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Hydrogen-rich saline promotes recovery of renal function after ischemia-reperfusion injury in rats via anti-apoptosis and anti-inflammation

Li Y et al. · Front Pharmacol. 2016;7:106.

PreclinicalOther formsPublished 2016Source 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

Rats after right nephrectomy and 45-minute left renal-pedicle occlusion

Intervention and dose

0.6 mmol/L hydrogen-rich saline, 1 mL/kg intraperitoneally immediately after reperfusion and every 4 hours · 0.6 mmol/L dissolved H₂; saline was saturated for 6 hours at 0.4 MPa and verified by gas chromatography.

Duration

Short 24-hour treatment or continuous treatment through 108 hours

Reported result

The article reports less histologic injury and faster BUN and creatinine recovery with H₂ saline. Renal-function measures worsened again after the short treatment was stopped compared with continuous treatment.

Main limitation

Preclinical renal-ischemia model with nephrectomy, frequent injections and multiple time points. The article contains internally confusing wording about Bcl-2/Bax direction that requires independent verification.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Controlled rat unilateral-renal-ischemia experiment comparing short and continuous H₂-saline schedules

Research topic

Kidney and urinary 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

Rats after right nephrectomy and 45-minute left renal-pedicle occlusion

Sample

120 rats: sham n=30, ischemia/reperfusion n=30, continuous H₂-saline n=30 and 24-hour H₂-saline n=30

Duration

Short 24-hour treatment or continuous treatment through 108 hours

Intervention

0.6 mmol/L hydrogen-rich saline, 1 mL/kg intraperitoneally immediately after reperfusion and every 4 hours

Hydrogen form

H₂ dissolved in saline — H₂ only, not Brown’s gas and not inhalation.

Dose or H₂ specification

0.6 mmol/L dissolved H₂; saline was saturated for 6 hours at 0.4 MPa and verified by gas chromatography.

Comparator

Ischemia-reperfusion rats receiving ordinary saline and sham-operated controls

Reported, not endorsed

Outcomes and reported result

Outcomes measured

BUN, creatinine, histology, apoptosis and Bcl-2, Bax, caspases, IL-6 and TNF-α

Reported result

The article reports less histologic injury and faster BUN and creatinine recovery with H₂ saline. Renal-function measures worsened again after the short treatment was stopped compared with continuous treatment.

Extraction completeness

The complete open-access article was checked for preparation, concentration, allocation, dose, schedules and principal positive and null results.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Preclinical renal-ischemia model with nephrectomy, frequent injections and multiple time points. The article contains internally confusing wording about Bcl-2/Bax direction that requires independent verification.

Applies directly to

Renal ischemia-reperfusion after contralateral nephrectomy in rats.

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: 27148060 · DOI: 10.3389/fphar.2016.00106

Publisher access

Open-access full text is available through PMC and Frontiers.

Extraction basis

Open-access PMC/Frontiers full text and PubMed record.

Last reviewed

10 August 2026

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