| Literature DB >> 27297770 |
Hanna Kletkiewicz1, Anna Nowakowska2, Agnieszka Siejka3, Celestyna Mila-Kierzenkowska4, Alina Woźniak5, Michał Caputa6, Justyna Rogalska7.
Abstract
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.Entities:
Keywords: Antioxidant enzymes; Deferoxamine; Hyperthermia; Neonatal anoxia
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Year: 2016 PMID: 27297770 DOI: 10.1016/j.neulet.2016.06.022
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046