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The Evaluation and Quantitation of Dihydrogen Metabolism Using Deuterium Isotope in Rats
R. Hyspler, A. Ticha, H. Schierbeek, A. Galkin, Z. Zadak,
Language English Country United States
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT13536
MZ0
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Digital library NLK
Full text - Article
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- MeSH
- Antioxidants metabolism pharmacology MeSH
- Ascitic Fluid metabolism MeSH
- Deuterium pharmacokinetics MeSH
- Endotoxins pharmacology MeSH
- Hyperoxia metabolism MeSH
- Hypoxia metabolism MeSH
- Rats MeSH
- Carbon Monoxide analysis MeSH
- Oxidative Stress drug effects MeSH
- Rats, Wistar MeSH
- Drug Evaluation, Preclinical MeSH
- Electron Transport Complex I drug effects metabolism MeSH
- Respiratory Burst drug effects MeSH
- Free Radical Scavengers metabolism pharmacology MeSH
- Cattle MeSH
- Mitochondria, Heart metabolism MeSH
- Superoxides metabolism MeSH
- Body Water metabolism MeSH
- Tissue Distribution MeSH
- Hydrogen metabolism pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Cattle MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
PURPOSE: Despite the significant interest in molecular hydrogen as an antioxidant in the last eight years, its quantitative metabolic parameters in vivo are still lacking, as is an appropriate method for determination of hydrogen effectivity in the mammalian organism under various conditions. BASIC PROCEDURES: Intraperitoneally-applied deuterium gas was used as a metabolic tracer and deuterium enrichment was determined in the body water pool. Also, in vitro experiments were performed using bovine heart submitochondrial particles to evaluate superoxide formation in Complex I of the respiratory chain. MAIN FINDINGS: A significant oxidation of about 10% of the applied dose was found under physiological conditions in rats, proving its antioxidant properties. Hypoxia or endotoxin application did not exert any effect, whilst pure oxygen inhalation reduced deuterium oxidation. During in vitro experiments, a significant reduction of superoxide formation by Complex I of the respiratory chain was found under the influence of hydrogen. The possible molecular mechanisms of the beneficial effects of hydrogen are discussed, with an emphasis on the role of iron sulphur clusters in reactive oxygen species generation and on iron species-dihydrogen interaction. PRINCIPAL CONCLUSIONS: According to our findings, hydrogen may be an efficient, non-toxic, highly bioavailable and low-cost antioxidant supplement for patients with pathological conditions involving ROS-induced oxidative stress.
Division of Mother and Child University of Amsterdam Amsterdam Netherlands
School of Biological Sciences Queen's University Belfast United Kingdom
References provided by Crossref.org
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