Aminotriazole effects on lung and heart H2O2 detoxifying enzymes and TBA-RS at two pO2.

Abstract

In order to clarify the physiological role in vivo of H2O2-detoxifying enzymes at low and high levels of O2 tension we studied catalase (CAT), glutathione peroxidases (GP), and in vivo peroxidation (TBA-RS) in the lung and heart of Rana perezi frogs chronically treated with hyperoxia, aminotriazole (AT) -a CAT inhibitor-, or both. Hyperoxia did not change CAT, GP or TBA-RS. Aminotriazole caused an almost complete depletion of CAT, a 30% decrease of GP and a 132% (lung) to 200% (heart) increase of TBA-RS. Changes similar to these were found in the group treated with AT in hyperoxia. No mortality or changes in total or organ weight occurred in the experimental groups. Main conclusions are: (1) The maximal hyperoxia tolerance showed by frogs among vertebrates does not need antioxidant enzyme induction from lung or heart and is probably related to the presence of high constitutive levels of GP in relation to metabolic rate. (2) Even in normoxia the tissues present significant amounts of H2O2, and CAT is needed to avoid oxidative damage. GP does not compensate its absence. The implications of these results in relation to oxygen toxicity in man is discussed.

• Authors: M López-Torres, R Pérez-Campo, G Barja de Quiroga
• Journal: Pharmacology & toxicology (Pharmacol Toxicol) Vol. 66 Issue 1 Pg. 27-31 (Jan 1990) ISSN: 0901-9928 [Print] Denmark
• PMID: 2308904 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Thiobarbiturates
• Triazoles
• Hydrogen Peroxide
• Catalase
• Glutathione Peroxidase
• thiobarbituric acid
• Amitrole

Topics

• Amitrole (pharmacology)
• Animals
• Catalase (metabolism)
• Glutathione Peroxidase (metabolism)
• Hydrogen Peroxide (metabolism)
• Hyperbaric Oxygenation
• Lung (enzymology, metabolism)
• Myocardium (enzymology, metabolism)
• Oxygen Consumption
• Ranidae
• Thiobarbiturates (metabolism)
• Triazoles (pharmacology)