Antileishmanial activity, cytotoxicity and cellular response of amphotericin B in combination with crotamine derived from Crotalus durissus terrificus venom using in vitro and in silico approaches

To investigate the in vitro activity, synergism, cytotoxicity and cellular immunological response, as well as the molecular affinity between amphotericin B (AmB) and crotamine (CTA), derived from Crotalus durissus terrificus venom against Leishmania amazonensis. This study performed the inhibition o...

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Veröffentlicht in:Toxicon (Oxford) 2022-10, Vol.217, p.96-106
Hauptverfasser: Valentim-Silva, João R., de Barros, Neuza B., Macedo, Sharon R.A., Ferreira, Amália dos S., Silva, Rodrigo S., Dill, Leandro S.M., Zanchi, Fernando B., do Nascimento, Johnny R., do Nascimento, Flávia R.F., Lourenzoni, Marcos R., Soares, Andreimar M., Calderon, Leonardo de A., Nicolete, Roberto
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Sprache:eng
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Zusammenfassung:To investigate the in vitro activity, synergism, cytotoxicity and cellular immunological response, as well as the molecular affinity between amphotericin B (AmB) and crotamine (CTA), derived from Crotalus durissus terrificus venom against Leishmania amazonensis. This study performed the inhibition of promastigotes and amastigotes’ growth under different concentrations of the drug and pharmacological combinations (AmB + CTA) based on the Berimbaum method (synergism study). The lactate dehydrogenase (LDH) quantification method was used to determine the cytotoxicity of the drug and combinations employing four cell lines (J774, HepG2, VERO, and C2C12). Following, the levels of Tumour Necrose Factor-alpha (TNF-α) and Interleukin-12 (IL-12) cytokines, using enzyme-linked immunosorbent assay (ELISA) and nitrites, as an indirect measure of Nitric Oxide (NO), using the Griess reaction were assessed in the supernatants of infected macrophages. In silico approach (molecular docking and dynamics) and binding affinity (surface plasmon resonance) between the drug and toxin were also investigated. CTA enhanced AmB effect against promastigote and amastigote forms of L. amazonensis, decreased the drug toxicity in different cell lines and induced the production of important Th1-like cytokines and NO by infected macrophages. The pharmacological combination also displayed consistent molecular interactions with low energy of coupling and a concentration-dependent profile. Our data suggest that this pharmacological approach is a promising alternative treatment against L. amazonensis infection due to the improved activity (synergistic effect) achieved against the parasites’ forms and to the decreased cytotoxic effect. [Display omitted] •Amphotericin B combined with crotamine displays a synergistic effect against promastigotes of L. amazonensis.•Amphotericin B cytotoxicity was decreased in different cell lines when combined with crotamine.•The pharmacological combination increases cytokines and nitric oxide productions by L. amazonensis-infected macrophages.•The combination between amphotericin B and crotamine displays consistent molecular interaction and binding affinit.
ISSN:0041-0101
1879-3150
DOI:10.1016/j.toxicon.2022.08.009