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

被引:9
作者
Francisco, Amanda Fortes [1 ]
de Abreu Vieira, Paula Melo [1 ]
Arantes, Jerusa Marilda [3 ]
Silva, Maisa [2 ]
Pedrosa, Maria Lucia [2 ]
Eloi-Santos, Silvana Maria [4 ]
Martins-Filho, Olindo Assis [3 ]
Teixeira-Carvalho, Andrea [3 ]
Silva Araujo, Marcio Sobreira [3 ]
Tafuri, Washington Luiz [1 ]
Carneiro, Claudia Martins [1 ,5 ]
机构
[1] Univ Fed Ouro Preto, ICEB, Nucleo Pesquisas Ciencias Biol, Lab Imunopatol, BR-35400000 Ouro Preto, MG, Brazil
[2] Univ Fed Ouro Preto, ICEB, Nucleo Pesquisas Ciencias Biol, Lab Bioquim & Biol Mol, BR-35400000 Ouro Preto, MG, Brazil
[3] Fundacao Osvaldo Cruz, Ctr Pesquisas Rene Rachou, Lab Biomarcadores Diagnost & Monitoracao, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Fac Med, Dept Propedeut Complementar, Belo Horizonte, MG, Brazil
[5] Univ Fed Ouro Preto, Escola Farm, Dept Anal Clin, BR-35400000 Ouro Preto, MG, Brazil
关键词
desferrioxamine; oxidative stress; Chagas' disease; Trypanosoma cruzi; IRON CHELATOR DESFERRIOXAMINE; TRYPANOSOMA-CRUZI; STRAINS;
D O I
10.1179/174329210X12650506623528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:185 / 190
页数:6
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