Leishmania amazonensis trypanothione reductase:: Evaluation of the effect of glutathione analogs on parasite growth, infectivity and enzyme activity

被引:13
|
作者
Castro-Pinto, Denise Barcante
Lima, Edson L. Silva
Cunha, Andrea S.
Genestra, Marcelo
De Leo, Rosa Maria
Monteiro, Fabiane
Leon, Leonor L. [1 ]
机构
[1] Fiocruz MS, Oswaldo Cruz Fdn, Inst Oswaldo Cruz, Dept Immunol, BR-21045900 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Dept Chem, Rio De Janeiro, Brazil
关键词
trypanothione; trypanothione reductase; Leishmania amazonensis; glutathione analogs;
D O I
10.1080/14756360600920180
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
Trypanothione reductase (TR) is a major enzyme in trypanosomatids. Its substrate, trypanothione is a molecule containing a tripeptide (L-glutamic acid-cysteine-glycine) coupled to a polyamine, spermidine. This redox system (TR/Trypanothione) is vital for parasite survival within the host cell and has been described as a good target for chemotherapy anti-Leishmania. The use of tripeptides analogs of glutathione would result in a decrease in trypanothione synthesis and as a consequence in TR activity. In this work, besides the enzyme potential inhibition, it also evaluated the influence of those analogs on parasite growth and on its infective capacity. The results showed a significant effect on parasite growth and infectivity and in addition TR activity was highly inhibited. These results are very promising, suggesting a potential use of those analogs as therapeutic drugs against experimental diseases caused by trypanosomatids.
引用
收藏
页码:71 / 75
页数:5
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