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Hydrogen exerts neuroprotective effects by inhibiting oxidative stress in experimental diabetic peripheral neuropathy rats

Han XC, Ye ZH, Hu HJ, Sun Q, Fan DF. · Medical Gas Research. 2023;13(2):72–77.

PreclinicalOther formsPublished 2023Source 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

Adult male Sprague-Dawley rats with diabetes induced by a single intraperitoneal 65 mg/kg streptozotocin injection.

Intervention and dose

Beginning three days after diabetes induction, rats received hydrogen-rich saline 10 mL/kg by intraperitoneal injection once daily; no insulin or antidiabetic drugs were given. · Hydrogen was dissolved in saline for 3 hours at 0.4 MPa and the solution was prepared one day before use; gas chromatography confirmed a target concentration of 0.6 mmol/L.

Duration

Daily treatment for eight weeks.

Reported result

Hydrogen-rich saline partially restored motor nerve-conduction velocity and myelinated-nerve density and area and reduced the reported oxidative-stress measures while increasing SOD and Nrf2-pathway proteins versus untreated diabetic rats. Body-mass gain remained non-significantly different from untreated diabetes at weeks 4 and 8 (p>0.05).

Main limitation

Preclinical model with only eight rats per group, one sex, many biochemical outcomes and no behavioral pain testing or long-term post-treatment follow-up. The abstract incorrectly contrasts 'hydrogen inhalation' with hydrogen-rich saline, while the Methods describe only daily intraperitoneal hydrogen-rich saline; the structured record follows the Methods and flags the discrepancy. The Innovation Cultivation Foundation of Navy General Hospital funded the work; authors declared no conflicts of interest.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Randomized three-group streptozotocin-induced diabetes experiment

Research topic

Metabolic and lipid 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

Adult male Sprague-Dawley rats with diabetes induced by a single intraperitoneal 65 mg/kg streptozotocin injection.

Sample

24 rats randomized to healthy control, untreated diabetes and diabetes plus hydrogen-rich saline, n=8 per group.

Duration

Daily treatment for eight weeks.

Intervention

Beginning three days after diabetes induction, rats received hydrogen-rich saline 10 mL/kg by intraperitoneal injection once daily; no insulin or antidiabetic drugs were given.

Hydrogen form

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

Dose or H₂ specification

Hydrogen was dissolved in saline for 3 hours at 0.4 MPa and the solution was prepared one day before use; gas chromatography confirmed a target concentration of 0.6 mmol/L.

Comparator

Diabetic rats receiving the same 10 mL/kg volume of ordinary physiological saline and non-diabetic controls receiving vehicle.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Body-mass gain, blood glucose, motor nerve-conduction velocity, sciatic-nerve myelin morphology and density, malondialdehyde, reactive oxygen species, 8-hydroxy-2-deoxyguanosine, superoxide dismutase and Nrf2, heme oxygenase-1 and catalase protein expression.

Reported result

Hydrogen-rich saline partially restored motor nerve-conduction velocity and myelinated-nerve density and area and reduced the reported oxidative-stress measures while increasing SOD and Nrf2-pathway proteins versus untreated diabetic rats. Body-mass gain remained non-significantly different from untreated diabetes at weeks 4 and 8 (p>0.05).

Extraction completeness

The complete open-access article, allocation, saline preparation, concentration and dose, positive and null results, funding and conflict statement were checked.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Preclinical model with only eight rats per group, one sex, many biochemical outcomes and no behavioral pain testing or long-term post-treatment follow-up. The abstract incorrectly contrasts 'hydrogen inhalation' with hydrogen-rich saline, while the Methods describe only daily intraperitoneal hydrogen-rich saline; the structured record follows the Methods and flags the discrepancy. The Innovation Cultivation Foundation of Navy General Hospital funded the work; authors declared no conflicts of interest.

Applies directly to

Streptozotocin-induced diabetic peripheral-nerve injury in rats; it does not establish treatment efficacy, dosing or safety in people with diabetic neuropathy.

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: 36204786 · DOI: 10.4103/2045-9912.345171

Publisher access

Open-access Medical Gas Research article and PubMed Central copy.

Extraction basis

Complete PubMed Central/Medical Gas Research article and PubMed metadata; full-text extraction checked 9 August 2026.

Last reviewed

10 August 2026

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