Imidazolium salts as innovative agents against Leishmania amazonensis

The available chemotherapeutic drugs for the treatment of leishmaniasis present problems relating to efficacy, emergence of parasite resistance, and adverse effects and cost. Azole antifungal drugs have been repurposed for this proposition but the clinical response has been variable. In this sense,...

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Veröffentlicht in:International immunopharmacology 2018-10, Vol.63, p.101-109
Hauptverfasser: Martins, Raísha Costa, Dorneles, Gilson Pires, Teixeira, Vivian Oliveira Nunes, Antonello, Ana Maria, Couto, Júlia Lacerda, Rodrigues Júnior, Luiz Carlos, Monteiro, Marta Chagas, Peres, Alessandra, Schrekker, Henri Stephan, Romão, Pedro Roosevelt Torres
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Sprache:eng
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Zusammenfassung:The available chemotherapeutic drugs for the treatment of leishmaniasis present problems relating to efficacy, emergence of parasite resistance, and adverse effects and cost. Azole antifungal drugs have been repurposed for this proposition but the clinical response has been variable. In this sense, this study assessed the leishmanicidal and immunomodulatory activities of azoles-derived imidazolium salts (IS), being the ionic imidazole-derived equivalents: 1-n-butyl-3-methylimidazolium chloride (C4MImCl), 1-n-decyl-3-methylimidazolium chloride (C10MImCl), 1-n-hexadecyl-3-methylimidazolium chloride (C16MImCl), 1-n-hexadecyl-3-methylimidazolium methanesulfonate (C16MImMeS), 1-n-hexadecyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (C16MImNTf2) and 1-methyl-3-n-octadecylimidazolium chloride (C18MImCl). Promastigotes of Leishmania amazonensis were incubated with IS at concentrations ranging from 0.1 to 100 μM, and the parasite survival was monitored. The effects of IS on reactive oxygen species (ROS) production and mitochondrial membrane potential of promastigotes, as well as on cytotoxicity against peripheral blood mononuclear cells (PBMC) and human erythrocytes were determined. Besides, the activities of IS against amastigotes and nitric oxide production were also evaluated. The IS inhibited parasite growth and showed potent leishmanicidal activity against promastigotes of L. amazonensis. In addition, IS induced mitochondrial dysfunction and ROS production in parasites, and presented low cytotoxicity against PBMC and human erythrocytes. Furthermore, at very low concentration (0.5 μM), C18MImCl, C16MImMeS, C16MImCl, C10MImCl and C16MImNTf2 were able to kill intramacrophage parasites at levels of 91.3, 100, 94.4, 95.3 and 35.6%, respectively. These results indicate that IS are promising candidates for the development of drugs against L. amazonensis. Graphical abstract [Display omitted] •Imidazolium salts showed potent activity against promastigotes and amastigotes of L. amazonensis.•Imidazolium salts present low cytotoxicity to mammalian cells and high parasite selectivity.•Imidazolium salts induced mitochondrial dysfunction and ROS in L. amazonensis.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2018.07.038