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<jats:title>SUMMARY</jats:title><jats:p>Chagas disease, which is caused by the parasite <jats:italic>Trypanosoma cruzi</jats:italic>, affects approximately 7–8 million people in Latin America. The drugs available to treat this disease are ineffective against chronic phase disease and are associated with toxic side effects. Therefore, the development of new compounds that can kill <jats:italic>T. cruzi</jats:italic> at low concentrations is critically important. Herein, we report the effects of a novel 3-arylideneindolin-2-one that inhibits sirtuins, which are highly conserved proteins that are involved in a variety of physiological processes. The compound KH-TFMDI was tested against the epimastigote, trypomastigote and amastigote forms of <jats:italic>T. cruzi</jats:italic>, and its effects were evaluated using flow cytometry, light and electron microscopy. KH-TFMDI inhibited the replication of <jats:italic>T. cruzi</jats:italic> intracellular amastigotes with an IC<jats:sub>50</jats:sub> of 0·5±0·2 <jats:italic>μ</jats:italic><jats:sc>m</jats:sc>, which is significantly lower than the IC<jats:sub>50</jats:sub> of benznidazole. The compound also lysed the highly infectious bloodstream trypomastigotes (BST) with LC<jats:sub>50</jats:sub> values of 0·8±0·3 <jats:italic>μ</jats:italic><jats:sc>m</jats:sc> at 4 °C and 2·5±1·1 <jats:italic>μ</jats:italic><jats:sc>m</jats:sc> at 37 °C. KH-TFMDI inhibited cytokinesis and induced several morphological changes in the parasite, leading to its death by apoptosis and autophagy. This study highlights sirtuins as a potential new target for Chagas disease therapy.</jats:p>

Original publication




Journal article




Cambridge University Press (CUP)

Publication Date





814 - 825