Hydrogenology
Hydrogenology editorial study record

Experimental verification of protective effect of hydrogen-rich water against cisplatin-induced nephrotoxicity in rats using dynamic contrast-enhanced CT

Kitamura A, Kobayashi S, Matsushita T, Fujinawa H, Murase K. · British Journal of Radiology. 2010;83(990):509.

PreclinicalH₂-rich waterPublished 2010
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

Three-group controlled rat study with repeated dynamic contrast-enhanced CT

Research topic

Kidney and urinary health

Administration classification

H₂-rich water

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

Thirty eight-week-old male Sprague-Dawley rats in a cisplatin-nephrotoxicity model.

Sample

30 rats: untreated control n=6, cisplatin with standard water n=12, and cisplatin with H₂-rich water n=12.

Duration

H₂ water from seven days before cisplatin through the final day-7 assessment; CT on days 0, 2, 4 and 7.

Intervention

Ad-libitum H₂-rich water beginning seven days before intraperitoneal cisplatin 3.6 mg/kg and continuing through day 7 after injection.

Hydrogen form

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

H₂ specification

Dissolved H₂ concentration was 1.2 ± 0.1 mg/L in sealed 200 mL aluminium pouches. Daily water intake and ingested H₂ dose per kg were not reported.

H₂ flow

Not applicable — drinking water, not gas inhalation.

O₂ delivered with H₂

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

Comparator

Healthy rats with standard water and cisplatin-treated rats with standard water.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Renal contrast clearance per tissue volume and for the whole kidney, renal volume, serum creatinine, body weight and renal histopathology.

Reported result

Normalized renal-clearance measures were higher with H₂ water than with cisplatin plus standard water on days 2, 4 and 7; day-7 creatinine and tubular damage were lower. The treatment and healthy-control groups did not differ significantly for normalized whole-kidney clearance on days 2 and 7 or for serum creatinine. Whole-kidney clearance still fell significantly from baseline on day 4 in the H₂ group.

Results-extraction completeness

The complete free PMC article was checked for all groups, water concentration and timing, functional and histological outcomes, null comparisons, safety comments, commercial material provision and available disclosures.

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

Small animal study, unequal group sizes, preventive exposure starting before cisplatin, ad-libitum intake not quantified, short seven-day follow-up, repeated iodinated-contrast imaging and no assessment of cisplatin antitumour efficacy in this experiment. I'rom Pharmaceutical provided the H₂ water and one author was affiliated with that company; no explicit funding or conflict declaration was identified, so absence is not inferred.

Applies directly to

Experimental cisplatin nephrotoxicity in rats; it does not establish kidney protection in patients receiving chemotherapy.

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: 20505032 · DOI: 10.1259/bjr/25604811

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