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Source-linked study record

Protective effects of hydrogen-rich saline against renal ischemia-reperfusion injury by increased expression of heme oxygenase-1 in aged rats

Xu X, He X, Liu J, Qin J, Ye J, Fan M. · International Journal of Clinical and Experimental Pathology. 2019;12(4):1488-1496.

PreclinicalOther formsPublished 2019Source 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

Thirty 24-month-old male Sprague-Dawley rats undergoing sham surgery or 45-minute bilateral renal-pedicle occlusion.

Intervention and dose

H₂-rich saline 8 mL/kg intraperitoneally five minutes before reperfusion. · Hydrogen was dissolved for six hours at 0.4 MPa, gamma-sterilized and prepared weekly at 0.6 mM. The HTML text displays a storage temperature of 48°C, which appears implausible and may reflect a typesetting error; Hydrogenology does not silently replace it with 4°C.

Duration

Single injection five minutes before reperfusion; the main protocol states sacrifice 24 hours after ischemia.

Reported result

H₂-rich saline was associated with lower BUN/creatinine, oxidative-damage markers and histology score, higher SOD, and higher HO-1. BUN/creatinine did not differ from sham after H₂ treatment; HO-1 staining and mRNA did not differ significantly between untreated I/R and sham. One sentence reports p<0.05 while calling the HO-1 mRNA comparison non-significant, an internal inconsistency retained here.

Main limitation

Short preclinical study in aged male rats; one histology-method sentence refers to 12-week post-ischemic kidneys despite the main 24-hour protocol, the storage temperature is displayed implausibly as 48°C, and a non-significant comparison is paired with p<0.05. A Jiangsu medical foundation partly funded the study; authors disclosed no conflict.

Evidence and classification

What kind of evidence is this?

Evidence type

Preclinical

Reported design

Three-group controlled aged-rat ischemia-reperfusion experiment

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

Thirty 24-month-old male Sprague-Dawley rats undergoing sham surgery or 45-minute bilateral renal-pedicle occlusion.

Sample

30 aged rats, n=10 each in sham plus saline, renal I/R plus saline, and renal I/R plus H₂-rich saline groups.

Duration

Single injection five minutes before reperfusion; the main protocol states sacrifice 24 hours after ischemia.

Intervention

H₂-rich saline 8 mL/kg intraperitoneally five minutes before reperfusion.

Hydrogen form

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

Dose or H₂ specification

Hydrogen was dissolved for six hours at 0.4 MPa, gamma-sterilized and prepared weekly at 0.6 mM. The HTML text displays a storage temperature of 48°C, which appears implausible and may reflect a typesetting error; Hydrogenology does not silently replace it with 4°C.

Comparator

Age-matched sham plus saline and renal I/R plus normal saline.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

BUN, creatinine, renal MDA, 8-OHdG and SOD, histological injury, and HO-1 immunostaining/mRNA.

Reported result

H₂-rich saline was associated with lower BUN/creatinine, oxidative-damage markers and histology score, higher SOD, and higher HO-1. BUN/creatinine did not differ from sham after H₂ treatment; HO-1 staining and mRNA did not differ significantly between untreated I/R and sham. One sentence reports p<0.05 while calling the HO-1 mRNA comparison non-significant, an internal inconsistency retained here.

Extraction completeness

The complete free PMC article was checked for allocation, H₂ preparation/concentration, dose/timing, renal outcomes, null findings, internal method/result inconsistencies, funding and disclosure.

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

Interpretation limits

Limitations and applicability

Main methodological cautions

Short preclinical study in aged male rats; one histology-method sentence refers to 12-week post-ischemic kidneys despite the main 24-hour protocol, the storage temperature is displayed implausibly as 48°C, and a non-significant comparison is paired with p<0.05. A Jiangsu medical foundation partly funded the study; authors disclosed no conflict.

Applies directly to

Renal I/R in aged rats; it does not establish protection against human acute kidney injury.

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: 31933966

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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