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Increase of reactive oxygen species by desferrioxamine during experimental Chagas' disease

Oxidative stress is common in inflammatory processes associated with many diseases including Chagas' disease. The aim of the present study was to evaluate, in a murine model, biomarkers of oxidative stress together with components of the antioxidant system in order to provide an overview of the...

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Detalles Bibliográficos
Autores principales: Francisco, Amanda Fortes, de Abreu Vieira, Paula Melo, Arantes, Jerusa Marilda, Silva, Maisa, Pedrosa, Maria Lúcia, Elói-Santos, Silvana Maria, Martins-Filho, Olindo Assis, Teixeira-Carvalho, Andréa, Araújo, Márcio Sobreira Silva, Tafuri, Washington Luiz, Carneiro, Cláudia Martins
Formato: Texto
Lenguaje:English
Publicado: Taylor & Francis 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955510/
https://www.ncbi.nlm.nih.gov/pubmed/20663295
http://dx.doi.org/10.1179/174329210X12650506623528
Descripción
Sumario:Oxidative stress is common in inflammatory processes associated with many diseases including Chagas' disease. The aim of the present study was to evaluate, in a murine model, biomarkers of oxidative stress together with components of the antioxidant system in order to provide an overview of the mechanism of action of the iron chelator desferrioxamine (DFO). The study population comprised 48 male Swiss mice, half of which were treated daily by intraperitoneal injection of DFO over a 35-day period, while half were administered sterile water in a similar manner. On the 14th day of the experiment, 12 DFO-treated mice and an equal number of untreated mice were experimentally infected with Trypanosoma cruzi. Serum concentrations of nitric oxide and superoxide dismutase and hepatic levels of total glutathione, thiobarbituric acid reactive species and protein carbonyl, were determined on days 0, 7, 14 and 21 post-infection. The results obtained revealed that DFO enhances antioxidant activity in the host but also increases oxidative stress, indicating that the mode of action of the drug involves a positive contribution to the host together with an effect that is not beneficial to the parasite.