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Título

Acrylonitrile derivatives: In vitro activity and mechanism of cell death induction against Trypanosoma cruzi and Leishmania amazonensis

AutorBethencourt-Estrella, Carlos J.; Delgado-Hernández, Samuel CSIC ORCID; López-Arencibia, Atteneri; San Nicolás-Hernández, Desirée; Salazar-Villatoro, Lizbeth; Omaña-Molina, Maritza; Tejedor, David CSIC ORCID CVN ; García-Tellado, Fernando CSIC ORCID ; Lorenzo-Morales, Jacob; Piñero, José E.
Palabras claveChemotherapy
toxicity
PCD
Leishmaniasis
Chagas
acrylonitriles
Tesauro UNESCOCells
Fecha de publicación6-mar-2024
EditorElsevier BV
CitaciónInternational Journal for Parasitology: Drugs and Drug Resistance, 24, 100531: 1-11 (2024)
ResumenLeishmaniasis and Chagas disease are parasitic infections that affect millions of people worldwide, producing thousands of deaths per year. The current treatments against these pathologies are not totally effective and produce some side effects in the patients. Acrylonitrile derivatives are a group of compounds that have shown activity against these two diseases. In this work, four novels synthetic acrylonitriles were evaluated against the intracellular form and extracellular forms of L. amazonensis and T. cruzi. The compounds 2 and 3 demonstrate to have good selectivity indexes against both parasites, specifically the compound 3 against the amastigote form (SI = 6 against L. amazonensis and SI = 7.4 against T. cruzi). In addition, the parasites treated with these two compounds demonstrate to produce a programmed cell death, since they were positive for the events studied related to this type of death, including chromatin condensation, accumulation of reactive oxygen species and alteration of the mitochondrial membrane potential. In conclusion, this work confirms that acrylonitriles is a source of possible new compounds against kinetoplastids, however, more studies are needed to corroborate this activity.
Versión del editorhttps://doi.org/10.1016/j.ijpddr.2024.100531
URIhttp://hdl.handle.net/10261/352759
DOI10.1016/j.ijpddr.2024.100531
E-ISSN2211-3207
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