Departamento de Bioquímica, Centro de Biociências, Universidade Federal de Pernambuco, Avenida Prof. Moraes Rego, 1235, Cidade Universitária. CEP 50.670-901, Recife, PE, Brazil; Departamento de Biofísica e Radiobiologia, Centro de Biociência, Universidade Federal de Pernambuco, Avenida Prof. Artur de Sá, s/n, Cidade Universitária. CEP 54740-520, Recife, PE, Brazil.
Departamento de Medicina Tropical, Centro de Ciências da Saúde, Universidade Federal de Pernambuco, Avenida Prof. Moraes Rego, s/n, Cidade Universitária, 50740-600, Recife, PE, Brazil; Laboratório de Imunopatologia Keizo Asami (LIKA), Universidade Federal de Pernambuco, Avenida Prof. Moraes Rego, 1235, Cidade Universitária. CEP 50.670-901, Recife, PE, Brazil.
Acta Trop. 2021 Oct;222:106044. doi: 10.1016/j.actatropica.2021.106044. Epub 2021 Jul 15.
In this study we evaluated the in vitro effect of divaricatic acid against coupled worms of Schistosoma mansoni. The schistosomicidal effect was evaluated through the bioassay of motility and mortality, cellular viability of the worms and ultrastructural analysis through Scanning Electron Microscopy. To evaluate the cytotoxicity of divaricatic acid, a cell viability assay was performed with human peripheral blood mononuclear cells. Divaricatic acid proved effect against S. mansoni after 3 hours of exposure. At the end of 24 h the concentrations of 100 - 200 μM presented lethality to the worms. Motility changes were observed at sublethal concentrations. The IC obtained by the cell viability assay for S. mansoni was 100.6 μM (96.24 - 105.2 μM). Extensive damage to the worm's tegument was observed such as peeling, erosion, bubbles, edema, damage and loss of tubercles and spines, fissures and tissue ruptures. No cytotoxicity was observed in human peripheral blood mononuclear cells. This report provides data showing the schistosomicidal effect of divaricatic acid on S. mansoni, causing death, motile changes and ultrastructural damage to worms. In addition, divaricatic acid was shown to be non-toxic to human peripheral blood mononuclear cells at concentrations effective on S. mansoni.
在这项研究中,我们评估了裂环酸对曼氏血吸虫耦合虫的体外作用。通过运动和死亡率的生物测定、虫体细胞活力和扫描电子显微镜的超微结构分析来评估杀血吸虫效果。为了评估裂环酸的细胞毒性,用人外周血单核细胞进行了细胞活力测定。裂环酸在暴露 3 小时后对 S. mansoni 有效。在 24 小时结束时,100-200μM 的浓度对虫体具有致死性。在亚致死浓度下观察到运动变化。细胞活力测定法得到的裂环酸对 S. mansoni 的 IC 为 100.6μM(96.24-105.2μM)。观察到虫体的表皮广泛受损,如剥落、侵蚀、气泡、水肿、损伤和结节和刺突丢失、裂缝和组织破裂。人外周血单核细胞未观察到细胞毒性。本报告提供的数据表明裂环酸对 S. mansoni 具有杀血吸虫作用,导致虫体死亡、运动变化和超微结构损伤。此外,裂环酸在有效浓度下对人外周血单核细胞显示出非毒性。