Abstract
The activity of an (8-hydroxymethylen)-trieicosanyl acetate compound obtained from chloroform extracts of Senna villosa (Mill.) H.S. Irwin & Barneby (Leguminosae) against Trypanosoma cruzi was evaluated in vivo. Oral doses of 2.1, 8.4, and 33.6 μg/g were tested for 28 days in BALB/c mice infected with T. cruzi. Reduced parasitemia levels of 70.5%, 73.8%, and 80.9%, respectively, were observed. A significant reduction in amastigote nests was detected in the cardiac tissue of treated animals at doses of 8.4 and 33.6 μg/g. The LD50 of (8-hydroxymethylen)-trieicosanyl acetate was impossible to determine because none of the animals died, even at oral doses of 5000 μg/g; consequently, it was impossible to determine the acute oral toxicity in vivo. © 2010 Informa UK Ltd.
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Jimenez-Coello, M., Acosta-Viana, K. Y., Guzman-Marin, E., Perez Gonzalez, C., & Salud Perez Gutierrez, M. (2010). Anti-trypanosomal activity of (8-hydroxymethylen)-trieicosanyl acetate against infective forms of Trypanosoma cruzi. Pharmaceutical Biology, 48(6), 666–671. https://doi.org/10.3109/13880200903241853
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