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Pereira, Vinícius R. D.; Junior, Ismael J. Alves; da Silveira, Lígia S.; Geraldo, Reinaldo B.; de F. Pinto, Priscila; Teixeira, Fernanda S.; Salvadori, Maria C.; Silva, Marcos P.; Alves, Lara A.; Capriles, Priscila V. S. Z.; das C. Almeida, Ayla; Coimbra, Elaine S.; Pinto, Pedro L. S.; Couri, Mara R. C.; de Moraes, Josué; Da Silva Filho, Ademar A.
Chemistry & biodiversity, December 2018, Letnik: 15, Številka: 12Journal Article
In this study, we evaluated the in vitro and in vivo schistosomicidal activities of chalcones against Schistosoma mansoni worms. In vitro assays revealed that chalcones 1 and 3 were the most active compounds, without affecting significantly mammalian cells. Confocal laser scanning microscopy and scanning electron microscopy studies revealed reduction on the numbers of tubercles and morphological alterations in the tegument of S. mansoni worms after in vitro incubation with chalcones 1 and 3. In a mouse model of schistosomiasis, the oral treatment (400 mg/kg) with chalcone 1 or 3 significantly caused a total worm burden reduction in mice. Chalcone 1 showed significant inhibition of the S. mansoni ATP diphosphohydrolase activity, which was corroborated by molecular docking studies. The results suggested that chalcones could be explored as lead compounds with antischistosomal properties.
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