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首页> 外文期刊>International Journal for Parasitology: Drugs and Drug Resistance >In vitro and in vivo assessment of the effect of antiprotozoal compounds isolated from Psoralea corylifolia against Ichthyophthirius multifiliis in fish
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In vitro and in vivo assessment of the effect of antiprotozoal compounds isolated from Psoralea corylifolia against Ichthyophthirius multifiliis in fish

机译:分离自花粉补骨脂的抗原生动物化合物对鱼多丝鱼的效果的体外和体内评估

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Ichthyophthirius multifiliis, an external fish parasite, often causes significant economic damage to the aquaculture industry. Since the use of malachite green was banned, the search of alternative substance to control I.@?multifiliis infections becomes stringent. In present study, in vitro and in vivo anti-ich efficacies of isopsoralen and psoralidin, two active compounds isolated from methanol extract of Psoralea corylifolia by bioassay-guided fractionation based on the efficacy of anti-ich encysted tomonts, were evaluated. In vitro antiprotozoal efficacy of psoralidin is much better than that of isopsoralen. Psoralidin can kill all theronts at concentrations of 0.8@?mg/L or more during 4@?h exposure; and terminate reproduction of I.multifiliis post 6@?h exposure of protomonts to 0.9@?mg/L and encysted tomonts to 1.2@?mg/L. In vivo trials showed that 5@?h exposure of infected fish to 2.5@?mg/L of psoralidin significantly reduced the number of theronts released from tomonts. Furthermore, we observed that a part of protomonts, collected from infected fish post treatment, presented characteristic morphological changes of apoptosis after staining with Annexin V-EGFP/propidium iodide, indicating the possible mechanism of psoralidin against I.multifiliis trophont in situ. On the basis of these results, psoralidin can be used as a potential lead compound for the development of commercial drug against I.multifiliis.
机译:鱼类Ichthyophthirius multifiliis是一种外部鱼类寄生虫,经常对水产养殖业造成重大经济损失。由于孔雀石绿的使用被禁止,因此寻找控制I. @多菌丝感染的替代物质变得很严格。在本研究中,评估了异补骨脂素和补骨脂素的体外和体内抗-ich功效,基于抗-ich-ted tomonts的功效,通过生物测定指导分级分离了从补骨脂的甲醇提取物中分离的两种活性化合物。补骨脂素在体外的抗原生动物功效远优于异补骨脂素。补骨脂素可以在4小时暴露期间杀死所有浓度在0.8@?mg/L或更高的强效药。并终止原虫6 @ h h暴露于0.9@?mg/L并诱使tomonts暴露于1.2@?mg/L的多菌I.繁殖。体内试验表明,受感染鱼在5?h暴露于2.5@?mg/L补骨脂素的作用显着减少了从tomonts释放的火药数量。此外,我们观察到,用膜联蛋白V-EGFP /碘化丙锭染色后,从感染鱼的处理后收集的一部分原峰表现出凋亡的特征性形态变化,表明补骨脂素原位抵抗多丝衣原体的可能机制。基于这些结果,补骨脂素可以用作潜在的领先化合物,用于开发抗多丝酵母的商业药物。

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