Programa de Pós-graduação em Ciências Biológicas, Universidade Estadual de Maringá, Av. Colombo 5790, CEP 87020-900, Maringá, Paraná, Brazil.
Programa de Pós-graduação em Ciências Farmacêuticas, Universidade Estadual de Maringá, Av. Colombo 5790, CEP 87020-900, Maringá, Paraná, Brazil.
Microbes Infect. 2016 Dec;18(12):787-797. doi: 10.1016/j.micinf.2016.07.007. Epub 2016 Jul 30.
This work evaluated the in vitro and in vivo activity of TDZ 2 on Trypanosoma cruzi amastigotes and determined the possible mechanism of action of this compound on T. cruzi death. TDZ 2 inhibited T. cruzi proliferation in vitro and had low haemolytic potential. It also induced morphological and ultrastructural alterations. We observed a reduction of cell volume, the depolarization of the mitochondrial membrane, an increase in ROS production, lipoperoxidation of the cell membrane, lipid bodies formation and production of nitric oxide, a decrease in reduced thiols levels and, presence of autophagic vacuoles. The in vivo study found a reduction of parasitemia in animals treated with TDZ 2 alone or combined with benznidazole. Altogether, the alterations induced by TDZ 2 point to an oxidative stress condition that lead to T. cruzi cell death.
本研究评估了 TDZ2 对 Trypanosoma cruzi 无鞭毛体的体外和体内活性,并确定了该化合物对 T. cruzi 死亡的可能作用机制。TDZ2 抑制了 T. cruzi 的体外增殖,且溶血潜能较低。它还诱导了形态和超微结构的改变。我们观察到细胞体积减小,线粒体膜去极化,ROS 产生增加,细胞膜脂质过氧化,脂滴形成和一氧化氮产生,还原型硫醇水平降低,自噬小体存在。体内研究发现,单独使用 TDZ2 或与苯并硝唑联合治疗的动物的寄生虫血症减少。总之,TDZ2 诱导的改变表明存在氧化应激状态,导致 T. cruzi 细胞死亡。