Department of Veterinary Sciences, University of Pisa, viale delle Piagge 2, 56124 Pisa, Italy.
CREA Research Centre for Animal Production and Aquaculture; viale Piacenza 29, 26900 Lodi, Italy.
Molecules. 2020 Jan 7;25(2):242. doi: 10.3390/molecules25020242.
Gastrointestinal strongyle nematodes (GIS) are included among the most important parasites of small ruminants. The widespread drug resistance and drug residues in products of animal origin have increased the interest in the search for natural compounds with anthelmintic activity as a valid alternative to current synthetic drugs. The aim of the present investigation was to test the 'in vitro' anthelmintic activity of saponins and prosapogenins from different species, selected for their importance as a forage crop worldwide for animal feeding. From these plants, saponin mixtures were extracted, purified and used at scalar concentrations to evaluate their anthelmintic activities against sheep gastrointestinal strongyles (GISs), by the egg hatch test. Treated and untreated controls were used as the comparison. Data were statistically analyzed, and EC and EC were also calculated. All saponins and prosapogenins showed inhibiting effects on GIS eggs in a concentration-dependent manner. At higher concentrations, most of them showed an efficacy comparable to the reference drug (Thiabendazole 3 µg/mL) ( < 0.001). With 1.72 mg/mL EC and 3.84 mg/mL EC, saponin from cultivars Anglona was the most active. Obtained results encourage further studies aimed at evaluating the efficacy 'in vivo' of saponins which resulted as most effective 'in vitro' in this study.
胃肠道强线虫(GIS)是小反刍动物中最重要的寄生虫之一。由于在动物源性产品中广泛存在耐药性和药物残留问题,人们对寻找具有驱虫活性的天然化合物作为现有合成药物的有效替代品的兴趣日益增加。本研究旨在测试从不同物种中选择的皂苷和原皂苷的“体外”驱虫活性,这些物种因其作为全球动物饲料的饲料作物而具有重要意义。从这些植物中提取、纯化了皂苷混合物,并在标度浓度下使用,以通过卵孵化试验评估其对绵羊胃肠道强线虫(GIS)的驱虫活性。将处理过的和未处理的对照用作比较。对数据进行了统计分析,并计算了 EC 和 EC。所有皂苷和原皂苷均以浓度依赖的方式对 GIS 卵表现出抑制作用。在较高浓度下,它们中的大多数表现出与参考药物(噻苯达唑 3 µg/mL)相当的功效(<0.001)。在 1.72mg/mL 的 EC 和 3.84mg/mL 的 EC 下,Anglona 品种的皂苷活性最高。本研究中获得的结果鼓励进一步研究旨在评估在“体内”的有效性,这些皂苷在本研究中表现出最有效的“体外”活性。