Deferoxamine improves antioxidative protection in the brain of neonatal rats: The role of anoxia and body temperature.

Neurosci Lett

N. Copernicus University, Department of Animal Physiology, Faculty of Biology and Environmental Protection, Lwowska 1 St., 87-100 Toruń, Poland. Electronic address:

Published: August 2016

After hypoxic-ischemic insult iron deposited in the brain catalyzes formation of reactive oxygen species. Newborn rats, showing reduced physiological body temperature and their hyperthermic counterparts injected with deferoxamine (DF), a chelator of iron, are protected both against iron-mediated neurotoxicity and against depletion of low-molecular antioxidants after perinatal asphyxia. Therefore, we decided to study the effects of DF on activity of antioxidant enzymes (superoxide dismutase-SOD, glutathione peroxidase-GPx and catalase-CAT) in the brain of rats exposed neonatally to a critical anoxia at body temperatures elevated to 39°C. Perinatal anoxia under hyperthermic conditions intensified oxidative stress and depleted the pool of antioxidant enzymes. Both the depletion of antioxidants and lipid peroxidation were prevented by post-anoxic DF injection. The present paper evidenced that deferoxamine may act by recovering of SOD, GPx and CAT activity to reduce anoxia-induced oxidative stress.

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http://dx.doi.org/10.1016/j.neulet.2016.06.022DOI Listing

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