Chalcone Derivative Induces Flagellar Disruption and Autophagic Phenotype in In Vitro.

Pathogens

Laboratório de Enzimologia, Departamento de Fisiologia, Universidade Federal de Sergipe, São Cristóvão 49100-000, SE, Brazil.

Published: March 2023

is a trypanosomatid phytoparasite, found in a great variety of species, including tomato plants. It is a significant problem for agriculture, causing high economic loss. In order to reduce the vegetal infections, different strategies have been used. The biological activity of molecules obtained from natural sources has been widely investigated to treat trypanosomatids infections. Among these compounds, chalcones have been shown to have anti-parasitic and anti-inflammatory effects, being described as having a remarkable activity on trypanosomatids, especially in species. Here, we evaluated the antiprotozoal activity of the chalcone derivative (NaF) on promastigotes, while also assessing its mechanism of action. The results showed that treatment with the derivative NaF for 24 h promotes an important reduction in the parasite proliferation (IC/24 h = 23.6 ± 4.6 µM). At IC/24 h concentration, the compound induced an increase in reactive oxygen species (ROS) production and a shortening of the unique flagellum of the parasites. Electron microscopy evaluation reinforced the flagellar phenotype in treated promastigotes, and a dilated flagellar pocket was frequently observed. The treatment also promoted a prominent autophagic phenotype. An increased number of autophagosomes were detected, presenting different levels of cargo degradation, endoplasmic reticulum profiles surrounding different cellular structures, and the presence of concentric membranar structures inside the mitochondrion. Chalcone derivatives may present an opportunity to develop a treatment for the infection, as they are easy to synthesize and are low in cost. In order to develop a new product, further studies are still necessary.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10051746PMC
http://dx.doi.org/10.3390/pathogens12030423DOI Listing

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