Effects of cyclooxygenase inhibitors on parasite burden, anemia and oxidative stress in murine Trypanosoma cruzi infection

被引:49
作者
Tatakihara, Vera L. Hideko [1 ]
Cecchini, Rubens [1 ]
Borges, Celso L. [2 ]
Malvezi, Aparecida D. [1 ]
Graca-de Souza, Viviane K. [3 ]
Yamada-Ogatta, Sueli F. [3 ]
Rizzo, Luiz V. [4 ]
Pinge-Filho, Phileno [1 ]
机构
[1] Univ Estadual Londrina, Dept Ciencias Patol, Ctr Ciencias Biol, BR-86051990 Londrina, Parana, Brazil
[2] Univ Estadual Ponta Grossa, Dept Analises Clin, Ponta Grossa, Parana, Brazil
[3] Univ Estadual Londrina, Dept Microbiol, Ctr Ciencias Biol, Londrina, Parana, Brazil
[4] Univ Sao Paulo, Dept Imunol, Sao Paulo, Brazil
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2008年 / 52卷 / 01期
关键词
Trypanosoma cruzi; Chagas' disease; cyclooxygenase; anemia; oxidative stress; nitric oxide;
D O I
10.1111/j.1574-695X.2007.00340.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prostaglandins are known to be produced by macrophages when challenged with Trypanosoma cruzi, the etiological agent of Chagas' disease. It is not known whether these lipid mediators play a role in oxidative stress in host defenses against this important protozoan parasite. In this study, we demonstrated that inducible cyclooxygenase-mediated prostaglandin production is a key chemical mediator in the control of parasite burden and erythrocyte oxidative stress during T. cruzi infection in C57BL/6 and BALB/c mice, prototype hosts for the study of resistance and susceptibility in murine Chagas' disease. The results suggested the existence of at least two mechanisms of oxidative stress, dependent or independent with regard to the nitric oxide and cyclooxygenase pathway, where one or the other is more evident depending on the mouse strain.
引用
收藏
页码:47 / 58
页数:12
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