell-only evidence; pathway-inhibitor experiments are mechanistic and do not establish patient benefit.

Applies directly to

The HaCaT cell model and tested exposure only.

Preliminary appraisal framework

In-vitro study appraisal — preliminary

Preliminary risk-of-bias status

Some concerns

Appraisal rationale

Assay comparators were present, but replicate-level randomization, blinding and multiplicity control were not established.

Appraisal domains

Independent replicate reporting checked · Exposure and comparator checked · Assay blinding generally unreported · Multiplicity and selective reporting remain possible · External validity is limited to the tested cells

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: 29532858 · DOI: 10.3892/ijmm.2018.3550

Publisher access

A free publisher or repository full article was checked.

Extraction basis

Publisher or repository full article and bibliographic record; checked 10 August 2026.

Last reviewed

10 August 2026

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