2025-07-222025-07-222017FERNANDES, Kelly Souza et al. The cytotoxic activity of miltefosine against Leishmania and macrophages is associated with dynamic changes in plasma membrane proteins. Biochimica et Biophysica Acta (BBA) - Biomembranes, Amsterdam, v. 1859, n. 1, p. 1-9, 2016. DOI: 10.1016/j.bbamem.2016.10.008. Disponível em: https://www.sciencedirect.com/science/article/pii/S0005273616303352?via%3Dihub. Acesso em: 22 jul. 2025.e- 1879-26420005-2736https://repositorio.bc.ufg.br//handle/ri/28111In this study, we combined electron paramagnetic resonance (EPR) spectroscopy with an analysis of biophysical cellular parameters to study the mechanisms underlying the in vitro anti-leishmanial activity of miltefosine (MT). A thiol-specific spin label attached to membrane-bound proteins of Leishmania amazonensis and peritoneal mac rophages indicated that MT may bind to plasma membrane proteins in large quantities via a detergent-like action and cause structural changes associated with a marked increase in dynamics and exposure to an aqueous envi ronment. EPR spectra of a spin-labeled stearic acid indicated strong interactions between the probe and mem brane proteins and a marked increase in the membrane fluidity of MT-treated cells. The cytotoxicity of MT was found to depend on the cell concentration used in the assay. This dependence was described by an equation in volving the 50% inhibitory concentrations of MT in the aqueous medium (cw50) and the cell membrane (cm50) and the membrane-aqueous medium partition coefficient of MT (K). With a cw50 of 8.7 μM, macrophages were less sensitive to MT than amastigotes and promastigotes of Leishmania, which had cw50 values of 2.4–3.1 μM. The estimated cm50 of MT for Leishmania was 1.8 M, which appears sufficient to cause ruptures or formation of pores in the plasma membrane. Additionally, we demonstrated that the changes in the plasma membrane detect ed by EPR spectroscopy occurred at cytotoxic concentrations of MT, as assessed through in vitro assays.engAcesso Abertohttp://creativecommons.org/licenses/by-nc-nd/4.0/LeishmaniaMacrophagesMembrane fluidityProtein dynamicsMiltefosineArtigo10.1016/j.bbamem.2016.10.008