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Evaluation of Praziquantel effects on Echinostoma paraensei ultrastructure

机译:吡喹酮对副猪棘皮动物超微结构的影响

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摘要

Echinostomiasis is a food-borne, intestinal, zoonotic, snail-mediated helminthiasis caused by digenean trematodes of the family Echinostomatidae with seven species of the genus Echinostoma infecting humans or domestic and wildlife animals. Echinostomaparaensei is a peristomic 37-collar-spined echinostome belonging to the "revolutum group". Praziquantel (PZQ) is the drug of choice for treatment and control of human schistosomia-sis and food-borne trematodiasis. In the present study we used scanning and transmission electron microscopy to further elucidate the trematocidal effect of PZQ on adult E. paraense and confirmed that this trematode is a suitable model to study anthelmintic drugs. Hamsters infected with E. paraensei were treated with a singledose of 30 mg kg-1 of PZQ. The worms were recovered 15,30,90 and 180 min after drug administration. There was a significant decrease in worm burden in the small intestine in the hamster-]*, paraensei model at the intervals of30,90 and 180 min after thetreatment. The worms displayed damage of the peristomic collar with internalization of the spines and erosion of the tegument of the circu-moral head-collar of spines. Ultrastructural analysis demonstrated an intense vacuolization, of the tegument, appearance of autophagic vacuoles and swelling of the basal infolds of the tegumental syncytium. There was no change in the morphology of cells from the exnetory system of adult E. paraensei, however, there was an apparent decrease of stores of glycogen particles in parenchymal cells in PZQ-treated worms. Our results demonstrated that PZQ. promotes surface and ultrastructural damage of the tegument of adult E. paraensei supporting the idea that this trematode may constitute a good model to investigate drug effects mechanisms in vitro and in vivo.
机译:棘皮虫病是由食管mat科(Echinostomatidae)的双属吸虫引起的一种食源性,肠道,人畜共患病,由蜗牛介导的蠕虫病,它感染了人类或家养和野生动物七种棘皮动物。 Echinostomaparaensei是属于“ revolutum组”的蠕虫性37领棘突棘突动物。吡喹酮(PZQ)是用于治疗和控制人类血吸虫病和食源性皮肤病的首选药物。在本研究中,我们使用扫描电子显微镜和透射电子显微镜进一步阐明了PZQ对成年大肠杆菌的杀螨作用,并证实该杀螨剂是研究驱虫药的合适模型。用30 mg kg-1的PZQ单剂量处理感染副猪大肠杆菌的仓鼠。给药后15、30、90和180分钟恢复蠕虫。在处理后的30,90和180分钟的间隔内,仓鼠-* *旁侧模型的小肠蠕虫负担显着降低。蠕虫显示出棘突内部化和棘突的周围道德头环外皮被侵蚀而引起的蠕动环的损坏。超微结构分析显示出强烈的空泡化,外被膜,自噬泡的出现和外膜合胞体的基部肿胀。从成年副猪大肠杆菌的外泄系统中细胞的形态没有变化,但是,在经过PZQ处理的蠕虫中,实质细胞中糖原颗粒的储藏量明显减少。我们的结果证明了PZQ。促进成年大肠杆菌的外皮的表面和超微结构损伤,支持这种吸虫可能构成研究体内外药物作用机制的良好模型的观点。

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