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Molecular hydrogen regulates the expression of miR-9, miR-21 and miR-199 in LPS-activated retinal microglia cells

Liu GD, Zhang H, Wang L, Han Q, Zhou SF, Liu P. · International Journal of Ophthalmology. 2013;6(3):280-285.

PreclinicalOther formsPublished 2013Source 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

Retinal microglia cell line exposed to LPS in culture; no animals or patients were studied.

Intervention and dose

After 36 hours with or without LPS, cells received hydrogen-saturated DMEM/F12 for 24 hours. · H₂ medium was prepared under 0.5 MPa and mixed with O₂- and CO₂-saturated media at 75:20:5 by volume. The article reports an initial calibrated H₂ concentration of 1.0×10⁻⁶ and not less than 0.5×10⁻⁶ after 24 hours, but does not state the unit for those two values; O₂-saturated medium is reported as 42 mg/L.

Duration

Thirty-six-hour LPS exposure followed by 24-hour H₂-medium treatment.

Reported result

After LPS, H₂ medium was associated with higher cell survival, lower miR-9/miR-21, higher miR-199, lower Myd88/IKK-β and higher PDCD4. NF-κB expression did not differ significantly between LPS and LPS plus H₂, and the control-plus-H₂ condition showed no significant survival change.

Main limitation

In-vitro single-cell-line model, no organism-level outcome, unclear biological-replicate total, missing units for the stated H₂ concentration values and multiple mechanistic comparisons. No funding or conflict statement was identified in the article, so absence is not inferred.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Four-condition in-vitro retinal-microglia experiment

Research topic

Eye health

Administration form

Other forms

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

Retinal microglia cell line exposed to LPS in culture; no animals or patients were studied.

Sample

Four conditions: control, 100 ng/mL LPS, control plus H₂ medium and LPS plus H₂ medium. qRT-PCR was performed in quadruplicate; a single biological-replicate total was not reported.

Duration

Thirty-six-hour LPS exposure followed by 24-hour H₂-medium treatment.

Intervention

After 36 hours with or without LPS, cells received hydrogen-saturated DMEM/F12 for 24 hours.

Hydrogen form

H₂ dissolved in cell-culture medium. Separate H₂-, O₂- and CO₂-saturated media were mixed; this was not inhaled Brown's gas.

Dose or H₂ specification

H₂ medium was prepared under 0.5 MPa and mixed with O₂- and CO₂-saturated media at 75:20:5 by volume. The article reports an initial calibrated H₂ concentration of 1.0×10⁻⁶ and not less than 0.5×10⁻⁶ after 24 hours, but does not state the unit for those two values; O₂-saturated medium is reported as 42 mg/L.

Comparator

Control and LPS-exposed cells in ordinary medium, plus control cells in H₂-saturated medium.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Cell survival, miR-9, miR-21, miR-199, Myd88, IKK-β, PDCD4 and NF-κB expression.

Reported result

After LPS, H₂ medium was associated with higher cell survival, lower miR-9/miR-21, higher miR-199, lower Myd88/IKK-β and higher PDCD4. NF-κB expression did not differ significantly between LPS and LPS plus H₂, and the control-plus-H₂ condition showed no significant survival change.

Extraction completeness

The complete free PMC article was checked for all four conditions, preparation method/composition, ambiguous concentration units, assay replication, positive and null findings, funding and available disclosures.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

In-vitro single-cell-line model, no organism-level outcome, unclear biological-replicate total, missing units for the stated H₂ concentration values and multiple mechanistic comparisons. No funding or conflict statement was identified in the article, so absence is not inferred.

Applies directly to

LPS-activated cultured retinal microglia; it does not establish treatment of retinal disease in humans.

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: 23826519 · DOI: 10.3980/j.issn.2222-3959.2013.03.05

Publisher access

Free full article in PubMed Central.

Extraction basis

Complete PMC article and PubMed metadata; full-text extraction checked 9 August 2026.

Last reviewed

10 August 2026

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