Hydrogenology
Hydrogenology editorial study record

The reason for the amelioration of N-methyl-N-nitrosourea-induced retinitis pigmentosa in rats by hydrogen-rich saline

Yan WM, Chen T, Wang XC, Qi LS, Zhao GH, Yang GQ, Ma YF, Tao Y, Zhang L, Zhang ZM. · International Journal of Ophthalmology. 2017;10(10):1495-1503.

PreclinicalOther formsPublished 2017
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Preclinical

Reported design

Randomized three-group controlled rat study

Research topic

Eye health

Administration classification

Other forms

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Seventy-two rats allocated to normal, MNU retinal-degeneration model, and MNU plus H₂-rich saline groups.

Sample

72 rats, n=24 per group. Functional/histological time-point analyses used n=6 per group and molecular assays commonly used n=3 per group.

Duration

Daily pretreatment for 14 days plus continued dosing until day-1 or day-3 assessment after MNU.

Intervention

H₂-rich saline 10 mL/kg intraperitoneally once daily from 14 days before MNU administration until sacrifice one or three days afterward.

Hydrogen form

H₂ dissolved in saline — H₂ only, not Brown's gas.

H₂ specification

Purified hydrogen was dissolved in saline for six hours at 0.4 MPa; solution was stored at 4°C, made weekly and confirmed by gas chromatography to remain above 0.6 mmol/L.

H₂ flow

Not applicable — intraperitoneal saline, not gas inhalation.

O₂ delivered with H₂

No O₂ was co-delivered as part of the intervention.

Comparator

Normal rats and MNU model rats receiving equal-volume normal saline.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Outer nuclear-layer thickness, electroretinographic b-wave, retinal microglia/Iba1 and Sirt1 mRNA and protein.

Reported result

H₂-rich saline preserved retinal structure and b-wave amplitude and was associated with higher Sirt1 by day 3. Microglial/Iba1 measures were higher than the untreated model on day 1 but lower by day 3; Sirt1 mRNA was higher at both points but statistically significant at day 3, and Sirt1 protein differed significantly at day 3. The short study did not test inherited retinitis pigmentosa or durable vision.

Results-extraction completeness

The complete free PMC article was checked for allocation, H₂ preparation and concentration, dose, prophylactic schedule, structural, functional and molecular results including time-dependent/null findings, funding and conflict declarations.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Chemical retinal-injury model, prophylactic H₂ exposure beginning 14 days before injury, short one-to-three-day follow-up, small molecular assay samples and no human participants. Chinese national/provincial grants funded the work; every author declared no conflict of interest.

Applies directly to

Acute MNU-induced photoreceptor degeneration in rats; it does not establish treatment for inherited retinitis pigmentosa in people.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 29062766 · DOI: 10.18240/ijo.2017.10.03

Publisher access

Free full article in PubMed Central.

Extraction basis

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

Record revision

2026-08-10