IF - Trabalhos de Conclusão de Curso

URI Permanente para esta coleção

http://200.137.215.59//handle/ri/1361

Navegar

Navegando IF - Trabalhos de Conclusão de Curso por Assunto "Amphotericin B"

Agora exibindo 1 - 1 de 1
  • Nenhuma Miniatura disponível
    Item
    Mecanismos de ação das atividades leishmanicidas da anfotericina B e miltefosina
    (Universidade Federal de Goiás, 2024-02-07) Silva, David de Ribamar Antunes da; Alonso, Antonio; Alonso, Antonio; Vieira, Sílvio Leão; Itikawa, Emerson Nobuyuki
    Leishmaniasis is a disease caused by parasites of the genus Leishmania, and its treatment involves the use of medications, with meglumine antimoniate, amphotericin B (AmB), and miltefosine (MTF) being the preferred choices according to health department guidelines. Electron paramagnetic resonance (RPE) spectroscopy with spin labels was employed to demonstrate that the drugs MTF and AmB induce rigidity in the membrane of the L. amazonensis parasite. Membrane rigidity was associated with lipid peroxidation and/or oxidation of membrane proteins, resulting from an increase in the formation of reactive oxygen species (ROS) promoted by the medications. Similar tests were conducted on J774A.1 macrophages, but membrane rigidity was not observed, suggesting that their production of nitric oxide (NO) may reduce oxidative stress. For MTF, membrane rigidity in Leishmania is not the result of its direct interactions with the membrane because immediately after treatment, MTF induces fluidity. For measurements immediately after treatment, where the incubation period is insufficient for oxidative stress to occur, AmB also induces membrane rigidity, but this effect was observed at a drug concentration 100 times higher. This result indicates that for higher concentrations of AmB, EPR spectroscopy can detect direct interactions of AmB with the parasite membrane, probably forming putative AmB/ergosterol aggregates that cause membrane rigidity. In J774A.1 macrophages, the effects of MTF-induced fluidity and AmB-induced rigidity were also observed. These effects occurred for short incubation periods and at the respective drug concentrations that showed cytotoxicity. Our studies have shown that these drugs act on the membrane and suggest that the mechanisms of action of their antileishmanial activities are associated with their primary effects on the cell membrane. Membrane alteration can cause ionic imbalance, which may affect mitochondrial membrane potential and, thus, increase ROS formation.