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Relative activity of triclabendazole metabolites against the liver fluke, Fasciola hepatica

机译:三氯苯达唑代谢物对肝吸虫Fasciola hepatica的相对活性

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A study has been carried out to determine the relative activity of triclabendazole (TCBZ) and its sulphoxide (TCBZSO) and sulphone (TCBZSO(2)) metabolites against the adult stage of the liver fluke, Fasciola hepatica. Flukes were incubated for 24h in vitro in 15mug/ml of each of the compounds and prepared for scanning and transmission electron microscopy. All three compounds induced changes to the surface morphology of the fluke, the changes comprising swelling and blebbing to a greater or lesser extent in different regions of the fluke. TCBZSO(2) was more disruptive anteriorly and TCBZSO posteriorly. Internal ultrastructural changes were evident following incubation with each of the compounds, with an order of severity TCBZSO(2)>TCBZSO>TCBZ. Swelling of the basal infolds and mitochondria were observed in the tegumental syncytium. In the tegumental cell bodies, there was a reduction in the number of secretory bodies, disruption of the Golgi complexes and swelling of the mitochondria. Severe flooding of the internal tissues was observed with TCBZSO(2) and, to a lesser extent, with TCBZSO and TCBZ. The results demonstrate that both TCBZ and TCBZSO(2) are capable of disrupting the fluke in vitro and are not the inactive compounds they were assumed to be previously. They may well contribute to drug action in vivo as well, indicating that drug action is due to the additive effects of several metabolites, rather than being due to a single active metabolite, namely, TCBZSO.
机译:已经进行了一项研究,以确定三氯苯达唑(TCBZ)及其亚砜(TCBZSO)和砜(TCBZSO(2))代谢产物对肝吸虫成年阶段Fasciola hepatica的相对活性。将薄片在每种化合物15mug / ml中孵育24小时,并准备进行扫描和透射电子显微镜检查。所有这三种化合物均引起了吸虫的表面形态变化,该变化包括在吸虫的不同区域或多或少地发生了溶胀和起泡。 TCBZSO(2)的破坏力更强,而TCBZSO的破坏力更强。与每种化合物一起孵育后,内部超微结构的变化很明显,其严重程度为TCBZSO(2)> TCBZSO> TCBZ。在被膜合胞体中观察到了基底内褶和线粒体的肿胀。在被膜细胞体中,分泌体的数量减少,高尔基体的破坏和线粒体的肿胀。 TCBZSO(2)观察到内部组织严重浸水,而TCBZSO和TCBZ观察到程度较小。结果表明,TCBZ和TCBZSO(2)都能够在体外破坏the虫,并且不是以前假定的无活性化合物。它们也可能很好地促进体内的药物作用,表明药物作用是由于几种代谢物的累加作用,而不是由于单一的活性代谢物,即TCBZSO。

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